View Future GrowthCentessa Pharmaceuticals 過去の業績過去 基準チェック /06Centessa Pharmaceuticalsは6.7%の年平均成長率で業績を伸ばしているが、Biotechs業界はgrowingで33.8%毎年増加している。売上は成長しており、年平均64.7%の割合である。主要情報6.70%収益成長率21.96%EPS成長率Biotechs 業界の成長17.04%収益成長率64.70%株主資本利益率-51.43%ネット・マージンn/a前回の決算情報31 Mar 2026最近の業績更新更新なしすべての更新を表示Recent updatesNew Risk • May 06New major risk - Revenue sizeThe company makes less than US$1m in revenue. This is considered a major risk. Companies with a small amount of revenue are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$145m net loss in 3 years). Share price has been volatile over the past 3 months (14% average weekly change). Shareholders have been diluted in the past year (16% increase in shares outstanding). Significant insider selling over the past 3 months (US$2.2m sold).お知らせ • May 04Centessa Pharmaceuticals plc, Annual General Meeting, Jun 12, 2026Centessa Pharmaceuticals plc, Annual General Meeting, Jun 12, 2026. Location: sancroft, 10-15 newgate street, ec1a 7az, london United KingdomNew Risk • Apr 02New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 16% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$216m net loss in 3 years). Share price has been volatile over the past 3 months (14% average weekly change). Shareholders have been diluted in the past year (16% increase in shares outstanding). Significant insider selling over the past 3 months (US$3.2m sold).New Risk • Mar 31New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of American stocks, typically moving 6.5% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$203m net loss in 3 years). Share price has been volatile over the past 3 months (6.5% average weekly change). Significant insider selling over the past 3 months (US$3.2m sold).Price Target Changed • Mar 31Price target increased by 8.0% to US$42.36Up from US$39.23, the current price target is an average from 10 analysts. New target price is 6.7% above last closing price of US$39.71. The company is forecast to post a net loss per share of US$1.38 next year compared to a net loss per share of US$2.06 last year.お知らせ • Mar 31Eli Lilly and Company (NYSE:LLY) entered into a definitive agreement to acquire Centessa Pharmaceuticals plc (NasdaqGS:CNTA) from Medicxi Ventures (UK) LLP, Index Ventures SA, General Atlantic Service Company, L.P. and other shareholders for $5.6 billion.Eli Lilly and Company (NYSE:LLY) entered into a definitive agreement to acquire Centessa Pharmaceuticals plc (NasdaqGS:CNTA) from Medicxi Ventures (UK) LLP, Index Ventures SA, General Atlantic Service Company, L.P. and other shareholders for $5.6 billion on March 31, 2026. Under the terms of the transaction agreement, Eli Lilly will acquire all of the issued and to be issued share capital of Centessa (including the American Depositary Shares (ADSs) representing ordinary shares) for $38.00 in cash per share plus one non-transferrable contingent value right (CVR) that entitles the holder to receive up to an aggregate of $9.00 subject to the achievement of three milestones described below, for total potential aggregate per share consideration of up to $47.00. CVR holders would become entitled to receive contingent payments as follows: (i) $2.00 per CVR in cash, upon U.S. FDA approval of cleminorexton (formerly ORX750) or ORX142 for the treatment of narcolepsy type 2 prior to the fifth anniversary of transaction closing; (ii) $5.00 per CVR in cash, upon U.S. FDA approval of cleminorexton (formerly ORX750) or ORX142 for the treatment of idiopathic hypersomnia prior to the fifth anniversary of transaction closing; and (iii) $2.00 per CVR in cash, upon the first U.S. FDA approval of cleminorexton (formerly ORX750) or ORX142 for the treatment of any indication prior to January 1, 2030. The agreement stipulates a $63.06 million termination fee payable by the target to the buyer. Entities affiliated with Medicxi Ventures, entities affiliated with Index Ventures, and affiliates of General Atlantic have signed voting and support agreements whereby they agree to vote to approve the transaction. The shares subject to the agreements represent a total of approximately 24.1% of Centessa’s outstanding ordinary shares (represented by ADSs). The transaction, which will be effectuated by way of a scheme of arrangement under the laws of England and Wales, subject to approval by Centessa shareholders, sanction by the High Court of Justice of England and Wales and satisfaction of other customary closing conditions, including regulatory and antitrust approvals. The boards of directors of both companies have approved the transaction. The transaction is expected to close in the third quarter of 2026. Morgan Stanley & Co. LLC acted as financial advisor for Eli Lilly and Company. Sarkis Jebejian, Keri Schick Norton, Steven M. Choi of Kirkland & Ellis LLP and Dipak Bhundia, Bonian Wu of Kirkland & Ellis International LLP acted as legal advisor for Eli Lilly and Company. Centerview Partners LLC and Jefferies LLC acted as financial advisors for Centessa Pharmaceuticals plc. Stuart M Cable, Lisa R Haddad, Blake Liggio of Goodwin Procter LLP acted as legal advisor for Centessa Pharmaceuticals plc.Recent Insider Transactions Derivative • Mar 29Chief People Officer notifies of intention to sell stockKaren Anderson intends to sell 41k shares in the next 90 days after lodging an Intent To Sell Form on the 26th of March. If the sale is conducted around the recent share price of US$28.15, it would amount to US$1.2m. Since June 2025, Karen's direct individual holding has increased from 58.36k shares to 66.12k. Company insiders have collectively sold US$12m more than they bought, via options and on-market transactions in the last 12 months.Recent Insider Transactions Derivative • Mar 15Chief People Officer notifies of intention to sell stockKaren Anderson intends to sell 120k shares in the next 90 days after lodging an Intent To Sell Form on the 13th of March. If the sale is conducted around the recent share price of US$25.86, it would amount to US$3.1m. Since June 2025, Karen's direct individual holding has increased from 58.36k shares to 76.75k. Company insiders have collectively sold US$8.6m more than they bought, via options and on-market transactions in the last 12 months.Recent Insider Transactions • Feb 04General Counsel recently sold US$1.0m worth of stockOn the 2nd of February, Iqbal Hussain sold around 40k shares on-market at roughly US$25.15 per share. This transaction amounted to 61% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Insiders have been net sellers, collectively disposing of US$3.6m more than they bought in the last 12 months.お知らせ • Dec 13+ 1 more updateCentessa Pharmaceuticals plc Announces CEO Changes, Effective January 1, 2026Centessa Pharmaceuticals plc announced that its Board of Directors has appointed Mario Alberto Accardi PhD, President and founder of Centessa’s Orexin Program, as Chief Executive Officer (CEO), effective January 1, 2026. Dr. Accardi will succeed Saurabh Saha MD PhD, who will step down from his position as CEO, effective January 1, 2026. Dr. Saha will be appointed advisor to the CEO. As President of Centessa’s Orexin Program, Dr. Accardi has been responsible for leading the advancement of the orexin pipeline, which has become the full focus of the Company. Prior to Centessa, he was founder and CEO of Orexia Therapeutics. At Orexia, he successfully raised a €40M Series A, established multiple strategic partnerships, and led the company through its successful acquisition by Centessa in 2021. Dr. Accardi holds a Postgraduate in Genomic Medicine, a PhD in Biomedical Engineering and a First-Class Honours MEng Degree in Mechanical Engineering from Imperial College London.Price Target Changed • Nov 20Price target increased by 7.3% to US$36.38Up from US$33.92, the current price target is an average from 13 analysts. New target price is 32% above last closing price of US$27.54. Stock is up 51% over the past year. The company is forecast to post a net loss per share of US$1.38 next year compared to a net loss per share of US$2.06 last year.Recent Insider Transactions Derivative • Nov 16Chief Technology & Quality Officer exercised options and sold US$663k worth of stockOn the 12th of November, Tia Bush exercised 40k options at a strike price of around US$9.42 and sold these shares for an average price of US$26.00 per share. This trade did not impact their existing holding. Since December 2024, Tia's direct individual holding has decreased from 76.05k shares to 74.53k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.お知らせ • Nov 12+ 1 more updateCentessa Pharmaceuticals plc has completed a Follow-on Equity Offering in the amount of $250.000001 million.Centessa Pharmaceuticals plc has completed a Follow-on Equity Offering in the amount of $250.000001 million. Security Name: American Depositary Shares Security Type: Depositary Receipt (Common Stock) Securities Offered: 11,627,907 Price\Range: $21.5 Discount Per Security: $1.29分析記事 • Oct 28Health Check: How Prudently Does Centessa Pharmaceuticals (NASDAQ:CNTA) Use Debt?Howard Marks put it nicely when he said that, rather than worrying about share price volatility, 'The possibility of...Buy Or Sell Opportunity • Sep 30Now 20% undervaluedOver the last 90 days, the stock has risen 76% to US$24.25. The fair value is estimated to be US$30.41, however this is not to be taken as a buy recommendation but rather should be used as a guide only. Revenue has grown by 102% over the last 3 years. Earnings per share has grown by 13%. For the next 3 years, revenue is forecast to grow by 73% per annum. Earnings are also forecast to grow by 24% per annum over the same time period.Recent Insider Transactions Derivative • Sep 26Chief Technology & Quality Officer exercised options and sold US$510k worth of stockOn the 24th of September, Tia Bush exercised 35k options at a strike price of around US$9.42 and sold these shares for an average price of US$24.00 per share. This trade did not impact their existing holding. Since September 2024, Tia's direct individual holding has decreased from 78.08k shares to 74.53k. Company insiders have collectively sold US$15m more than they bought, via options and on-market transactions in the last 12 months.Recent Insider Transactions Derivative • Sep 14Chief Technology & Quality Officer exercised options and sold US$612k worth of stockOn the 10th of September, Tia Bush exercised 50k options at a strike price of around US$8.01 and sold these shares for an average price of US$20.30 per share. This trade did not impact their existing holding. Since September 2024, Tia's direct individual holding has decreased from 78.08k shares to 74.53k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.Buy Or Sell Opportunity • Jul 31Now 23% overvalued after recent price riseOver the last 90 days, the stock has risen 26% to US$17.17. The fair value is estimated to be US$13.97, however this is not to be taken as a sell recommendation but rather should be used as a guide only. Revenue has grown by 107% over the last 3 years. Earnings per share has grown by 14%. For the next 3 years, revenue is forecast to grow by 67% per annum. Earnings are also forecast to grow by 21% per annum over the same time period.Recent Insider Transactions Derivative • Jul 23CEO & Director exercised options and sold US$664k worth of stockOn the 21st of July, Saurabh Saha exercised 55k options at a strike price of around US$3.85 and sold these shares for an average price of US$15.92 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 12% salary and 88% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since September 2024, Saurabh's direct individual holding has decreased from 345.91k shares to 90.33k. Company insiders have collectively sold US$15m more than they bought, via options and on-market transactions in the last 12 months.分析記事 • Jul 17Centessa Pharmaceuticals (NASDAQ:CNTA) Is Using Debt SafelyLegendary fund manager Li Lu (who Charlie Munger backed) once said, 'The biggest investment risk is not the volatility...Recent Insider Transactions Derivative • Jun 22CEO & Director exercised options and sold US$483k worth of stockOn the 20th of June, Saurabh Saha exercised 55k options at a strike price of around US$3.85 and sold these shares for an average price of US$12.63 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 12% salary and 88% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since June 2024, Saurabh's direct individual holding has decreased from 417.17k shares to 90.33k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.お知らせ • Jun 18Centessa Pharmaceuticals plc Announces Clearance of Investigational New Drug Application for ORX142Centessa Pharmaceuticals plc announced that the U.S. Food and Drug Administration (FDA) has cleared the IND to initiate a Phase 1 clinical study of ORX142 in healthy volunteers. ORX142 is an investigational, novel, highly potent and selective OX2R agonist being developed for the treatment of select neurological and neurodegenerative disorders. ORX142 is the second drug candidate from the Company’s multi-asset orexin franchise. The Phase 1 study will evaluate the safety, tolerability and pharmacokinetics of single-ascending doses (SAD) and multiple-ascending doses (MAD) of ORX142 in healthy volunteers. In parallel to the SAD, a placebo-controlled crossover pharmacodynamic (PD) assessment will be performed utilizing the Maintenance of Wakefulness Test (MWT) and Karolinska Sleepiness Scale (KSS) in acutely sleep-deprived healthy adult subjects. The Company plans to initiate the first-in-human Phase 1 clinical study imminently, with clinical data expected 2025.Recent Insider Transactions Derivative • May 21CEO & Director exercised options and sold US$487k worth of stockOn the 20th of May, Saurabh Saha exercised 55k options at a strike price of around US$3.85 and sold these shares for an average price of US$12.71 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 12% salary and 88% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since June 2024, Saurabh's direct individual holding has decreased from 417.17k shares to 45.17k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.Recent Insider Transactions • Apr 24CEO & Director recently sold US$682k worth of stockOn the 22nd of April, Saurabh Saha sold around 55k shares on-market at roughly US$12.39 per share. This transaction amounted to 55% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger sale worth US$918k. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$6.1m.お知らせ • Apr 23Centessa Pharmaceuticals plc, Annual General Meeting, Jun 20, 2025Centessa Pharmaceuticals plc, Annual General Meeting, Jun 20, 2025. Location: offices of goodwin procter (uk) llp at sancroft, 10-15 newgate street, london, ec1a 7az, United KingdomPrice Target Changed • Mar 31Price target increased by 9.4% to US$31.25Up from US$28.57, the current price target is an average from 8 analysts. New target price is 117% above last closing price of US$14.38. Stock is up 30% over the past year. The company is forecast to post a net loss per share of US$1.53 next year compared to a net loss per share of US$2.06 last year.New Risk • Mar 24New major risk - Revenue sizeThe company makes less than US$1m in revenue. This is considered a major risk. Companies with a small amount of revenue are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Shareholders have been substantially diluted in the past year (35% increase in shares outstanding). Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$260m net loss in 3 years). Significant insider selling over the past 3 months (US$3.0m sold).Recent Insider Transactions • Mar 23CEO & Director recently sold US$918k worth of stockOn the 20th of March, Saurabh Saha sold around 55k shares on-market at roughly US$16.69 per share. This transaction amounted to 35% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$5.4m.Price Target Changed • Mar 14Price target increased by 9.3% to US$30.29Up from US$27.71, the current price target is an average from 7 analysts. New target price is 77% above last closing price of US$17.14. Stock is up 59% over the past year. The company is forecast to post a net loss per share of US$1.62 next year compared to a net loss per share of US$1.57 last year.Buy Or Sell Opportunity • Mar 07Now 22% undervalued after recent price dropOver the last 90 days, the stock has fallen 13% to US$16.23. The fair value is estimated to be US$20.80, however this is not to be taken as a buy recommendation but rather should be used as a guide only. Revenue has grown by 129% over the last 3 years. Earnings per share has grown by 36%. For the next 3 years, revenue is forecast to grow by 71% per annum. Earnings are also forecast to grow by 13% per annum over the same time period.Recent Insider Transactions • Feb 23CEO & Director recently sold US$876k worth of stockOn the 20th of February, Saurabh Saha sold around 55k shares on-market at roughly US$15.93 per share. This transaction amounted to 26% of their direct individual holding at the time of the trade. In the last 3 months, there was an even bigger sale from another insider worth US$1.2m. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$4.5m.Recent Insider Transactions Derivative • Feb 09Chief People Officer notifies of intention to sell stockKaren Anderson intends to sell 31k shares in the next 90 days after lodging an Intent To Sell Form on the 7th of February. If the sale is conducted around the recent share price of US$19.03, it would amount to US$581k. Since March 2024, Karen's direct individual holding has decreased from 77.69k shares to 54.32k. Company insiders have collectively sold US$10m more than they bought, via options and on-market transactions in the last 12 months.Recent Insider Transactions • Jan 23CEO & Director recently sold US$867k worth of stockOn the 21st of January, Saurabh Saha sold around 55k shares on-market at roughly US$15.77 per share. This transaction amounted to 25% of their direct individual holding at the time of the trade. In the last 3 months, there was an even bigger sale from another insider worth US$1.2m. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$3.6m.New Risk • Jan 16New major risk - Shareholder dilutionThe company's shareholders have been substantially diluted in the past year. Increase in shares outstanding: 35% This is considered a major risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risk Shareholders have been substantially diluted in the past year (35% increase in shares outstanding). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$240m net loss in 3 years). Significant insider selling over the past 3 months (US$4.3m sold).Buy Or Sell Opportunity • Jan 10Now 21% undervalued after recent price dropOver the last 90 days, the stock has fallen 2.2% to US$15.64. The fair value is estimated to be US$19.80, however this is not to be taken as a buy recommendation but rather should be used as a guide only. Revenue has grown by 129% over the last 3 years. Earnings per share has grown by 36%. For the next 3 years, revenue is forecast to grow by 71% per annum. Earnings are also forecast to grow by 14% per annum over the same time period.お知らせ • Jan 08Centessa Pharmaceuticals Announces Appointment of Stephen Kanes as Chief Medical OfficerCentessa Pharmaceuticals plc announced the appointment of Stephen Kanes MD PhD, as Chief Medical Officer (CMO). Dr. Kanes is a neuropsychiatrist, with a career in neuroscience, clinical psychiatry, and neuroscience drug development spanning more than 30 years. Dr. Kanes served as Chief Medical Officer of Sage Therapeutics from 2013 to 2021, where he led the successful clinical development of ZULRESSO® (brexanolone), the first-ever treatment approved for Postpartum Depression (PPD), along with the buildout of the development organization and Sage Therapeutics' broad neuroscience portfolio. Most recently, Dr. Kanes was Chief Executive Officer of EmbarkNeuro, a neuroscience focused biotech company. Earlier in his career, Dr. Kanes was Executive Director in Clinical Development in the Inflammation, Neuroscience and Respiratory therapeutic areas at AstraZeneca, and a faculty member of the University of Pennsylvania Department of Psychiatry where he explored both the genetics and physiology of severe mental illness. He has authored or co-authored more than 60 peer-reviewed publications in behavioral neuroscience, behavioral pharmacology, genetics, brain imaging, clinical trials, and health economics and serves as an ad hoc reviewer for multiple journals including Neuropsychopharmacology andThe American Journal of Medical Genetics and Biological Psychiatry. Dr. Kanes received his BA from the University of Pennsylvania in the Biological Basis of Behavior and both his PhD in Molecular and Cellular Pharmacology and MD from the Stony Brook University Renaissance School of Medicine. He completed his psychiatry residency at Yale-New Haven Medical Center and a neuropsychiatry postdoctoral fellowship at the University of Pennsylvania.Seeking Alpha • Dec 31Centessa Pharmaceuticals: Orexin Franchise Worth MonitoringSummary Centessa Pharmaceuticals, founded from the merger of 10 biotech companies, is based on an asset-centric model, primarily developing its lead orexin agonist, ORX-750. ORX-750 targets narcolepsy types 1 and 2 and idiopathic hypersomnia, showing promising phase 1 results, with phase 2 data expected in 2025. Takeda's TAK-861 success partially de-risks ORX-750, making Centessa a potential acquisition target if ORX-750 proves it is best-in-class. With $500M in cash and a runway into mid-2027, Centessa's phase 2 trial results for ORX-750 are crucial for its future valuation. Read the full article on Seeking AlphaRecent Insider Transactions • Dec 19General Counsel recently sold US$1.2m worth of stockOn the 16th of December, Iqbal Hussain sold around 72k shares on-market at roughly US$16.39 per share. This transaction amounted to 76% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Insiders have been net sellers, collectively disposing of US$3.6m more than they bought in the last 12 months.Recent Insider Transactions Derivative • Dec 09CEO & Director exercised options and sold US$1.1m worth of stockOn the 6th of December, Saurabh Saha exercised 87k options at a strike price of around US$5.84 and sold these shares for an average price of US$18.46 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since December 2023, Saurabh's direct individual holding has increased from 313.17k shares to 526.82k. Company insiders have collectively sold US$6.0m more than they bought, via options and on-market transactions in the last 12 months.Recent Insider Transactions • Nov 25CEO & Director recently sold US$929k worth of stockOn the 20th of November, Saurabh Saha sold around 55k shares on-market at roughly US$16.89 per share. This transaction amounted to 19% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$1.8m.New Risk • Nov 20New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 2.1% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risk Earnings are forecast to decline by an average of 2.1% per year for the foreseeable future. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$237m net loss in 3 years). Shareholders have been diluted in the past year (35% increase in shares outstanding). Significant insider selling over the past 3 months (US$1.3m sold).Price Target Changed • Nov 17Price target increased by 8.2% to US$28.29Up from US$26.14, the current price target is an average from 7 analysts. New target price is 77% above last closing price of US$16.00. Stock is up 127% over the past year. The company is forecast to post a net loss per share of US$1.66 next year compared to a net loss per share of US$1.57 last year.お知らせ • Nov 13Centessa Pharmaceuticals Initiates Phase 2 Trial with ORX750, a Novel Orexin Receptor 2 (OX2R) AgonistNxera Pharma Co. Ltd. announced that Centessa Pharmaceuticals has initiated a Phase 2 trial of ORX750, an investigational, orally administered, highly potent and selective orexin receptor 2 (OX2R) antagonist for the treatment of narcolepsy type 1 (NT1), narcolepsy type 2 (NT2), and idiopathic hypersomnia. The achievement of this milestone results in a payment of USD 3.5 million to Nxera pursuant to its research collaboration with Centessa. This will be recognised as revenue in Fourth Quarter Fiscal Year 2024. ORX750 was designed using Nxera technology to directly target the underlying pathophysiology of orexin neuron loss in NT1, with potential applicability to NT2, idiopathic hypersomnia, and other sleep- wake disorders with normal orexin levels.Recent Insider Transactions • Oct 25CEO & Director recently sold US$864k worth of stockOn the 23rd of October, Saurabh Saha sold around 55k shares on-market at roughly US$15.70 per share. This transaction amounted to 16% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. This was Saurabh's only on-market trade for the last 12 months.Recent Insider Transactions Derivative • Oct 24CEO & Director notifies of intention to sell stockSaurabh Saha intends to sell 22k shares in the next 90 days after lodging an Intent To Sell Form on the 21st of October. If the sale is conducted around the recent share price of US$15.80, it would amount to US$351k. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since December 2023, Saurabh's direct individual holding has increased from 313.17k shares to 708.09k. Company insiders have collectively sold US$2.7m more than they bought, via options and on-market transactions in the last 12 months.Recent Insider Transactions • Sep 29Chief Business Officer recently sold US$261k worth of stockOn the 25th of September, Gregory Weinhoff sold around 17k shares on-market at roughly US$15.69 per share. This transaction amounted to 19% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. This was the only on-market transaction from insiders over the last 12 months.Seeking Alpha • Sep 25Centessa Pharmaceuticals: Progressing SerpinPC Through Registrational Trials In Hemophilia BSummary Centessa Pharma's SerpinPC, a subcutaneous biologic inhibitor, shows promising results in reducing bleeding rates in hemophilia B, with a favorable safety profile. Despite the stock doubling in value, I remain cautious due to the company's unclear business strategy and lack of registrational data. The hemophilia B market is competitive with existing treatments. SerpinPC's unique mechanism and delivery method provide niche advantages but face significant competition. With a $2bn market cap and a cash runway of 6-7 quarters, I will avoid investing until there's more clarity on their strategic direction. Read the full article on Seeking AlphaRecent Insider Transactions Derivative • Sep 23CEO & Director notifies of intention to sell stockSaurabh Saha intends to sell 55k shares in the next 90 days after lodging an Intent To Sell Form on the 20th of September. If the sale is conducted around the recent share price of US$16.45, it would amount to US$905k. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since September 2023, Saurabh's direct individual holding has increased from 274.44k shares to 724.35k. Company insiders have collectively sold US$2.4m more than they bought, via options and on-market transactions in the last 12 months.お知らせ • Sep 12Centessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $150 million.Centessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $150 million. Security Name: American Depositary Shares Security Type: Depositary Receipt (Common Stock)Recent Insider Transactions Derivative • Sep 11Chief Business Officer notifies of intention to sell stockGregory Weinhoff intends to sell 25k shares in the next 90 days after lodging an Intent To Sell Form on the 9th of September. If the sale is conducted around the recent share price of US$15.00, it would amount to US$375k. Since September 2023, Gregory's direct individual holding has increased from 76.64k shares to 206.44k. There have been no trades via on-market transactions or options from company insiders in the last 12 months.Price Target Changed • Sep 10Price target increased by 10% to US$16.00Up from US$14.50, the current price target is an average from 6 analysts. New target price is 9.7% above last closing price of US$14.58. Stock is up 117% over the past year. The company is forecast to post a net loss per share of US$1.61 next year compared to a net loss per share of US$1.57 last year.お知らせ • Sep 10Centessa Pharmaceuticals plc Announces Positive Interim Phase 1 Clinical Data with Its Novel Orexin Receptor 2 (OX2R) Agonist, Orx750, in Acutely Sleep-Deprived Healthy VolunteersCentessa Pharmaceuticals plc announced positive interim data from an ongoing Phase 1 trial of its highly potent and selective orexin receptor 2 (OX2R) agonist, ORX750, in acutely sleep-deprived healthy volunteers. ORX750 showed clinically meaningful and statistically significant improvements in mean sleep latency at the first two doses evaluated (1.0 mg and 2.5 mg) in the Maintenance of Wakefulness Test (MWT) compared to placebo. More specifically, the 2.5 mg dose was shown to restore normative wakefulness2 with a mean sleep latency of 32 minutes as measured by the MWT. ORX750 was also shown to have a favorable safety and tolerability profile with no observations of frequently reported on-target adverse events (AEs) associated with other OX2R agonists, and no cases of hepatotoxicity or visual disturbances across all three dose levels tested (1.0 mg, 2.0 mg, and 2.5 mg), as of the data cutoff date.1 Based on the interim data, the Company plans to rapidly advance ORX750 into Phase 2 studies in patients with narcolepsy type 1 (NT1), narcolepsy type 2 (NT2), and idiopathic hypersomnia (IH) beginning in the fourth quarter of 2024. The Phase 1 clinical study is an ongoing first-in-human, randomized, placebo-controlled study designed to evaluate the safety, tolerability and pharmacokinetics (PK) of single-ascending doses (SAD) and multiple-ascending doses (MAD) of ORX750 in healthy adult subjects. In parallel to the SAD, a placebo-controlled cross-over pharmacodynamic (PD) assessment is being performed utilizing the MWT and Karolinska Sleepiness Scale (KSS) in acutely sleep-deprived healthy adult subjects with the goal of rapidly generating early efficacy data to inform dosing for planned studies in patients. As of September 10, 2024, the study has completed three SAD cohorts of healthy volunteers (27 active, 9 placebo) with doses of 1.0 mg, 2.0 mg, and 2.5 mg, and has advanced through two cohorts within the cross-over assessment of acutely sleep-deprived healthy volunteers with doses of 1.0 mg (n=8) and 2.5 mg (n=8), administered as a single oral dose. Dosing in the MAD portion of the study is also ongoing.Recent Insider Transactions Derivative • Aug 26CEO & Director notifies of intention to sell stockSaurabh Saha intends to sell 47k shares in the next 90 days after lodging an Intent To Sell Form on the 23rd of August. If the sale is conducted around the recent share price of US$12.30, it would amount to US$574k. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since September 2023, Saurabh's direct individual holding has increased from 274.44k shares to 333.83k. There have been no trades via on-market transactions or options from company insiders in the last 12 months.Price Target Changed • Jun 21Price target increased by 9.2% to US$14.20Up from US$13.00, the current price target is an average from 5 analysts. New target price is 60% above last closing price of US$8.86. Stock is up 34% over the past year. The company is forecast to post a net loss per share of US$1.63 next year compared to a net loss per share of US$1.57 last year.お知らせ • Jun 13+ 1 more updateCentessa Pharmaceuticals plc Announces Chief Financial Officer ChangesOn June 10, 2024, Centessa Pharmaceuticals plc (the Company) announced the appointment of John Crowley as Chief Financial Officer, which was approved by the Board of Directors of the Company on June 5, 2024, effective June 10, 2024 (the Start Date). Accordingly, Mr. Crowley has also been designated the Company’s principal financial officer and principal accounting officer, replacing Dr. Gregory Weinhoff as Chief Financial Officer and in those roles. John Crowley CPA, Chief Financial Officer: Mr. Crowley brings over 20 years of global finance and operational experience in the life sciences industry to Centessa. He most recently served as Chief Financial Officer of Fusion Pharmaceuticals prior to its acquisition by AstraZeneca in June 2024. He also served as Executive Vice President and Chief Financial Officer of Merus Inc. Prior to Merus, Mr. Crowley served as the Corporate Senior Vice President, Corporate Controller and Chief Accounting Officer of Charles River Laboratories Inc. Previously, Mr. Crowley held senior corporate finance positions at Ironwood Pharmaceuticals Inc., Vertex Pharmaceuticals Inc., and Sunovion Pharmaceuticals Inc., where he supported several commercial launches, financings, and business development transactions in rapidly growing companies. Mr. Crowley is a Certified Public Accountant and graduated Summa Cum Laude from Babson College with BS degrees in both Economics and Accountancy. Dr. Weinhoff served as Chief Financial Officer of Centessa from March 2021 to June 2024. He brings over 20 years of business development experience to the newly created position of Chief Business Officer. Prior to Centessa, Dr. Weinhoff was co-founder, director and chief financial and business officer of Arvelle Therapeutics B.V., which was acquired by Angelini Pharma in 2021. While with Arvelle, he led the asset identification and in-licensing of cenobamate, a novel anti-seizure medicine. Prior to Arvelle, Dr. Weinhoff served as Chief Financial Officer at Axovant Sciences Inc., where he led financial functions and the execution of several private and public financings. Before Axovant, Dr. Weinhoff spent 15 years as an early-stage healthcare venture capitalist at CHL Medical Partners, where he was founding CEO of Amicus Therapeutics and his firm was the sole Series A investor. Dr. Weinhoff holds an MD from Harvard Medical School, an MBA from Harvard Business School and an AB in economics from Harvard College. Prior to graduate school, Dr. Weinhoff was a financial analyst in Morgan Stanley & Co.’s healthcare corporate finance group.Board Change • Jun 02Insufficient new directorsThere is 1 new director who has joined the board in the last 3 years. The company's board is composed of: 1 new director. 7 experienced directors. No highly experienced directors. Independent Non-Executive Director Mathias Hukkelhoven was the last director to join the board, commencing their role in 2022. The company’s insufficient board refreshment is considered a risk according to the Simply Wall St Risk Model.お知らせ • Apr 25+ 1 more updateCentessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $100 million.Centessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $100 million. Security Name: American Depositary Shares Security Type: Depositary Receipt (Common Stock)Seeking Alpha • Apr 24Centessa: Hemophilia B Data Readout In 2024 Is Major Turning PointSummary Centessa Pharmaceuticals plc interim data from the PRESent-2 study, using SerpinPC for the treatment of patients with Hemophilia B without inhibitors, is expected to be released in 2024. PRESent-3 is another registrational study using SerpinPC for the treatment of patients with Hemophilia B, however it is for the targeting of such patients with inhibitors. ORX750 is an oral selective orexin receptor agonist being developed for the treatment of patients with Narcolepsy Type 1; Proof of concept data to be released in second half 2024. LB101 is another product in the pipeline with great potential targeting solid tumors, because it utilizes proven targeted proteins such as PD-L1 and CD47; The PD-L1 blockade occurs first as a block mechanism then with hinges dissolving moves the CD47 into place to perform mechanism of action. Read the full article on Seeking Alphaお知らせ • Apr 23Centessa Pharmaceuticals plc Announces Open IND for ORX750Centessa Pharmaceuticals plc announced that the U.S. Food and Drug Administration (FDA) has cleared the Investigational New Drug application (IND) to initiate a Phase 1 first-in-human, clinical trial of ORX750 for the treatment of narcolepsy. ORX750 is an investigational, orally administered, highly potent and selective orexin receptor 2 (OX2R) agonist designed to directly target the underlying pathophysiology of orexin neuron loss in narcolepsy type 1 (NT1), with potential applicability to narcolepsy type 2 (NT2), idiopathic hypersomnia (IH), and other sleep-wake disorders with normal orexin levels. The Phase 1 study will evaluate the safety, tolerability and pharmacokinetics of single-ascending doses (SAD) and multiple-ascending doses (MAD) of ORX750 in healthy adult subjects. In parallel to the SAD, a cross-over pharmacodynamic (PD) assessment will be performed utilizing the Maintenance of Wakefulness Test (MWT) and Karolinska Sleepiness Scale (KSS) in acutely sleep-deprived healthy adult subjects which is intended to provide proof-of-concept data to enable dose selection for NT1, NT2 and IH indications. The study has a maximum exposure limit specified by the FDA which the Company believes significantly exceeds the predicted efficacious doses of ORX750 in indications associated with or without orexin loss; therefore, the Company does not expect this limit to affect any of the planned clinical development activities for ORX750. The Company expects to commence dosing of the Phase 1 study in healthy volunteers imminently, and proof-of-concept data are anticipated in the second half of 2024. ORX750 is an investigational, orally administered, highly potent and selective orexin receptor 2 (OX2R) agonist designed to directly target the underlying pathophysiology of orexin neuron loss in narcolepsy type 1 (NT1). ORX750 has been shown to potently activate the OX2R with an in vitro EC50 of 0.11 nM and 9,800-fold selectivity over the human orexin receptor (hOX1R). ORX750 is Centessa’s first orexin product candidate being developed for the treatment of narcolepsy with potential expansion into narcolepsy type 2 (NT2), idiopathic hypersomnia (IH) and other sleep-wake disorders.New Risk • Mar 05New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 0.3% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 0.3% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$218m net loss in 3 years). Share price has been volatile over the past 3 months (12% average weekly change). Shareholders have been diluted in the past year (3.2% increase in shares outstanding).お知らせ • Dec 11Centessa Pharmaceuticals plc Announces New Data from an Additional 52-Weeks of Continuous Treatment from Third Year (Part 5) of Ongoing Phase 2A Study of Serpinpc for the Treatment of HemophiliaCentessa Pharmaceuticals plc announced new data from an additional 52-we weeks of continuous treatment from the third year (Part 5) of the ongoing Phase 2a study of SerpinPC for the treatment of hemophilia. The data were shared in a poster presentation at the American Society of Hematology (ASH) Annual Meeting on December 10, 2023. During treatment with SerpinPC all breakthrough bleeds were treated on-demand w ith usual clotting factor concentrate, without dose reduction and without limitation of number of infusions. Data from Part 5 were presented at the ASH Annual Meeting in a poster titled: SerpinPC in persons with severe hemophilia (PwH): Updated results from a multi-center, multi-part, first-in-human study.お知らせ • Nov 01Centessa Pharmaceuticals plc Announces Dosing of First Subject in Registrational Present-3 Study Evaluating Serpinpc for the Treatment of Hemophilia B with InhibitorsCentessa Pharmaceuticals plc announced the dosing of the first subject in its registrational Present-3 study of SerpinPC for the treatment of hemophilia B with inhibitors. The dosing phase of Present-3 follows a minimum 12-week observation period during which prospective baseline data of the subject's disease status under their current therapy are collected to support regulatory review of the benefit and risk profile of SerpinPC. SerpinPC is a subcutaneously administered novel inhibitor of APC being developed as a potential treatment for hemophilia, regardless of severity or inhibitor status, and which may also be developed to prevent bleeding associated with other bleeding disorders. The registrational program for SerpinPC in hemophilia B includes a set of clinical studies with multiple components. Present-5 is an observational feeder study to collect prospective observational data for minimum defined periods before switching to dosing subjects in the interventional studies. The U.S. Food and Drug Administration (FDA) has granted Fast Track designation to SerpinPC for the treatmentof hemophilia B, with or without inhibitors. SerpinPC is an investigational agent that has not been approved by the FDA or any other regulatory authority.お知らせ • Oct 26Centessa Pharmaceuticals plc Announces Preclinical Data Supporting Orx750's Potential as A Best-In-Class Oral Ox2r Agonist for the Treatment of Narcolepsy and Other Sleep-Wake DisordersCentessa Pharmaceuticals plc announced a robust set of new preclinical data from in vivo and in vitro studies of its investigational, novel orexin receptor 2 (OX2R) agonist, ORX750, that support its potential best-in-class profile for the treatment of narcolepsy and other sleep- wake disorders. ORX750 is an investigational, orally administered, highly potent and selective orexin receptor 2 (ox2R) agonist designed to directly target the underlying pathophysiology of orexin neuron loss in narcolepsy type 1 (NT1). ORX750 is Centessa's first orexin product candidate being developed for the treatment of narcolpsy with potential expansion into other sleep- wake disorders.ORX750 is currently undergoing IND-enabling activities and has not been administered as an investigational drug to humans in any jurisdiction. Any such statements that are not statements of historical fact may be deemed to be forward-looking statements, including statements related to: the Company's ability to deliver transformational medicines to patients; the activity significance of low doses in highly predictive, translational models of narcolepsy type 1 ("NT1") including maximal wake times and suppressed cataplexy at the lowest oral dose tested; the Company's expectations on the timing of Ind-enabling studies of ORX750 in narcolepsy and other Sleep- wake disorders; the ability of management team and board to drive execution of the Company's portfolio of programs; asset-centric business model and the intended advantages and benefits thereof; the scope, progress, results and costs of developing product candidates or any other future product candidates; current expectations concerning, amongst other things, the development and therapeutic potential and benefits of product candidates, including ORX750 and other OX2R agonists; strategy; regulatory matters, including the timing and likelihood of initiating clinical trials, reporting clinical trial results, ability to initiate or continue clinical trials or market any products; and the market size and opportunity for product candidates. Based on current expectations, estimates and projections only as of the date of this release and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set out in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, risks related to the safety and tolerability profile of product candidates including ORX750; ability to protect and maintain intellectual property position; business (including commercial viability), regulatory, economic and competitive risks, uncertainties, contingencies and assumptions about the Company; risks inherent in developing product candidates and technologies; ability to obtain adequate financing, including through financing facility with Oberland, to fund planned clinical trials and other expenses; trends in the industry; the legal and regulatory framework for the industry, including the receipt and maintenance of clearances to conduct or continue clinical testing; future expenditures risks related to asset-centric corporate model; the risk that any one or more of product candidates will not be successfully developed and/or commercialized; and the risk that the results of non-clinical studies or clinical studies will not be predictive of future results.Recent Insider Transactions Derivative • Sep 22Insider notifies of intention to sell stockHarris Rotman intends to sell 37k shares in the next 90 days after lodging an Intent To Sell Form on the 20th of September. If the sale is conducted around the recent share price of US$6.50, it would amount to US$244k. Since June 2023, Harris has owned 33.50k shares directly. There have been no trades via on-market transactions or options from company insiders in the last 12 months.お知らせ • Aug 25World Sleep Congress Releases an Abstract Submit by Centessa Pharmaceuticals plcOn August 22, 2023, the World Sleep Congress 2023 released an abstract submitted by Centessa Pharmaceuticals Plc. containing preclinical data on ORX750, the company's orally administered, selective orexin receptor 2 (OX2R) agonist in development for the treatment of narcolepsy and other sleep disorders. The company will present the abstract in an oral presentation on October 25, 2023. Introduction: Narcolepsy Type 1 (NT1) is a rare neurological disease caused by the profound loss of orexin-producing neurons. Orexin (also called hypocretin) is a neurotransmitter that regulates wakefulness, arousal, and energy homeostasis via activation of Orexin Receptor-1 (OX1R) and -2 (OX2R). Orexin agonists are designed to directly address the underlying disease pathology of NT1 to restore orexin neurotransmission in the brain. The orexin/ataxin-3 (Atax) mouse model of NT1 recapitulates key features of the human disorder, such as orexin loss, inability to sustain wakefulness, and cataplexy (emotionally triggered, transient loss of muscle tone). Here it present ORX750, a novel, orally available, brain penetrant, OX2R selective agonist. ORX750 was developed using structure-based drug design with an OX2R stabilized receptor (StaR®) protein and high-resolution protein crystallography. Materials and Methods: In vitro calcium mobilization (FLIPR), ß-arrestin recruitment, and inositol-phosphate accumulation assays were performed in Chinese hamster ovary (CHO) cells stably expressing human recombinant OX1R or OX2R. Electrophysiological recordings were performed on slices of the ventral tuberomammillary nucleus (TMN) from mouse hypothalamus; effects on membrane potential were measured in the presence of 1 micromolar tetrodotoxin to block neuron firing. In vivo efficacy for enhancing wakefulness was evaluated in wild type (WT) and Atax mice during their rest phase using PiezoSleep, a rapid, non-invasive method for classifying sleep and wakefulness by unsupervised machine learning on physiologically relevant readouts, including body movement and breath rate. Electroencephalogram (EEG), electromyogram (EMG), and video recordings were used in Atax mice during their active phase to evaluate effects at 0.3-10 mg/kg on arousal states and cataplexy. Results: ORX750 behaved as a potent full agonist at human OX2R (EC50=0.11 nM) relative to the native ligand orexin A (OXA; EC50=0.035 nM) and showed 9,800-fold selectivity over human OX1R (EC50=1100 nM) in the FLIPR assay. Biased agonism was not detected by measurement of b-arrestin recruitment at OX2R in comparison to OXA. ORX750 depolarized membrane potential (EC50=5.0 nM, max DmV=9.5) in whole cell current-clamp recordings in the TMN. In the PiezoSleep assay, in which wakefulness readouts are highly correlated with EEG/EMG-defined wakefulness, ORX750 increased time awake and the consolidation of wakefulness vs. vehicle in a dose-related manner when administered to WT and Atax mice during the rest phase. Increased sensitivity to these wake-promoting effects was observed in Atax vs. WT mice. In Atax mice, ORX750 increased time awake; consolidated wakefulness; increased EEG gamma power during wakefulness; reduced cataplexy occurrences; and increased latencies to sleep and cataplexy in a dose-related manner during the active phase using the EEG/EMG/video assay. At the lowest dose tested (0.3 mg/kg) and compared to vehicle, the latency to sleep was 2.3 h vs. 0.69 h and the latency to cataplexy was 2.7 h vs. 1.3 h. Conclusions: ORX750 is an oral, highly potent, and selective OX2R agonist with the potential to treat patients with primary symptoms of NT1, as well as reduce excessive sleepiness in those presenting sleep/wake disorders with normal orexin levels.New Risk • Aug 14New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 0.5% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 0.5% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$233m net loss in 3 years). Share price has been volatile over the past 3 months (14% average weekly change).Price Target Changed • Jul 25Price target increased by 18% to US$7.08Up from US$6.00, the current price target is an average from 6 analysts. New target price is approximately in line with last closing price of US$7.14. Stock is up 62% over the past year. The company is forecast to post a net loss per share of US$1.99 next year compared to a net loss per share of US$2.31 last year.お知らせ • Jul 12Centessa Pharmaceuticals Announces Dosing of First Subject in Registrational PRESent-2 Study Evaluating SerpinPC for the Treatment of Hemophilia B Without InhibitorsCentessa Pharmaceuticals plc announced the dosing of the first subject in its registrational PRESent-2 study of SerpinPC for the treatment of hemophilia B without inhibitors. The dosing phase of PRESent-2 follows a minimum 12-week observation period during which prospective baseline data of the subject’s disease status under their current therapy are collected to support regulatory review of the benefit and risk profile of SerpinPC. SerpinPC is an investigational subcutaneously administered novel inhibitor of activated protein C (APC) being developed as a potential treatment for hemophilia B, with or without inhibitors. The PRESent-2 study (AP-0102) is a Phase 2b, global, open-label, seamless adaptive design study to investigate the efficacy and safety of subcutaneous dosing of SerpinPC every week, every 2 weeks, or every 4 weeks in approximately 120 adult (aged 18 to =65 years) or adolescent (aged =12 to <18 years) male subjects with severe hemophilia A (with or without inhibitors) or moderately severe to severe hemophilia B (without inhibitors). PRESent-2 consists of 3 parts: a 24-week randomized dose-justification phase (Part 1), a 24-week dose-confirmatory phase (Part 2), and a further 24-week extension phase (Part 3) for subjects who complete either Part 1 or Part 2. Subjects must have undergone a minimum period of prospective observation (at least 12 weeks for Part 1 or 24 weeks for Part 2) under their current therapy (either on-demand or prophylaxis factor replacement) before switching to SerpinPC treatment. The primary efficacy endpoint for the study is the rate of treated bleeds (expressed as an annualized bleeding rate (ABR)) in the observation period compared to the first 24 weeks treated with SerpinPC. The Company expects to begin dosing in its registrational PRESent-3 (AP-0103) study for subjects with hemophilia B with inhibitors this year.New Risk • Jul 06New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of American stocks, typically moving 10% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$235m net loss in 3 years). Share price has been volatile over the past 3 months (10% average weekly change).お知らせ • May 23Centessa Pharmaceuticals Receives Fast Track Designation from the U.S. FDA for Serpinpc for Hemophilia BCentessa Pharmaceuticals plc announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to SerpinPC, an investigational novel inhibitor of activated protein C (APC) being developed for the treatment of hemophilia B, with or without inhibitors. According to the FDA, Fast Track is a process designed to facilitate the development and expedite the review of drug candidates to treat serious conditions and fulfill an unmet medical need. A therapeutic candidate that receives Fast Track designation may be eligible for more frequent interactions with the FDA to discuss the candidate’s development plan and, if relevant criteria are met, eligibility for Accelerated Approval, Priority Review, or Rolling Review.お知らせ • Jan 27Centessa Pharmaceuticals Announces FDA Clearance of IND Application for Phase 1/2a Clinical Trial of LB101, First LockBody® Candidate, for Solid TumorsCentessa Pharmaceuticals plc announced that it has received clearance of its Investigational New Drug (IND) application from the U.S. Food and Drug Administration (FDA) to initiate a Phase 1/2a first-in-human, clinical trial of LB101 for the treatment of solid tumors. LB101, a conditionally tetravalent PD-L1xCD47 LockBody® bispecific monoclonal antibody targeting solid tumors, is the first product candidate developed using the Company’s proprietary LockBody technology which is designed to selectively drive potent effector function activity, such as CD47, in the tumor microenvironment (TME) while avoiding systemic toxicity.Price Target Changed • Nov 16Price target decreased to US$6.00Down from US$9.50, the current price target is an average from 4 analysts. New target price is 70% above last closing price of US$3.53. Stock is down 72% over the past year. The company posted a net loss per share of US$5.07 last year.Board Change • Nov 16High number of new and inexperienced directorsThere are 8 new directors who have joined the board in the last 3 years. The company's board is composed of: 8 new directors. No experienced directors. No highly experienced directors. Independent Chairman of the Board Francesco de Rubertis is the most experienced director on the board, commencing their role in 2020. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.Seeking Alpha • Oct 20Centessa Pharmaceuticals snaps multi-day losing streak; up 10%For the first time since Oct. 13, Centessa Pharmaceuticals (NASDAQ:CNTA) is showing gains. In Thursday afternoon trading, the biotech is up 10%. There is no news or other catalysts that might explain the jump. However, based on a technical analysis, Centessa (CNTA) deviated two standard deviations lower from its mean touching its lower Bolinger Band level and has snapped up higher, back to its mean level. From market close Oct. 13 through market close Oct. 19, shares fell ~15%. Seeking Alpha views Centessa (CNTA) as a hold with high marks for valuation and growth.Seeking Alpha • Sep 14Centessa hemophilia B therapy SerpinPC gets FDA orphan drug statusThe U.S. Food and Drug Administration (FDA) granted orphan drug designation to Centessa Pharmaceuticals' (NASDAQ:CNTA) SerpinPC to treat hemophilia B. The U.K.-based company said in a Sept. 14 press release that it plans to begin registrational studies of SerpinPC in Q4 2022. SerpinPC is a biological drug candidate, based on the serpin family of proteins which is designed to allow more thrombin to be generated by inhibiting activated protein C (APC), thus rebalancing coagulation in patients with hemophilia, according to Centessa. "We believe SerpinPC has the potential to offer patients with hemophilia B a convenient subcutaneous option that is designed to prevent and reduce bleeds without the risk of thrombosis," said Centessa CEO Saurabh Saha. The FDA grants orphan drug status to therapies which treat or prevent rare diseases that affect fewer than 200K people in the U.S. The designation provides certain incentives, including up to seven years of market exclusivity, if approved.Seeking Alpha • Aug 10Centessa Pharmaceuticals GAAP EPS of -$0.69Centessa Pharmaceuticals press release (NASDAQ:CNTA): Q2 GAAP EPS of -$0.69. Cash and Cash Equivalents: $484.2 million as of June 30, 2022, which the Company expects will fund operations into 2026, without drawing on the remaining available tranches under the Oberland credit facility.Board Change • Apr 27High number of new and inexperienced directorsThere are 8 new directors who have joined the board in the last 3 years. The company's board is composed of: 8 new directors. No experienced directors. No highly experienced directors. Independent Chairman of the Board Francesco de Rubertis is the most experienced director on the board, commencing their role in 2020. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.Board Change • Apr 05High number of new and inexperienced directorsThere are 8 new directors who have joined the board in the last 3 years. The company's board is composed of: 8 new directors. No experienced directors. No highly experienced directors. Independent Chairman of the Board Francesco de Rubertis is the most experienced director on the board, commencing their role in 2020. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.Seeking Alpha • Dec 23Checking In On Centessa PharmaceuticalsToday, we put Centessa Pharmaceuticals in the spotlight for the first time. Centessa has a unique business model, multiple potential shots on goal, is deep in Busted IPO territory and has picked up some recent insider buying. A full investment analysis follows in the paragraphs below.収支内訳Centessa Pharmaceuticals の稼ぎ方とお金の使い方。LTMベースの直近の報告された収益に基づく。収益と収入の歴史NasdaqGS:CNTA 収益、費用、利益 ( )USD Millions日付収益収益G+A経費研究開発費31 Mar 260-2515819931 Dec 2515-1985017230 Sep 2515-2435017930 Jun 2515-2305017131 Mar 2515-2245016131 Dec 240-2365115030 Sep 247-1614911930 Jun 247-1574911331 Mar 247-1385111431 Dec 237-1515412430 Sep 230-1575512330 Jun 230-1735513131 Mar 230-2125715131 Dec 220-2165515530 Sep 220-2345416930 Jun 220-2205515831 Mar 220-1975212231 Dec 210-381439630 Sep 210-324305730 Jun 210-286183431 Mar 210-24661731 Dec 200-1119質の高い収益: CNTAは現在利益が出ていません。利益率の向上: CNTAは現在利益が出ていません。フリー・キャッシュフローと収益の比較過去の収益成長分析収益動向: CNTAは利益を出していないが、過去 5 年間で年間6.7%の割合で損失を削減してきた。成長の加速: CNTAの過去 1 年間の収益成長を 5 年間の平均と比較することはできません。現在は利益が出ていないためです。収益対業界: CNTAは利益が出ていないため、過去 1 年間の収益成長をBiotechs業界 ( 43% ) と比較することは困難です。株主資本利益率高いROE: CNTAは現在利益が出ていないため、自己資本利益率 ( -51.43% ) はマイナスです。総資産利益率使用総資本利益率過去の好業績企業の発掘7D1Y7D1Y7D1YPharmaceuticals-biotech 、過去の業績が好調な企業。View Financial Health企業分析と財務データの現状データ最終更新日（UTC時間）企業分析2026/05/21 13:59終値2026/05/21 00:00収益2026/03/31年間収益2025/12/31データソース企業分析に使用したデータはS&P Global Market Intelligence LLC のものです。本レポートを作成するための分析モデルでは、以下のデータを使用しています。データは正規化されているため、ソースが利用可能になるまでに時間がかかる場合があります。パッケージデータタイムフレーム米国ソース例会社財務10年損益計算書キャッシュ・フロー計算書貸借対照表SECフォーム10-KSECフォーム10-Qアナリストのコンセンサス予想+プラス3年予想財務アナリストの目標株価アナリストリサーチレポートBlue Matrix市場価格30年株価配当、分割、措置ICEマーケットデータSECフォームS-1所有権10年トップ株主インサイダー取引SECフォーム4SECフォーム13Dマネジメント10年リーダーシップ・チーム取締役会SECフォーム10-KSECフォームDEF 14A主な進展10年会社からのお知らせSECフォーム8-K* 米国証券を対象とした例であり、非米国証券については、同等の規制書式および情報源を使用。特に断りのない限り、すべての財務データは1年ごとの期間に基づいていますが、四半期ごとに更新されます。これは、TTM（Trailing Twelve Month）またはLTM（Last Twelve Month）データとして知られています。詳細はこちら。分析モデルとスノーフレーク本レポートを生成するために使用した分析モデルの詳細は当社のGithubページでご覧いただけます。また、レポートの使用方法に関するガイドやYoutubeのチュートリアルも掲載しています。シンプリー・ウォールストリート分析モデルを設計・構築した世界トップクラスのチームについてご紹介します。業界およびセクターの指標私たちの業界とセクションの指標は、Simply Wall Stによって6時間ごとに計算されます。アナリスト筋Centessa Pharmaceuticals plc 12 これらのアナリストのうち、弊社レポートのインプットとして使用した売上高または利益の予想を提出したのは、 。アナリストの投稿は一日中更新されます。21 アナリスト機関Mayank MamtaniB. Riley Securities, Inc.Umer RaffatEvercore ISIAndrea NewkirkGoldman Sachs18 その他のアナリストを表示
New Risk • May 06New major risk - Revenue sizeThe company makes less than US$1m in revenue. This is considered a major risk. Companies with a small amount of revenue are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$145m net loss in 3 years). Share price has been volatile over the past 3 months (14% average weekly change). Shareholders have been diluted in the past year (16% increase in shares outstanding). Significant insider selling over the past 3 months (US$2.2m sold).
お知らせ • May 04Centessa Pharmaceuticals plc, Annual General Meeting, Jun 12, 2026Centessa Pharmaceuticals plc, Annual General Meeting, Jun 12, 2026. Location: sancroft, 10-15 newgate street, ec1a 7az, london United Kingdom
New Risk • Apr 02New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 16% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$216m net loss in 3 years). Share price has been volatile over the past 3 months (14% average weekly change). Shareholders have been diluted in the past year (16% increase in shares outstanding). Significant insider selling over the past 3 months (US$3.2m sold).
New Risk • Mar 31New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of American stocks, typically moving 6.5% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$203m net loss in 3 years). Share price has been volatile over the past 3 months (6.5% average weekly change). Significant insider selling over the past 3 months (US$3.2m sold).
Price Target Changed • Mar 31Price target increased by 8.0% to US$42.36Up from US$39.23, the current price target is an average from 10 analysts. New target price is 6.7% above last closing price of US$39.71. The company is forecast to post a net loss per share of US$1.38 next year compared to a net loss per share of US$2.06 last year.
お知らせ • Mar 31Eli Lilly and Company (NYSE:LLY) entered into a definitive agreement to acquire Centessa Pharmaceuticals plc (NasdaqGS:CNTA) from Medicxi Ventures (UK) LLP, Index Ventures SA, General Atlantic Service Company, L.P. and other shareholders for $5.6 billion.Eli Lilly and Company (NYSE:LLY) entered into a definitive agreement to acquire Centessa Pharmaceuticals plc (NasdaqGS:CNTA) from Medicxi Ventures (UK) LLP, Index Ventures SA, General Atlantic Service Company, L.P. and other shareholders for $5.6 billion on March 31, 2026. Under the terms of the transaction agreement, Eli Lilly will acquire all of the issued and to be issued share capital of Centessa (including the American Depositary Shares (ADSs) representing ordinary shares) for $38.00 in cash per share plus one non-transferrable contingent value right (CVR) that entitles the holder to receive up to an aggregate of $9.00 subject to the achievement of three milestones described below, for total potential aggregate per share consideration of up to $47.00. CVR holders would become entitled to receive contingent payments as follows: (i) $2.00 per CVR in cash, upon U.S. FDA approval of cleminorexton (formerly ORX750) or ORX142 for the treatment of narcolepsy type 2 prior to the fifth anniversary of transaction closing; (ii) $5.00 per CVR in cash, upon U.S. FDA approval of cleminorexton (formerly ORX750) or ORX142 for the treatment of idiopathic hypersomnia prior to the fifth anniversary of transaction closing; and (iii) $2.00 per CVR in cash, upon the first U.S. FDA approval of cleminorexton (formerly ORX750) or ORX142 for the treatment of any indication prior to January 1, 2030. The agreement stipulates a $63.06 million termination fee payable by the target to the buyer. Entities affiliated with Medicxi Ventures, entities affiliated with Index Ventures, and affiliates of General Atlantic have signed voting and support agreements whereby they agree to vote to approve the transaction. The shares subject to the agreements represent a total of approximately 24.1% of Centessa’s outstanding ordinary shares (represented by ADSs). The transaction, which will be effectuated by way of a scheme of arrangement under the laws of England and Wales, subject to approval by Centessa shareholders, sanction by the High Court of Justice of England and Wales and satisfaction of other customary closing conditions, including regulatory and antitrust approvals. The boards of directors of both companies have approved the transaction. The transaction is expected to close in the third quarter of 2026. Morgan Stanley & Co. LLC acted as financial advisor for Eli Lilly and Company. Sarkis Jebejian, Keri Schick Norton, Steven M. Choi of Kirkland & Ellis LLP and Dipak Bhundia, Bonian Wu of Kirkland & Ellis International LLP acted as legal advisor for Eli Lilly and Company. Centerview Partners LLC and Jefferies LLC acted as financial advisors for Centessa Pharmaceuticals plc. Stuart M Cable, Lisa R Haddad, Blake Liggio of Goodwin Procter LLP acted as legal advisor for Centessa Pharmaceuticals plc.
Recent Insider Transactions Derivative • Mar 29Chief People Officer notifies of intention to sell stockKaren Anderson intends to sell 41k shares in the next 90 days after lodging an Intent To Sell Form on the 26th of March. If the sale is conducted around the recent share price of US$28.15, it would amount to US$1.2m. Since June 2025, Karen's direct individual holding has increased from 58.36k shares to 66.12k. Company insiders have collectively sold US$12m more than they bought, via options and on-market transactions in the last 12 months.
Recent Insider Transactions Derivative • Mar 15Chief People Officer notifies of intention to sell stockKaren Anderson intends to sell 120k shares in the next 90 days after lodging an Intent To Sell Form on the 13th of March. If the sale is conducted around the recent share price of US$25.86, it would amount to US$3.1m. Since June 2025, Karen's direct individual holding has increased from 58.36k shares to 76.75k. Company insiders have collectively sold US$8.6m more than they bought, via options and on-market transactions in the last 12 months.
Recent Insider Transactions • Feb 04General Counsel recently sold US$1.0m worth of stockOn the 2nd of February, Iqbal Hussain sold around 40k shares on-market at roughly US$25.15 per share. This transaction amounted to 61% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Insiders have been net sellers, collectively disposing of US$3.6m more than they bought in the last 12 months.
お知らせ • Dec 13+ 1 more updateCentessa Pharmaceuticals plc Announces CEO Changes, Effective January 1, 2026Centessa Pharmaceuticals plc announced that its Board of Directors has appointed Mario Alberto Accardi PhD, President and founder of Centessa’s Orexin Program, as Chief Executive Officer (CEO), effective January 1, 2026. Dr. Accardi will succeed Saurabh Saha MD PhD, who will step down from his position as CEO, effective January 1, 2026. Dr. Saha will be appointed advisor to the CEO. As President of Centessa’s Orexin Program, Dr. Accardi has been responsible for leading the advancement of the orexin pipeline, which has become the full focus of the Company. Prior to Centessa, he was founder and CEO of Orexia Therapeutics. At Orexia, he successfully raised a €40M Series A, established multiple strategic partnerships, and led the company through its successful acquisition by Centessa in 2021. Dr. Accardi holds a Postgraduate in Genomic Medicine, a PhD in Biomedical Engineering and a First-Class Honours MEng Degree in Mechanical Engineering from Imperial College London.
Price Target Changed • Nov 20Price target increased by 7.3% to US$36.38Up from US$33.92, the current price target is an average from 13 analysts. New target price is 32% above last closing price of US$27.54. Stock is up 51% over the past year. The company is forecast to post a net loss per share of US$1.38 next year compared to a net loss per share of US$2.06 last year.
Recent Insider Transactions Derivative • Nov 16Chief Technology & Quality Officer exercised options and sold US$663k worth of stockOn the 12th of November, Tia Bush exercised 40k options at a strike price of around US$9.42 and sold these shares for an average price of US$26.00 per share. This trade did not impact their existing holding. Since December 2024, Tia's direct individual holding has decreased from 76.05k shares to 74.53k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.
お知らせ • Nov 12+ 1 more updateCentessa Pharmaceuticals plc has completed a Follow-on Equity Offering in the amount of $250.000001 million.Centessa Pharmaceuticals plc has completed a Follow-on Equity Offering in the amount of $250.000001 million. Security Name: American Depositary Shares Security Type: Depositary Receipt (Common Stock) Securities Offered: 11,627,907 Price\Range: $21.5 Discount Per Security: $1.29
分析記事 • Oct 28Health Check: How Prudently Does Centessa Pharmaceuticals (NASDAQ:CNTA) Use Debt?Howard Marks put it nicely when he said that, rather than worrying about share price volatility, 'The possibility of...
Buy Or Sell Opportunity • Sep 30Now 20% undervaluedOver the last 90 days, the stock has risen 76% to US$24.25. The fair value is estimated to be US$30.41, however this is not to be taken as a buy recommendation but rather should be used as a guide only. Revenue has grown by 102% over the last 3 years. Earnings per share has grown by 13%. For the next 3 years, revenue is forecast to grow by 73% per annum. Earnings are also forecast to grow by 24% per annum over the same time period.
Recent Insider Transactions Derivative • Sep 26Chief Technology & Quality Officer exercised options and sold US$510k worth of stockOn the 24th of September, Tia Bush exercised 35k options at a strike price of around US$9.42 and sold these shares for an average price of US$24.00 per share. This trade did not impact their existing holding. Since September 2024, Tia's direct individual holding has decreased from 78.08k shares to 74.53k. Company insiders have collectively sold US$15m more than they bought, via options and on-market transactions in the last 12 months.
Recent Insider Transactions Derivative • Sep 14Chief Technology & Quality Officer exercised options and sold US$612k worth of stockOn the 10th of September, Tia Bush exercised 50k options at a strike price of around US$8.01 and sold these shares for an average price of US$20.30 per share. This trade did not impact their existing holding. Since September 2024, Tia's direct individual holding has decreased from 78.08k shares to 74.53k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.
Buy Or Sell Opportunity • Jul 31Now 23% overvalued after recent price riseOver the last 90 days, the stock has risen 26% to US$17.17. The fair value is estimated to be US$13.97, however this is not to be taken as a sell recommendation but rather should be used as a guide only. Revenue has grown by 107% over the last 3 years. Earnings per share has grown by 14%. For the next 3 years, revenue is forecast to grow by 67% per annum. Earnings are also forecast to grow by 21% per annum over the same time period.
Recent Insider Transactions Derivative • Jul 23CEO & Director exercised options and sold US$664k worth of stockOn the 21st of July, Saurabh Saha exercised 55k options at a strike price of around US$3.85 and sold these shares for an average price of US$15.92 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 12% salary and 88% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since September 2024, Saurabh's direct individual holding has decreased from 345.91k shares to 90.33k. Company insiders have collectively sold US$15m more than they bought, via options and on-market transactions in the last 12 months.
分析記事 • Jul 17Centessa Pharmaceuticals (NASDAQ:CNTA) Is Using Debt SafelyLegendary fund manager Li Lu (who Charlie Munger backed) once said, 'The biggest investment risk is not the volatility...
Recent Insider Transactions Derivative • Jun 22CEO & Director exercised options and sold US$483k worth of stockOn the 20th of June, Saurabh Saha exercised 55k options at a strike price of around US$3.85 and sold these shares for an average price of US$12.63 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 12% salary and 88% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since June 2024, Saurabh's direct individual holding has decreased from 417.17k shares to 90.33k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.
お知らせ • Jun 18Centessa Pharmaceuticals plc Announces Clearance of Investigational New Drug Application for ORX142Centessa Pharmaceuticals plc announced that the U.S. Food and Drug Administration (FDA) has cleared the IND to initiate a Phase 1 clinical study of ORX142 in healthy volunteers. ORX142 is an investigational, novel, highly potent and selective OX2R agonist being developed for the treatment of select neurological and neurodegenerative disorders. ORX142 is the second drug candidate from the Company’s multi-asset orexin franchise. The Phase 1 study will evaluate the safety, tolerability and pharmacokinetics of single-ascending doses (SAD) and multiple-ascending doses (MAD) of ORX142 in healthy volunteers. In parallel to the SAD, a placebo-controlled crossover pharmacodynamic (PD) assessment will be performed utilizing the Maintenance of Wakefulness Test (MWT) and Karolinska Sleepiness Scale (KSS) in acutely sleep-deprived healthy adult subjects. The Company plans to initiate the first-in-human Phase 1 clinical study imminently, with clinical data expected 2025.
Recent Insider Transactions Derivative • May 21CEO & Director exercised options and sold US$487k worth of stockOn the 20th of May, Saurabh Saha exercised 55k options at a strike price of around US$3.85 and sold these shares for an average price of US$12.71 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 12% salary and 88% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since June 2024, Saurabh's direct individual holding has decreased from 417.17k shares to 45.17k. Company insiders have collectively sold US$14m more than they bought, via options and on-market transactions in the last 12 months.
Recent Insider Transactions • Apr 24CEO & Director recently sold US$682k worth of stockOn the 22nd of April, Saurabh Saha sold around 55k shares on-market at roughly US$12.39 per share. This transaction amounted to 55% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger sale worth US$918k. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$6.1m.
お知らせ • Apr 23Centessa Pharmaceuticals plc, Annual General Meeting, Jun 20, 2025Centessa Pharmaceuticals plc, Annual General Meeting, Jun 20, 2025. Location: offices of goodwin procter (uk) llp at sancroft, 10-15 newgate street, london, ec1a 7az, United Kingdom
Price Target Changed • Mar 31Price target increased by 9.4% to US$31.25Up from US$28.57, the current price target is an average from 8 analysts. New target price is 117% above last closing price of US$14.38. Stock is up 30% over the past year. The company is forecast to post a net loss per share of US$1.53 next year compared to a net loss per share of US$2.06 last year.
New Risk • Mar 24New major risk - Revenue sizeThe company makes less than US$1m in revenue. This is considered a major risk. Companies with a small amount of revenue are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Shareholders have been substantially diluted in the past year (35% increase in shares outstanding). Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$260m net loss in 3 years). Significant insider selling over the past 3 months (US$3.0m sold).
Recent Insider Transactions • Mar 23CEO & Director recently sold US$918k worth of stockOn the 20th of March, Saurabh Saha sold around 55k shares on-market at roughly US$16.69 per share. This transaction amounted to 35% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$5.4m.
Price Target Changed • Mar 14Price target increased by 9.3% to US$30.29Up from US$27.71, the current price target is an average from 7 analysts. New target price is 77% above last closing price of US$17.14. Stock is up 59% over the past year. The company is forecast to post a net loss per share of US$1.62 next year compared to a net loss per share of US$1.57 last year.
Buy Or Sell Opportunity • Mar 07Now 22% undervalued after recent price dropOver the last 90 days, the stock has fallen 13% to US$16.23. The fair value is estimated to be US$20.80, however this is not to be taken as a buy recommendation but rather should be used as a guide only. Revenue has grown by 129% over the last 3 years. Earnings per share has grown by 36%. For the next 3 years, revenue is forecast to grow by 71% per annum. Earnings are also forecast to grow by 13% per annum over the same time period.
Recent Insider Transactions • Feb 23CEO & Director recently sold US$876k worth of stockOn the 20th of February, Saurabh Saha sold around 55k shares on-market at roughly US$15.93 per share. This transaction amounted to 26% of their direct individual holding at the time of the trade. In the last 3 months, there was an even bigger sale from another insider worth US$1.2m. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$4.5m.
Recent Insider Transactions Derivative • Feb 09Chief People Officer notifies of intention to sell stockKaren Anderson intends to sell 31k shares in the next 90 days after lodging an Intent To Sell Form on the 7th of February. If the sale is conducted around the recent share price of US$19.03, it would amount to US$581k. Since March 2024, Karen's direct individual holding has decreased from 77.69k shares to 54.32k. Company insiders have collectively sold US$10m more than they bought, via options and on-market transactions in the last 12 months.
Recent Insider Transactions • Jan 23CEO & Director recently sold US$867k worth of stockOn the 21st of January, Saurabh Saha sold around 55k shares on-market at roughly US$15.77 per share. This transaction amounted to 25% of their direct individual holding at the time of the trade. In the last 3 months, there was an even bigger sale from another insider worth US$1.2m. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$3.6m.
New Risk • Jan 16New major risk - Shareholder dilutionThe company's shareholders have been substantially diluted in the past year. Increase in shares outstanding: 35% This is considered a major risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risk Shareholders have been substantially diluted in the past year (35% increase in shares outstanding). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$240m net loss in 3 years). Significant insider selling over the past 3 months (US$4.3m sold).
Buy Or Sell Opportunity • Jan 10Now 21% undervalued after recent price dropOver the last 90 days, the stock has fallen 2.2% to US$15.64. The fair value is estimated to be US$19.80, however this is not to be taken as a buy recommendation but rather should be used as a guide only. Revenue has grown by 129% over the last 3 years. Earnings per share has grown by 36%. For the next 3 years, revenue is forecast to grow by 71% per annum. Earnings are also forecast to grow by 14% per annum over the same time period.
お知らせ • Jan 08Centessa Pharmaceuticals Announces Appointment of Stephen Kanes as Chief Medical OfficerCentessa Pharmaceuticals plc announced the appointment of Stephen Kanes MD PhD, as Chief Medical Officer (CMO). Dr. Kanes is a neuropsychiatrist, with a career in neuroscience, clinical psychiatry, and neuroscience drug development spanning more than 30 years. Dr. Kanes served as Chief Medical Officer of Sage Therapeutics from 2013 to 2021, where he led the successful clinical development of ZULRESSO® (brexanolone), the first-ever treatment approved for Postpartum Depression (PPD), along with the buildout of the development organization and Sage Therapeutics' broad neuroscience portfolio. Most recently, Dr. Kanes was Chief Executive Officer of EmbarkNeuro, a neuroscience focused biotech company. Earlier in his career, Dr. Kanes was Executive Director in Clinical Development in the Inflammation, Neuroscience and Respiratory therapeutic areas at AstraZeneca, and a faculty member of the University of Pennsylvania Department of Psychiatry where he explored both the genetics and physiology of severe mental illness. He has authored or co-authored more than 60 peer-reviewed publications in behavioral neuroscience, behavioral pharmacology, genetics, brain imaging, clinical trials, and health economics and serves as an ad hoc reviewer for multiple journals including Neuropsychopharmacology andThe American Journal of Medical Genetics and Biological Psychiatry. Dr. Kanes received his BA from the University of Pennsylvania in the Biological Basis of Behavior and both his PhD in Molecular and Cellular Pharmacology and MD from the Stony Brook University Renaissance School of Medicine. He completed his psychiatry residency at Yale-New Haven Medical Center and a neuropsychiatry postdoctoral fellowship at the University of Pennsylvania.
Seeking Alpha • Dec 31Centessa Pharmaceuticals: Orexin Franchise Worth MonitoringSummary Centessa Pharmaceuticals, founded from the merger of 10 biotech companies, is based on an asset-centric model, primarily developing its lead orexin agonist, ORX-750. ORX-750 targets narcolepsy types 1 and 2 and idiopathic hypersomnia, showing promising phase 1 results, with phase 2 data expected in 2025. Takeda's TAK-861 success partially de-risks ORX-750, making Centessa a potential acquisition target if ORX-750 proves it is best-in-class. With $500M in cash and a runway into mid-2027, Centessa's phase 2 trial results for ORX-750 are crucial for its future valuation. Read the full article on Seeking Alpha
Recent Insider Transactions • Dec 19General Counsel recently sold US$1.2m worth of stockOn the 16th of December, Iqbal Hussain sold around 72k shares on-market at roughly US$16.39 per share. This transaction amounted to 76% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Insiders have been net sellers, collectively disposing of US$3.6m more than they bought in the last 12 months.
Recent Insider Transactions Derivative • Dec 09CEO & Director exercised options and sold US$1.1m worth of stockOn the 6th of December, Saurabh Saha exercised 87k options at a strike price of around US$5.84 and sold these shares for an average price of US$18.46 per share. This trade did not impact their existing holding. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since December 2023, Saurabh's direct individual holding has increased from 313.17k shares to 526.82k. Company insiders have collectively sold US$6.0m more than they bought, via options and on-market transactions in the last 12 months.
Recent Insider Transactions • Nov 25CEO & Director recently sold US$929k worth of stockOn the 20th of November, Saurabh Saha sold around 55k shares on-market at roughly US$16.89 per share. This transaction amounted to 19% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. Saurabh has been a net seller over the last 12 months, reducing personal holdings by US$1.8m.
New Risk • Nov 20New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 2.1% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risk Earnings are forecast to decline by an average of 2.1% per year for the foreseeable future. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$237m net loss in 3 years). Shareholders have been diluted in the past year (35% increase in shares outstanding). Significant insider selling over the past 3 months (US$1.3m sold).
Price Target Changed • Nov 17Price target increased by 8.2% to US$28.29Up from US$26.14, the current price target is an average from 7 analysts. New target price is 77% above last closing price of US$16.00. Stock is up 127% over the past year. The company is forecast to post a net loss per share of US$1.66 next year compared to a net loss per share of US$1.57 last year.
お知らせ • Nov 13Centessa Pharmaceuticals Initiates Phase 2 Trial with ORX750, a Novel Orexin Receptor 2 (OX2R) AgonistNxera Pharma Co. Ltd. announced that Centessa Pharmaceuticals has initiated a Phase 2 trial of ORX750, an investigational, orally administered, highly potent and selective orexin receptor 2 (OX2R) antagonist for the treatment of narcolepsy type 1 (NT1), narcolepsy type 2 (NT2), and idiopathic hypersomnia. The achievement of this milestone results in a payment of USD 3.5 million to Nxera pursuant to its research collaboration with Centessa. This will be recognised as revenue in Fourth Quarter Fiscal Year 2024. ORX750 was designed using Nxera technology to directly target the underlying pathophysiology of orexin neuron loss in NT1, with potential applicability to NT2, idiopathic hypersomnia, and other sleep- wake disorders with normal orexin levels.
Recent Insider Transactions • Oct 25CEO & Director recently sold US$864k worth of stockOn the 23rd of October, Saurabh Saha sold around 55k shares on-market at roughly US$15.70 per share. This transaction amounted to 16% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. This was Saurabh's only on-market trade for the last 12 months.
Recent Insider Transactions Derivative • Oct 24CEO & Director notifies of intention to sell stockSaurabh Saha intends to sell 22k shares in the next 90 days after lodging an Intent To Sell Form on the 21st of October. If the sale is conducted around the recent share price of US$15.80, it would amount to US$351k. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since December 2023, Saurabh's direct individual holding has increased from 313.17k shares to 708.09k. Company insiders have collectively sold US$2.7m more than they bought, via options and on-market transactions in the last 12 months.
Recent Insider Transactions • Sep 29Chief Business Officer recently sold US$261k worth of stockOn the 25th of September, Gregory Weinhoff sold around 17k shares on-market at roughly US$15.69 per share. This transaction amounted to 19% of their direct individual holding at the time of the trade. This was the largest sale by an insider in the last 3 months. This was the only on-market transaction from insiders over the last 12 months.
Seeking Alpha • Sep 25Centessa Pharmaceuticals: Progressing SerpinPC Through Registrational Trials In Hemophilia BSummary Centessa Pharma's SerpinPC, a subcutaneous biologic inhibitor, shows promising results in reducing bleeding rates in hemophilia B, with a favorable safety profile. Despite the stock doubling in value, I remain cautious due to the company's unclear business strategy and lack of registrational data. The hemophilia B market is competitive with existing treatments. SerpinPC's unique mechanism and delivery method provide niche advantages but face significant competition. With a $2bn market cap and a cash runway of 6-7 quarters, I will avoid investing until there's more clarity on their strategic direction. Read the full article on Seeking Alpha
Recent Insider Transactions Derivative • Sep 23CEO & Director notifies of intention to sell stockSaurabh Saha intends to sell 55k shares in the next 90 days after lodging an Intent To Sell Form on the 20th of September. If the sale is conducted around the recent share price of US$16.45, it would amount to US$905k. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since September 2023, Saurabh's direct individual holding has increased from 274.44k shares to 724.35k. Company insiders have collectively sold US$2.4m more than they bought, via options and on-market transactions in the last 12 months.
お知らせ • Sep 12Centessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $150 million.Centessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $150 million. Security Name: American Depositary Shares Security Type: Depositary Receipt (Common Stock)
Recent Insider Transactions Derivative • Sep 11Chief Business Officer notifies of intention to sell stockGregory Weinhoff intends to sell 25k shares in the next 90 days after lodging an Intent To Sell Form on the 9th of September. If the sale is conducted around the recent share price of US$15.00, it would amount to US$375k. Since September 2023, Gregory's direct individual holding has increased from 76.64k shares to 206.44k. There have been no trades via on-market transactions or options from company insiders in the last 12 months.
Price Target Changed • Sep 10Price target increased by 10% to US$16.00Up from US$14.50, the current price target is an average from 6 analysts. New target price is 9.7% above last closing price of US$14.58. Stock is up 117% over the past year. The company is forecast to post a net loss per share of US$1.61 next year compared to a net loss per share of US$1.57 last year.
お知らせ • Sep 10Centessa Pharmaceuticals plc Announces Positive Interim Phase 1 Clinical Data with Its Novel Orexin Receptor 2 (OX2R) Agonist, Orx750, in Acutely Sleep-Deprived Healthy VolunteersCentessa Pharmaceuticals plc announced positive interim data from an ongoing Phase 1 trial of its highly potent and selective orexin receptor 2 (OX2R) agonist, ORX750, in acutely sleep-deprived healthy volunteers. ORX750 showed clinically meaningful and statistically significant improvements in mean sleep latency at the first two doses evaluated (1.0 mg and 2.5 mg) in the Maintenance of Wakefulness Test (MWT) compared to placebo. More specifically, the 2.5 mg dose was shown to restore normative wakefulness2 with a mean sleep latency of 32 minutes as measured by the MWT. ORX750 was also shown to have a favorable safety and tolerability profile with no observations of frequently reported on-target adverse events (AEs) associated with other OX2R agonists, and no cases of hepatotoxicity or visual disturbances across all three dose levels tested (1.0 mg, 2.0 mg, and 2.5 mg), as of the data cutoff date.1 Based on the interim data, the Company plans to rapidly advance ORX750 into Phase 2 studies in patients with narcolepsy type 1 (NT1), narcolepsy type 2 (NT2), and idiopathic hypersomnia (IH) beginning in the fourth quarter of 2024. The Phase 1 clinical study is an ongoing first-in-human, randomized, placebo-controlled study designed to evaluate the safety, tolerability and pharmacokinetics (PK) of single-ascending doses (SAD) and multiple-ascending doses (MAD) of ORX750 in healthy adult subjects. In parallel to the SAD, a placebo-controlled cross-over pharmacodynamic (PD) assessment is being performed utilizing the MWT and Karolinska Sleepiness Scale (KSS) in acutely sleep-deprived healthy adult subjects with the goal of rapidly generating early efficacy data to inform dosing for planned studies in patients. As of September 10, 2024, the study has completed three SAD cohorts of healthy volunteers (27 active, 9 placebo) with doses of 1.0 mg, 2.0 mg, and 2.5 mg, and has advanced through two cohorts within the cross-over assessment of acutely sleep-deprived healthy volunteers with doses of 1.0 mg (n=8) and 2.5 mg (n=8), administered as a single oral dose. Dosing in the MAD portion of the study is also ongoing.
Recent Insider Transactions Derivative • Aug 26CEO & Director notifies of intention to sell stockSaurabh Saha intends to sell 47k shares in the next 90 days after lodging an Intent To Sell Form on the 23rd of August. If the sale is conducted around the recent share price of US$12.30, it would amount to US$574k. For the year to December 2021, Saurabh's total compensation was 24% salary and 76% other compensation. This indicates that these sales could comprise a meaningful part of their income for the year. Since September 2023, Saurabh's direct individual holding has increased from 274.44k shares to 333.83k. There have been no trades via on-market transactions or options from company insiders in the last 12 months.
Price Target Changed • Jun 21Price target increased by 9.2% to US$14.20Up from US$13.00, the current price target is an average from 5 analysts. New target price is 60% above last closing price of US$8.86. Stock is up 34% over the past year. The company is forecast to post a net loss per share of US$1.63 next year compared to a net loss per share of US$1.57 last year.
お知らせ • Jun 13+ 1 more updateCentessa Pharmaceuticals plc Announces Chief Financial Officer ChangesOn June 10, 2024, Centessa Pharmaceuticals plc (the Company) announced the appointment of John Crowley as Chief Financial Officer, which was approved by the Board of Directors of the Company on June 5, 2024, effective June 10, 2024 (the Start Date). Accordingly, Mr. Crowley has also been designated the Company’s principal financial officer and principal accounting officer, replacing Dr. Gregory Weinhoff as Chief Financial Officer and in those roles. John Crowley CPA, Chief Financial Officer: Mr. Crowley brings over 20 years of global finance and operational experience in the life sciences industry to Centessa. He most recently served as Chief Financial Officer of Fusion Pharmaceuticals prior to its acquisition by AstraZeneca in June 2024. He also served as Executive Vice President and Chief Financial Officer of Merus Inc. Prior to Merus, Mr. Crowley served as the Corporate Senior Vice President, Corporate Controller and Chief Accounting Officer of Charles River Laboratories Inc. Previously, Mr. Crowley held senior corporate finance positions at Ironwood Pharmaceuticals Inc., Vertex Pharmaceuticals Inc., and Sunovion Pharmaceuticals Inc., where he supported several commercial launches, financings, and business development transactions in rapidly growing companies. Mr. Crowley is a Certified Public Accountant and graduated Summa Cum Laude from Babson College with BS degrees in both Economics and Accountancy. Dr. Weinhoff served as Chief Financial Officer of Centessa from March 2021 to June 2024. He brings over 20 years of business development experience to the newly created position of Chief Business Officer. Prior to Centessa, Dr. Weinhoff was co-founder, director and chief financial and business officer of Arvelle Therapeutics B.V., which was acquired by Angelini Pharma in 2021. While with Arvelle, he led the asset identification and in-licensing of cenobamate, a novel anti-seizure medicine. Prior to Arvelle, Dr. Weinhoff served as Chief Financial Officer at Axovant Sciences Inc., where he led financial functions and the execution of several private and public financings. Before Axovant, Dr. Weinhoff spent 15 years as an early-stage healthcare venture capitalist at CHL Medical Partners, where he was founding CEO of Amicus Therapeutics and his firm was the sole Series A investor. Dr. Weinhoff holds an MD from Harvard Medical School, an MBA from Harvard Business School and an AB in economics from Harvard College. Prior to graduate school, Dr. Weinhoff was a financial analyst in Morgan Stanley & Co.’s healthcare corporate finance group.
Board Change • Jun 02Insufficient new directorsThere is 1 new director who has joined the board in the last 3 years. The company's board is composed of: 1 new director. 7 experienced directors. No highly experienced directors. Independent Non-Executive Director Mathias Hukkelhoven was the last director to join the board, commencing their role in 2022. The company’s insufficient board refreshment is considered a risk according to the Simply Wall St Risk Model.
お知らせ • Apr 25+ 1 more updateCentessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $100 million.Centessa Pharmaceuticals plc has filed a Follow-on Equity Offering in the amount of $100 million. Security Name: American Depositary Shares Security Type: Depositary Receipt (Common Stock)
Seeking Alpha • Apr 24Centessa: Hemophilia B Data Readout In 2024 Is Major Turning PointSummary Centessa Pharmaceuticals plc interim data from the PRESent-2 study, using SerpinPC for the treatment of patients with Hemophilia B without inhibitors, is expected to be released in 2024. PRESent-3 is another registrational study using SerpinPC for the treatment of patients with Hemophilia B, however it is for the targeting of such patients with inhibitors. ORX750 is an oral selective orexin receptor agonist being developed for the treatment of patients with Narcolepsy Type 1; Proof of concept data to be released in second half 2024. LB101 is another product in the pipeline with great potential targeting solid tumors, because it utilizes proven targeted proteins such as PD-L1 and CD47; The PD-L1 blockade occurs first as a block mechanism then with hinges dissolving moves the CD47 into place to perform mechanism of action. Read the full article on Seeking Alpha
お知らせ • Apr 23Centessa Pharmaceuticals plc Announces Open IND for ORX750Centessa Pharmaceuticals plc announced that the U.S. Food and Drug Administration (FDA) has cleared the Investigational New Drug application (IND) to initiate a Phase 1 first-in-human, clinical trial of ORX750 for the treatment of narcolepsy. ORX750 is an investigational, orally administered, highly potent and selective orexin receptor 2 (OX2R) agonist designed to directly target the underlying pathophysiology of orexin neuron loss in narcolepsy type 1 (NT1), with potential applicability to narcolepsy type 2 (NT2), idiopathic hypersomnia (IH), and other sleep-wake disorders with normal orexin levels. The Phase 1 study will evaluate the safety, tolerability and pharmacokinetics of single-ascending doses (SAD) and multiple-ascending doses (MAD) of ORX750 in healthy adult subjects. In parallel to the SAD, a cross-over pharmacodynamic (PD) assessment will be performed utilizing the Maintenance of Wakefulness Test (MWT) and Karolinska Sleepiness Scale (KSS) in acutely sleep-deprived healthy adult subjects which is intended to provide proof-of-concept data to enable dose selection for NT1, NT2 and IH indications. The study has a maximum exposure limit specified by the FDA which the Company believes significantly exceeds the predicted efficacious doses of ORX750 in indications associated with or without orexin loss; therefore, the Company does not expect this limit to affect any of the planned clinical development activities for ORX750. The Company expects to commence dosing of the Phase 1 study in healthy volunteers imminently, and proof-of-concept data are anticipated in the second half of 2024. ORX750 is an investigational, orally administered, highly potent and selective orexin receptor 2 (OX2R) agonist designed to directly target the underlying pathophysiology of orexin neuron loss in narcolepsy type 1 (NT1). ORX750 has been shown to potently activate the OX2R with an in vitro EC50 of 0.11 nM and 9,800-fold selectivity over the human orexin receptor (hOX1R). ORX750 is Centessa’s first orexin product candidate being developed for the treatment of narcolepsy with potential expansion into narcolepsy type 2 (NT2), idiopathic hypersomnia (IH) and other sleep-wake disorders.
New Risk • Mar 05New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 0.3% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 0.3% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$218m net loss in 3 years). Share price has been volatile over the past 3 months (12% average weekly change). Shareholders have been diluted in the past year (3.2% increase in shares outstanding).
お知らせ • Dec 11Centessa Pharmaceuticals plc Announces New Data from an Additional 52-Weeks of Continuous Treatment from Third Year (Part 5) of Ongoing Phase 2A Study of Serpinpc for the Treatment of HemophiliaCentessa Pharmaceuticals plc announced new data from an additional 52-we weeks of continuous treatment from the third year (Part 5) of the ongoing Phase 2a study of SerpinPC for the treatment of hemophilia. The data were shared in a poster presentation at the American Society of Hematology (ASH) Annual Meeting on December 10, 2023. During treatment with SerpinPC all breakthrough bleeds were treated on-demand w ith usual clotting factor concentrate, without dose reduction and without limitation of number of infusions. Data from Part 5 were presented at the ASH Annual Meeting in a poster titled: SerpinPC in persons with severe hemophilia (PwH): Updated results from a multi-center, multi-part, first-in-human study.
お知らせ • Nov 01Centessa Pharmaceuticals plc Announces Dosing of First Subject in Registrational Present-3 Study Evaluating Serpinpc for the Treatment of Hemophilia B with InhibitorsCentessa Pharmaceuticals plc announced the dosing of the first subject in its registrational Present-3 study of SerpinPC for the treatment of hemophilia B with inhibitors. The dosing phase of Present-3 follows a minimum 12-week observation period during which prospective baseline data of the subject's disease status under their current therapy are collected to support regulatory review of the benefit and risk profile of SerpinPC. SerpinPC is a subcutaneously administered novel inhibitor of APC being developed as a potential treatment for hemophilia, regardless of severity or inhibitor status, and which may also be developed to prevent bleeding associated with other bleeding disorders. The registrational program for SerpinPC in hemophilia B includes a set of clinical studies with multiple components. Present-5 is an observational feeder study to collect prospective observational data for minimum defined periods before switching to dosing subjects in the interventional studies. The U.S. Food and Drug Administration (FDA) has granted Fast Track designation to SerpinPC for the treatmentof hemophilia B, with or without inhibitors. SerpinPC is an investigational agent that has not been approved by the FDA or any other regulatory authority.
お知らせ • Oct 26Centessa Pharmaceuticals plc Announces Preclinical Data Supporting Orx750's Potential as A Best-In-Class Oral Ox2r Agonist for the Treatment of Narcolepsy and Other Sleep-Wake DisordersCentessa Pharmaceuticals plc announced a robust set of new preclinical data from in vivo and in vitro studies of its investigational, novel orexin receptor 2 (OX2R) agonist, ORX750, that support its potential best-in-class profile for the treatment of narcolepsy and other sleep- wake disorders. ORX750 is an investigational, orally administered, highly potent and selective orexin receptor 2 (ox2R) agonist designed to directly target the underlying pathophysiology of orexin neuron loss in narcolepsy type 1 (NT1). ORX750 is Centessa's first orexin product candidate being developed for the treatment of narcolpsy with potential expansion into other sleep- wake disorders.ORX750 is currently undergoing IND-enabling activities and has not been administered as an investigational drug to humans in any jurisdiction. Any such statements that are not statements of historical fact may be deemed to be forward-looking statements, including statements related to: the Company's ability to deliver transformational medicines to patients; the activity significance of low doses in highly predictive, translational models of narcolepsy type 1 ("NT1") including maximal wake times and suppressed cataplexy at the lowest oral dose tested; the Company's expectations on the timing of Ind-enabling studies of ORX750 in narcolepsy and other Sleep- wake disorders; the ability of management team and board to drive execution of the Company's portfolio of programs; asset-centric business model and the intended advantages and benefits thereof; the scope, progress, results and costs of developing product candidates or any other future product candidates; current expectations concerning, amongst other things, the development and therapeutic potential and benefits of product candidates, including ORX750 and other OX2R agonists; strategy; regulatory matters, including the timing and likelihood of initiating clinical trials, reporting clinical trial results, ability to initiate or continue clinical trials or market any products; and the market size and opportunity for product candidates. Based on current expectations, estimates and projections only as of the date of this release and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set out in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, risks related to the safety and tolerability profile of product candidates including ORX750; ability to protect and maintain intellectual property position; business (including commercial viability), regulatory, economic and competitive risks, uncertainties, contingencies and assumptions about the Company; risks inherent in developing product candidates and technologies; ability to obtain adequate financing, including through financing facility with Oberland, to fund planned clinical trials and other expenses; trends in the industry; the legal and regulatory framework for the industry, including the receipt and maintenance of clearances to conduct or continue clinical testing; future expenditures risks related to asset-centric corporate model; the risk that any one or more of product candidates will not be successfully developed and/or commercialized; and the risk that the results of non-clinical studies or clinical studies will not be predictive of future results.
Recent Insider Transactions Derivative • Sep 22Insider notifies of intention to sell stockHarris Rotman intends to sell 37k shares in the next 90 days after lodging an Intent To Sell Form on the 20th of September. If the sale is conducted around the recent share price of US$6.50, it would amount to US$244k. Since June 2023, Harris has owned 33.50k shares directly. There have been no trades via on-market transactions or options from company insiders in the last 12 months.
お知らせ • Aug 25World Sleep Congress Releases an Abstract Submit by Centessa Pharmaceuticals plcOn August 22, 2023, the World Sleep Congress 2023 released an abstract submitted by Centessa Pharmaceuticals Plc. containing preclinical data on ORX750, the company's orally administered, selective orexin receptor 2 (OX2R) agonist in development for the treatment of narcolepsy and other sleep disorders. The company will present the abstract in an oral presentation on October 25, 2023. Introduction: Narcolepsy Type 1 (NT1) is a rare neurological disease caused by the profound loss of orexin-producing neurons. Orexin (also called hypocretin) is a neurotransmitter that regulates wakefulness, arousal, and energy homeostasis via activation of Orexin Receptor-1 (OX1R) and -2 (OX2R). Orexin agonists are designed to directly address the underlying disease pathology of NT1 to restore orexin neurotransmission in the brain. The orexin/ataxin-3 (Atax) mouse model of NT1 recapitulates key features of the human disorder, such as orexin loss, inability to sustain wakefulness, and cataplexy (emotionally triggered, transient loss of muscle tone). Here it present ORX750, a novel, orally available, brain penetrant, OX2R selective agonist. ORX750 was developed using structure-based drug design with an OX2R stabilized receptor (StaR®) protein and high-resolution protein crystallography. Materials and Methods: In vitro calcium mobilization (FLIPR), ß-arrestin recruitment, and inositol-phosphate accumulation assays were performed in Chinese hamster ovary (CHO) cells stably expressing human recombinant OX1R or OX2R. Electrophysiological recordings were performed on slices of the ventral tuberomammillary nucleus (TMN) from mouse hypothalamus; effects on membrane potential were measured in the presence of 1 micromolar tetrodotoxin to block neuron firing. In vivo efficacy for enhancing wakefulness was evaluated in wild type (WT) and Atax mice during their rest phase using PiezoSleep, a rapid, non-invasive method for classifying sleep and wakefulness by unsupervised machine learning on physiologically relevant readouts, including body movement and breath rate. Electroencephalogram (EEG), electromyogram (EMG), and video recordings were used in Atax mice during their active phase to evaluate effects at 0.3-10 mg/kg on arousal states and cataplexy. Results: ORX750 behaved as a potent full agonist at human OX2R (EC50=0.11 nM) relative to the native ligand orexin A (OXA; EC50=0.035 nM) and showed 9,800-fold selectivity over human OX1R (EC50=1100 nM) in the FLIPR assay. Biased agonism was not detected by measurement of b-arrestin recruitment at OX2R in comparison to OXA. ORX750 depolarized membrane potential (EC50=5.0 nM, max DmV=9.5) in whole cell current-clamp recordings in the TMN. In the PiezoSleep assay, in which wakefulness readouts are highly correlated with EEG/EMG-defined wakefulness, ORX750 increased time awake and the consolidation of wakefulness vs. vehicle in a dose-related manner when administered to WT and Atax mice during the rest phase. Increased sensitivity to these wake-promoting effects was observed in Atax vs. WT mice. In Atax mice, ORX750 increased time awake; consolidated wakefulness; increased EEG gamma power during wakefulness; reduced cataplexy occurrences; and increased latencies to sleep and cataplexy in a dose-related manner during the active phase using the EEG/EMG/video assay. At the lowest dose tested (0.3 mg/kg) and compared to vehicle, the latency to sleep was 2.3 h vs. 0.69 h and the latency to cataplexy was 2.7 h vs. 1.3 h. Conclusions: ORX750 is an oral, highly potent, and selective OX2R agonist with the potential to treat patients with primary symptoms of NT1, as well as reduce excessive sleepiness in those presenting sleep/wake disorders with normal orexin levels.
New Risk • Aug 14New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 0.5% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 0.5% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$233m net loss in 3 years). Share price has been volatile over the past 3 months (14% average weekly change).
Price Target Changed • Jul 25Price target increased by 18% to US$7.08Up from US$6.00, the current price target is an average from 6 analysts. New target price is approximately in line with last closing price of US$7.14. Stock is up 62% over the past year. The company is forecast to post a net loss per share of US$1.99 next year compared to a net loss per share of US$2.31 last year.
お知らせ • Jul 12Centessa Pharmaceuticals Announces Dosing of First Subject in Registrational PRESent-2 Study Evaluating SerpinPC for the Treatment of Hemophilia B Without InhibitorsCentessa Pharmaceuticals plc announced the dosing of the first subject in its registrational PRESent-2 study of SerpinPC for the treatment of hemophilia B without inhibitors. The dosing phase of PRESent-2 follows a minimum 12-week observation period during which prospective baseline data of the subject’s disease status under their current therapy are collected to support regulatory review of the benefit and risk profile of SerpinPC. SerpinPC is an investigational subcutaneously administered novel inhibitor of activated protein C (APC) being developed as a potential treatment for hemophilia B, with or without inhibitors. The PRESent-2 study (AP-0102) is a Phase 2b, global, open-label, seamless adaptive design study to investigate the efficacy and safety of subcutaneous dosing of SerpinPC every week, every 2 weeks, or every 4 weeks in approximately 120 adult (aged 18 to =65 years) or adolescent (aged =12 to <18 years) male subjects with severe hemophilia A (with or without inhibitors) or moderately severe to severe hemophilia B (without inhibitors). PRESent-2 consists of 3 parts: a 24-week randomized dose-justification phase (Part 1), a 24-week dose-confirmatory phase (Part 2), and a further 24-week extension phase (Part 3) for subjects who complete either Part 1 or Part 2. Subjects must have undergone a minimum period of prospective observation (at least 12 weeks for Part 1 or 24 weeks for Part 2) under their current therapy (either on-demand or prophylaxis factor replacement) before switching to SerpinPC treatment. The primary efficacy endpoint for the study is the rate of treated bleeds (expressed as an annualized bleeding rate (ABR)) in the observation period compared to the first 24 weeks treated with SerpinPC. The Company expects to begin dosing in its registrational PRESent-3 (AP-0103) study for subjects with hemophilia B with inhibitors this year.
New Risk • Jul 06New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of American stocks, typically moving 10% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$235m net loss in 3 years). Share price has been volatile over the past 3 months (10% average weekly change).
お知らせ • May 23Centessa Pharmaceuticals Receives Fast Track Designation from the U.S. FDA for Serpinpc for Hemophilia BCentessa Pharmaceuticals plc announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to SerpinPC, an investigational novel inhibitor of activated protein C (APC) being developed for the treatment of hemophilia B, with or without inhibitors. According to the FDA, Fast Track is a process designed to facilitate the development and expedite the review of drug candidates to treat serious conditions and fulfill an unmet medical need. A therapeutic candidate that receives Fast Track designation may be eligible for more frequent interactions with the FDA to discuss the candidate’s development plan and, if relevant criteria are met, eligibility for Accelerated Approval, Priority Review, or Rolling Review.
お知らせ • Jan 27Centessa Pharmaceuticals Announces FDA Clearance of IND Application for Phase 1/2a Clinical Trial of LB101, First LockBody® Candidate, for Solid TumorsCentessa Pharmaceuticals plc announced that it has received clearance of its Investigational New Drug (IND) application from the U.S. Food and Drug Administration (FDA) to initiate a Phase 1/2a first-in-human, clinical trial of LB101 for the treatment of solid tumors. LB101, a conditionally tetravalent PD-L1xCD47 LockBody® bispecific monoclonal antibody targeting solid tumors, is the first product candidate developed using the Company’s proprietary LockBody technology which is designed to selectively drive potent effector function activity, such as CD47, in the tumor microenvironment (TME) while avoiding systemic toxicity.
Price Target Changed • Nov 16Price target decreased to US$6.00Down from US$9.50, the current price target is an average from 4 analysts. New target price is 70% above last closing price of US$3.53. Stock is down 72% over the past year. The company posted a net loss per share of US$5.07 last year.
Board Change • Nov 16High number of new and inexperienced directorsThere are 8 new directors who have joined the board in the last 3 years. The company's board is composed of: 8 new directors. No experienced directors. No highly experienced directors. Independent Chairman of the Board Francesco de Rubertis is the most experienced director on the board, commencing their role in 2020. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.
Seeking Alpha • Oct 20Centessa Pharmaceuticals snaps multi-day losing streak; up 10%For the first time since Oct. 13, Centessa Pharmaceuticals (NASDAQ:CNTA) is showing gains. In Thursday afternoon trading, the biotech is up 10%. There is no news or other catalysts that might explain the jump. However, based on a technical analysis, Centessa (CNTA) deviated two standard deviations lower from its mean touching its lower Bolinger Band level and has snapped up higher, back to its mean level. From market close Oct. 13 through market close Oct. 19, shares fell ~15%. Seeking Alpha views Centessa (CNTA) as a hold with high marks for valuation and growth.
Seeking Alpha • Sep 14Centessa hemophilia B therapy SerpinPC gets FDA orphan drug statusThe U.S. Food and Drug Administration (FDA) granted orphan drug designation to Centessa Pharmaceuticals' (NASDAQ:CNTA) SerpinPC to treat hemophilia B. The U.K.-based company said in a Sept. 14 press release that it plans to begin registrational studies of SerpinPC in Q4 2022. SerpinPC is a biological drug candidate, based on the serpin family of proteins which is designed to allow more thrombin to be generated by inhibiting activated protein C (APC), thus rebalancing coagulation in patients with hemophilia, according to Centessa. "We believe SerpinPC has the potential to offer patients with hemophilia B a convenient subcutaneous option that is designed to prevent and reduce bleeds without the risk of thrombosis," said Centessa CEO Saurabh Saha. The FDA grants orphan drug status to therapies which treat or prevent rare diseases that affect fewer than 200K people in the U.S. The designation provides certain incentives, including up to seven years of market exclusivity, if approved.
Seeking Alpha • Aug 10Centessa Pharmaceuticals GAAP EPS of -$0.69Centessa Pharmaceuticals press release (NASDAQ:CNTA): Q2 GAAP EPS of -$0.69. Cash and Cash Equivalents: $484.2 million as of June 30, 2022, which the Company expects will fund operations into 2026, without drawing on the remaining available tranches under the Oberland credit facility.
Board Change • Apr 27High number of new and inexperienced directorsThere are 8 new directors who have joined the board in the last 3 years. The company's board is composed of: 8 new directors. No experienced directors. No highly experienced directors. Independent Chairman of the Board Francesco de Rubertis is the most experienced director on the board, commencing their role in 2020. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.
Board Change • Apr 05High number of new and inexperienced directorsThere are 8 new directors who have joined the board in the last 3 years. The company's board is composed of: 8 new directors. No experienced directors. No highly experienced directors. Independent Chairman of the Board Francesco de Rubertis is the most experienced director on the board, commencing their role in 2020. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.
Seeking Alpha • Dec 23Checking In On Centessa PharmaceuticalsToday, we put Centessa Pharmaceuticals in the spotlight for the first time. Centessa has a unique business model, multiple potential shots on goal, is deep in Busted IPO territory and has picked up some recent insider buying. A full investment analysis follows in the paragraphs below.