Serina Therapeutics（SER）株式概要バイオテクノロジー企業であるセリナ・セラピューティクス社は、神経疾患と疼痛の治療薬を開発している。 詳細SER ファンダメンタル分析スノーフレーク・スコア評価1/6将来の成長0/6過去の実績0/6財務の健全性5/6配当金0/6リスク分析収益が 100 万ドル未満 ( $130K )過去1年間で株主の希薄化は大幅に進んだ 今後3年間の収益は年平均16.2%減少すると予測されている。 US市場と比較した過去 3 か月間の株価の変動+2 さらなるリスクすべてのリスクチェックを見るSER Community Fair Values Create NarrativeSee what others think this stock is worth. Follow their fair value or set your own to get alerts.NEW480,575 membersJoin community and earn perksGain real feedbackFrom our editorial team, personally. Not silence.Grow your followingReal investors. The kind who actually invest, not scroll past.Unlock free accessFree premium subscription for consistent and quality authors.Learn moreCreate NarrativeBLINRODA480,575 investors already sharing narrativesYour Fair ValueUS$Current PriceUS$2.00該当なし内在価値ディスカウントGrowth estimate overAnnual revenue growth rate5 Yearstime period%/yrDecreaseIncreasePastFuture-22m3m2016201920222025202620282031Revenue US$12.2Earnings US$2.2AdvancedSet Fair ValueView all narrativesSerina Therapeutics, Inc. 競合他社ABVC BioPharmaSymbol: NasdaqCM:ABVCMarket cap: US$27.3mBarinthus BiotherapeuticsSymbol: NasdaqCM:BRNSMarket cap: US$22.8mTScan TherapeuticsSymbol: NasdaqGM:TCRXMarket cap: US$49.4mAligos TherapeuticsSymbol: NasdaqCM:ALGSMarket cap: US$26.7m価格と性能株価の高値、安値、推移の概要Serina Therapeutics過去の株価現在の株価US$2.0052週高値US$7.9252週安値US$1.22ベータ0.0291ヶ月の変化4.17%3ヶ月変化10.07%1年変化-62.19%3年間の変化n/a5年間の変化n/aIPOからの変化-86.55%最新ニュースお知らせ • Jul 23Serina Therapeutics, Inc. Announces Appointment of Farrell Simon to Board of Directors and Board Committees, Effective July 22, 2026Serina Therapeutics, Inc. had announced the appointment of Farrell Simon, Pharm. D., to the Company's Board of Directors, effective July 22, 2026. Dr. Simon had also been appointed to serve as a member of the Audit Committee and Compensation Committee. Dr. Simon is a biotech, pharmaceutical and consumer health executive with expertise in commercial strategy, operations, and business development. He currently serves as Chief Commercial Officer at Trevi Therapeutics, Inc., where he leads commercial strategy, lifecycle management, and pre-commercial readiness planning. He also leads business development efforts for potential partnerships and M&A. During his tenure at Trevi, he helped engage Trevi's investor base and supported financings totaling more than $400 million from top-tier investors including Frazier, Vivo, Venrock, and Viking. Prior to Trevi, Dr. Simon spent a decade at Pfizer in a series of senior commercial and strategic leadership roles, including Biopharma Chief of Staff and global commercial leadership positions supporting major brands and pipeline assets. He holds a Doctor of Pharmacy degree and an MBA, with a concentration in Finance, from the University of Florida.お知らせ • Jul 09Serina Therapeutics, Inc. Completes Sentinel Dosing In Cohort 1 Of Phase 1b Registrational Trial Of SER-252 For Advanced Parkinson’s DiseaseSerina Therapeutics, Inc. announced the completion of sentinel dosing in Cohort 1 of its ongoing Phase 1b registrational clinical trial evaluating SER-252 in patients with advanced Parkinson’s disease. Following review of initial 72-hour safety and tolerability observations from the sentinel dosing group, the study’s independent Safety Monitoring Committee recommended that dosing continue in the remainder of Cohort 1. Additional patient dosing in Cohort 1 is now underway across sites in the United States and Australia. Serina previously guided that completion of enrollment and dosing in Cohort 1 was expected by the end of the third quarter of 2026. Based on current site activity and patient screening and dosing, the Company now expects to complete enrollment and dosing of Cohort 1 ahead of that timeline, subject to continued trial execution. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b registrational trial with single-ascending-dose and multiple-ascending-dose components in adults with Parkinson’s disease and motor fluctuations. The study is designed to evaluate the safety, tolerability and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation is overseen by a Safety Monitoring Committee, and the study is being conducted across sites in Australia and the United States, with plans to bring on sites in South Korea and Taiwan as the study advances through subsequent cohorts. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b trial with single-ascending-dose (five cohorts of eight; n=40) and multiple-ascending-dose components (up to three cohorts of sixteen; n=48) in adults with Parkinson’s disease and motor fluctuations. The registrational study is designed to evaluate safety, tolerability, and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation will be overseen by an independent Safety Monitoring Committee, and the study is being conducted across sites in the United States, Australia with plans to South Korea and Taiwan. Serina’s proprietary POZ technology is based on a synthetic, water-soluble, low viscosity polymer called poly (2-oxazoline). Serina’s POZ technology is engineered to provide greater control in drug loading and more precision in the rate of release of attached drugs delivered via subcutaneous injection. The therapeutic agents in Serina’s product candidates are typically well-understood and marketed drugs that are effective but are limited by pharmacokinetic profiles that can include toxicity, side effects and short half-life. Serina believes that by using POZ technology, drugs with narrow therapeutic windows can be designed to maintain more desirable and stable levels in the blood. Serina’s POZ platform delivery technology has potential for use across a broad range of payloads and indications. Serina intends to advance additional applications of the POZ platform via out-licensing, co-development, or other partnership arrangements, including the non-exclusive license agreement with Pfizer, Inc. to use Serina’s POZ polymer technology for use in lipid nanoparticle drug (LNP) delivery formulations. SER 252 is an investigational apomorphine therapy developed with Serina’s POZ platform and designed to provide continuous dopaminergic stimulation (CDS). CDS has been shown to reduce the severity of levodopa-related motor complications (dyskinesia) in Parkinson’s disease. Preclinical studies support the potential of SER 252 to provide CDS without skin reactions.New Risk • May 05New major risk - Shareholder dilutionThe company's shareholders have been substantially diluted in the past year. Increase in shares outstanding: 49% 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 Risks Share price has been highly volatile over the past 3 months (33% average weekly change). Negative equity (-US$37k). Earnings are forecast to decline by an average of 25% per year for the foreseeable future. Shareholders have been substantially diluted in the past year (49% increase in shares outstanding). Revenue is less than US$1m (US$130k revenue). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$34m net loss in 3 years). Market cap is less than US$100m (US$28.3m market cap).お知らせ • Apr 21Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026.お知らせ • Apr 08Serina Therapeutics, Inc Announces Novel Lipid Nanoparticles Built On POZ PlatformSerina Therapeutics, Inc. announced that Serina Therapeutics Chief Development Officer, Randall Moreadith, MD, PhD, will be presenting at the 5th LNP Formulation & Process Development Summit in Boston, MA. Entitled "Novel Lipid Nanoparticles Built Entirely on a POZ Platform", Dr. Moreadith will present data demonstrating the POZ-lipid in Serina’s platform failed to elicit an antibody response to the polymer in a vaccine format in the rat. The standard PEG-lipid in most LNP formulations elicits a prompt IgM and IgG response and has been shown to be associated with serious adverse events in some individuals. The Serina LNP Laboratory is also advancing an additional replacement strategy targeting ionizable lipids, another essential LNP component that has been implicated in safety concerns. Preliminary results from Serina’s studies of a novel polymer-lipid designed to bind a broad range of oligonucleotide payloads will also be featured in the presentation, underscoring the company’s commitment to improving both the safety and versatility of LNP-based therapeutics.Reported Earnings • Mar 27Full year 2025 earnings: EPS exceeds analyst expectationsFull year 2025 results: US$1.88 loss per share (further deteriorated from US$1.51 loss in FY 2024). Net loss: US$19.2m (loss widened 72% from FY 2024). Revenue is expected to decline by 86% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 20%.最新情報をもっと見るRecent updatesお知らせ • Jul 23Serina Therapeutics, Inc. Announces Appointment of Farrell Simon to Board of Directors and Board Committees, Effective July 22, 2026Serina Therapeutics, Inc. had announced the appointment of Farrell Simon, Pharm. D., to the Company's Board of Directors, effective July 22, 2026. Dr. Simon had also been appointed to serve as a member of the Audit Committee and Compensation Committee. Dr. Simon is a biotech, pharmaceutical and consumer health executive with expertise in commercial strategy, operations, and business development. He currently serves as Chief Commercial Officer at Trevi Therapeutics, Inc., where he leads commercial strategy, lifecycle management, and pre-commercial readiness planning. He also leads business development efforts for potential partnerships and M&A. During his tenure at Trevi, he helped engage Trevi's investor base and supported financings totaling more than $400 million from top-tier investors including Frazier, Vivo, Venrock, and Viking. Prior to Trevi, Dr. Simon spent a decade at Pfizer in a series of senior commercial and strategic leadership roles, including Biopharma Chief of Staff and global commercial leadership positions supporting major brands and pipeline assets. He holds a Doctor of Pharmacy degree and an MBA, with a concentration in Finance, from the University of Florida.お知らせ • Jul 09Serina Therapeutics, Inc. Completes Sentinel Dosing In Cohort 1 Of Phase 1b Registrational Trial Of SER-252 For Advanced Parkinson’s DiseaseSerina Therapeutics, Inc. announced the completion of sentinel dosing in Cohort 1 of its ongoing Phase 1b registrational clinical trial evaluating SER-252 in patients with advanced Parkinson’s disease. Following review of initial 72-hour safety and tolerability observations from the sentinel dosing group, the study’s independent Safety Monitoring Committee recommended that dosing continue in the remainder of Cohort 1. Additional patient dosing in Cohort 1 is now underway across sites in the United States and Australia. Serina previously guided that completion of enrollment and dosing in Cohort 1 was expected by the end of the third quarter of 2026. Based on current site activity and patient screening and dosing, the Company now expects to complete enrollment and dosing of Cohort 1 ahead of that timeline, subject to continued trial execution. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b registrational trial with single-ascending-dose and multiple-ascending-dose components in adults with Parkinson’s disease and motor fluctuations. The study is designed to evaluate the safety, tolerability and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation is overseen by a Safety Monitoring Committee, and the study is being conducted across sites in Australia and the United States, with plans to bring on sites in South Korea and Taiwan as the study advances through subsequent cohorts. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b trial with single-ascending-dose (five cohorts of eight; n=40) and multiple-ascending-dose components (up to three cohorts of sixteen; n=48) in adults with Parkinson’s disease and motor fluctuations. The registrational study is designed to evaluate safety, tolerability, and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation will be overseen by an independent Safety Monitoring Committee, and the study is being conducted across sites in the United States, Australia with plans to South Korea and Taiwan. Serina’s proprietary POZ technology is based on a synthetic, water-soluble, low viscosity polymer called poly (2-oxazoline). Serina’s POZ technology is engineered to provide greater control in drug loading and more precision in the rate of release of attached drugs delivered via subcutaneous injection. The therapeutic agents in Serina’s product candidates are typically well-understood and marketed drugs that are effective but are limited by pharmacokinetic profiles that can include toxicity, side effects and short half-life. Serina believes that by using POZ technology, drugs with narrow therapeutic windows can be designed to maintain more desirable and stable levels in the blood. Serina’s POZ platform delivery technology has potential for use across a broad range of payloads and indications. Serina intends to advance additional applications of the POZ platform via out-licensing, co-development, or other partnership arrangements, including the non-exclusive license agreement with Pfizer, Inc. to use Serina’s POZ polymer technology for use in lipid nanoparticle drug (LNP) delivery formulations. SER 252 is an investigational apomorphine therapy developed with Serina’s POZ platform and designed to provide continuous dopaminergic stimulation (CDS). CDS has been shown to reduce the severity of levodopa-related motor complications (dyskinesia) in Parkinson’s disease. Preclinical studies support the potential of SER 252 to provide CDS without skin reactions.New Risk • May 05New major risk - Shareholder dilutionThe company's shareholders have been substantially diluted in the past year. Increase in shares outstanding: 49% 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 Risks Share price has been highly volatile over the past 3 months (33% average weekly change). Negative equity (-US$37k). Earnings are forecast to decline by an average of 25% per year for the foreseeable future. Shareholders have been substantially diluted in the past year (49% increase in shares outstanding). Revenue is less than US$1m (US$130k revenue). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$34m net loss in 3 years). Market cap is less than US$100m (US$28.3m market cap).お知らせ • Apr 21Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026.お知らせ • Apr 08Serina Therapeutics, Inc Announces Novel Lipid Nanoparticles Built On POZ PlatformSerina Therapeutics, Inc. announced that Serina Therapeutics Chief Development Officer, Randall Moreadith, MD, PhD, will be presenting at the 5th LNP Formulation & Process Development Summit in Boston, MA. Entitled "Novel Lipid Nanoparticles Built Entirely on a POZ Platform", Dr. Moreadith will present data demonstrating the POZ-lipid in Serina’s platform failed to elicit an antibody response to the polymer in a vaccine format in the rat. The standard PEG-lipid in most LNP formulations elicits a prompt IgM and IgG response and has been shown to be associated with serious adverse events in some individuals. The Serina LNP Laboratory is also advancing an additional replacement strategy targeting ionizable lipids, another essential LNP component that has been implicated in safety concerns. Preliminary results from Serina’s studies of a novel polymer-lipid designed to bind a broad range of oligonucleotide payloads will also be featured in the presentation, underscoring the company’s commitment to improving both the safety and versatility of LNP-based therapeutics.Reported Earnings • Mar 27Full year 2025 earnings: EPS exceeds analyst expectationsFull year 2025 results: US$1.88 loss per share (further deteriorated from US$1.51 loss in FY 2024). Net loss: US$19.2m (loss widened 72% from FY 2024). Revenue is expected to decline by 86% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 20%.Recent Insider Transactions Derivative • Mar 22Chief Development Officer exercised options and sold US$95k worth of stockOn the 19th of March, Randall Moreadith exercised 39k options at a strike price of around US$0.06 and sold these shares for an average price of US$2.50 per share. This trade did not impact their existing holding. Since June 2025, Randall has not owned shares directly. Company insiders have collectively sold US$1.1m more than they bought, via options and on-market transactions in the last 12 months.お知らせ • Mar 19+ 1 more updateSerina Therapeutics, Inc. announced that it expects to receive $30 million in fundingSerina Therapeutics, Inc. announces that it has entered into definitive agreements for the private placement of common stock and pre-funded warrants for gross proceeds of $15 million and A second funding tranche of up to an additional gross proceeds of $15million for aggregate proceeds of $30million on March 18, 2026. This first tranche is expected to close on March 20, 2026. Second Tranche is anticipated to close on or before April 30, 2026. The transaction is led by Greg Bailey, M.D., a current Board Director who will assume the role of Co-Chairman of the Board of Directors. Under the terms of the agreements, Serina is selling shares of common stock at a purchase price of $2.25 per share and pre-funded warrants to purchase common stock at a purchase price equal to the Per Share Purchase Price minus the pre-funded warrant exercise price of $0.0001, with each common share or pre-funded warrant accompanied by a warrant to purchase one-half share of common stock at an exercise price of $5.00 per share. The securities described above are being offered in a private placement under Section 4(a)(2) of the Securities Act of 1933, as amended, and/or Regulation D.お知らせ • Feb 20Serina Therapeutics, Inc. Announces First Patient Enrolled in Phase 1b Registrational Trial of Ser-252 for Advanced Parkinson's DiseaseSerina Therapeutics, Inc. announced that the first patient has been enrolled in the Company's Phase 1b registrational trial evaluating SER-252 in patients with advanced Parkinson's disease. The Phase 1b registrational study is designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of SER-252 in patients with Advanced Parkinson's disease whose symptoms are inadequately controlled by current standard-of-care therapies. The Company plans to provide further updates on the trial as patient enrollment progresses.お知らせ • Jan 29Serina Therapeutics, Inc. Announces FDA Clearance of IND Application for Ser-252 for the Treatment of Advanced Parkinson's DiseaseSerina Therapeutics, Inc. announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for SER-252, an investigational therapy for advanced Parkinson's disease. The IND clearance allows Serina to proceed with regulatory and site-level activities to support initiation of a planned Phase 1b registrational clinical study evaluating SER-252 in patients with advanced Parkinson's disease.Recent Insider Transactions Derivative • Jan 21Chief Development Officer notifies of intention to sell stockRandall Moreadith intends to sell 91k shares in the next 90 days after lodging an Intent To Sell Form on the 20th of January. If the sale is conducted around the recent share price of US$3.07, it would amount to US$279k. Since March 2025, Randall has not owned shares directly (This sale likely refers to shares that have not yet been received). Company insiders have collectively sold US$930k more than they bought, via options and on-market transactions in the last 12 months.お知らせ • Jan 16Serina Therapeutics, Inc. Receives Non-Compliance Notice from Nasdaq Regarding Minimum Stockholders’ Equity RequirementsOn January 9, 2026, Serina Therapeutics, Inc. (the “Company”) received a notification (the “Letter”) from The NYSE American LLC (the “NYSE American”) stating that the Company is not in compliance with the minimum stockholders’ equity requirements of Sections 1003(a)(i), 1003(a)(ii), and 1003(a)(iii) of the NYSE American Company Guide (the “Company Guide”) requiring stockholders’ equity of (i) $2.0 million or more if the Company has reported losses from continuing operations and/or net losses in two of its three most recent fiscal years, (ii) $4.0 million or more if the Company has reported losses from continuing operations and/or net losses in three of the four most recent fiscal years and (iii) $6.0 million or more if the Company has reported losses from continuing operations and/or net losses in its five most recent fiscal years, respectively. As of September 30, 2025, the Company had stockholders’ equity of $1.6 million and has had losses in three of its four most recent fiscal years ended December 31, 2024. The Company is now subject to the procedures and requirements of Section 1009 of the Company Guide. The Company has until February 8, 2026 to submit a plan (the “Plan”) of actions it has taken or will take to regain compliance with the continued listing standards by July 9, 2027, which is eighteen months from receipt of the Letter (“Cure Period”). The Company intends to submit the Plan to regain compliance with NYSE American listing standards, however there can be no assurance that the Company will be able to achieve compliance with such standards within the Cure Period. If the NYSE American accepts the Plan, the Company will be able to continue its listing during the Cure Period and will be subject to periodic reviews including quarterly monitoring for compliance with the Plan until it has regained compliance. If the Plan is not accepted by the NYSE American, the Letter states that delisting proceedings will commence. The Company may appeal a staff delisting determination in accordance with Section 1010 and Part 12 of the Company Guide. The notice has no immediate impact on the listing of the Company’s shares of common stock, which will continue to be listed and traded on the NYSE American, subject to the Company’s compliance with the other listing requirements of the NYSE American. The notice does not affect the Company’s ongoing business operations or its reporting requirements with the Securities and Exchange Commission.New Risk • Jan 03New 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 11% 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 Risks Less than 1 year of cash runway based on free cash flow trend (-US$17m free cash flow). Earnings are forecast to decline by an average of 19% per year for the foreseeable future. Revenue is less than US$1m (US$116k revenue). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$38m net loss in 3 years). Share price has been volatile over the past 3 months (11% average weekly change). Market cap is less than US$100m (US$20.4m market cap).お知らせ • Dec 12Serina Therapeutics, Inc. Announces Appointment of Joshua Thomas as Head of ChemistrySerina Therapeutics, Inc. announced the appointment of Joshua Thomas, Ph.D., as Head of Chemistry. He will oversee internal and external chemistry efforts to optimize POZ-based candidates, supporting efficient translation from discovery through development. Prior to joining Serina, Dr. Thomas served in progressive scientific leadership roles at Mersana Therapeutics, where during his 13 years he played a pivotal part in building out their discovery chemistry capabilities. Notably, he played a key role in the development of a novel STING agonist ADC platform. He has led groundbreaking research programs in antibody drug conjugate (ADC) technologies, focused on developing innovative “warhead” and linker elements that have advanced multiple platforms into clinical trials. His expertise encompasses both developing cytotoxic payloads with novel mechanisms of action and designing complex bioconjugation systems for targeted cancer therapies. Dr. Thomas earned his Ph.D. in Medicinal Chemistry from the University of Florida and completed postdoctoral training in cancer research at the National Cancer Institute. He holds a B.S. in Chemistry from Wingate University. Over his career, he has contributed to multiple development candidates, patents, and publications spanning small molecules and conjugate-based modalities. His experience integrating cutting-edge chemistry with translational objectives aligns with Serina’s strategy of building a sustainable discovery and development engine for polymer-enabled therapeutics.お知らせ • Dec 11Serina Therapeutics, Inc. Submits Complete Response to FDA Clinical Hold Letter for Ser-252 ProgramSerina Therapeutics, Inc. announced that it has submitted a complete response to the U.S. Food and Drug Administration's clinical hold letter for SER-252, the Company's lead program for advanced Parkinson's disease. As previously disclosed, the FDA placed the Company's Investigational New Drug application for SER-252 on clinical hold pending additional information related to a commonly used formulation excipient. On November 25, 2025, the FDA issued a formal full clinical hold letter specifying the information required to permit initiation of the planned Phase 1b registrational study, SER-252-1b. The issues identified by the FDA do not relate to the apomorphine active drug substance, its mechanism of action, the use of the enFuse device (Enable Injections) or the broader 505(b)(2) NDA development pathway previously discussed with the Agency. Initiation of the SAD phase of the SER-252-1b trial is anticipated to begin in First Quarter 2026. While dosing cannot begin until the clinical hold is lifted, Serina continues site start-up and regulatory activities in Australia and other regions as part of the global registrational program. In Australia, early interactions with investigators and the Parkinson's community have helped build strong support for the trial design and its potential to address unmet needs in advanced disease. The Company now expects first-patient-in ("FPI") in First Quarter 2026, subject to timely resolution of the clinical hold and customary regulatory and ethics approvals.Reported Earnings • Nov 16Third quarter 2025 earnings released: US$0.44 loss per share (vs US$0.16 profit in 3Q 2024)Third quarter 2025 results: US$0.44 loss per share (down from US$0.16 profit in 3Q 2024). Net loss: US$4.59m (down 425% from profit in 3Q 2024). Revenue is expected to decline by 82% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 21%.お知らせ • Nov 03Serina Therapeutics, Inc. Provides Regulatory Update on Ser-252 ProgramSerina Therapeutics, Inc. announced that the U.S. Food and Drug Administration (FDA) has placed a clinical hold on the Company's Investigational New Drug (IND) application for SER-252, Serina's lead development program for advanced Parkinson's disease. The FDA has requested additional information related to a commonly used excipient in the formulation. The feedback does not relate to the active drug substance or its proposed mechanism of action. Serina intends to work expeditiously with the FDA to address the requests. Serina expects to receive the FDA's formal clinical-hold letter within 30 days and will provide an update once it has aligned with the FDA on next steps and timelines. In prior interactions, the FDA indicated support for Serina's development approach for SER-252 under a 505(b)(2) NDA pathway. Regulatory feedback of this kind is a normal and constructive part of responsible drug development. The team has full confidence as they work closely with the FDA to address its comments. Dose escalation will be overseen by a Safety Review Committee and the study will be conducted across sites in the U.S. and Australia. SER 252 is an investigational apomorphine therapy developed with Serina's POZ platform and designed to provide continuous dopaminergic stimulation (CDS) via a single or twice-weekly subcutaneous injection. CDS has been shown to reduce the severity of motor fluctuations (which includes levodopa-induced dyskinesia) and enable greater daily on time, with reduced off time, in advanced Parkinson's patients. SER-252 leverages strategic partner Enable Injections' enFuse™? wearable drug delivery platform to enhance patient comfort and convenience, providing CDS to patients via an easy-to-administer, long-acting subcutaneous injection. About the POZ Platform™? Serina's proprietary POZ technology is based on a synthetic, water soluble, low viscosity polymer called poly (2-oxazoline). Serina's POZ platform delivery technology has potential for use across a broad range of payloads and indications.Recent Insider Transactions Derivative • Oct 15Chief Development Officer notifies of intention to sell stockRandall Moreadith intends to sell 89k shares in the next 90 days after lodging an Intent To Sell Form on the 13th of October. If the sale is conducted around the recent share price of US$5.97, it would amount to US$530k. Since December 2024, Randall has not owned shares directly (This sale likely refers to shares that have not yet been received). Company insiders have collectively sold US$617k more than they bought, via options and on-market transactions in the last 12 months.お知らせ • Oct 08Serina Therapeutics Launches Enhanced Corporate Communications Platform to Strengthen Engagement with Patients, Clinicians, and InvestorsSerina Therapeutics, Inc. announced the launch of a comprehensive corporate communications platform designed to deliver timely, transparent updates to patients, clinicians, investors, and the broader scientific community. The new initiative expands Serina's direct channels of communication to provide stakeholders with clear, accessible information on the Company's programs, regulatory progress, and scientific advances. The platform will feature regular digital updates, educational resources, multimedia content, and expert commentary from company leadership and scientific advisors. As part of the initiative, Serina plans to provide: Program and clinical updates delivered through the Company's website and newsletters; Educational resources for physicians, patients, and scientists to better understand the potential of POZ-enabled therapeutics in improving therapeutic performance across multiple modalities; Multimedia content, including a new podcast series, to highlight perspectives from company leaders, investigators, and thought leaders in neuroscience and other therapeutic areas; Opportunities for engagement, including webinars and online forums to support dialogue with patient and professional communities. This platform is designed to complement Serina's ongoing clinical and regulatory activities, providing stakeholders with real-time access to relevant information as the Company advances its pipeline.お知らせ • Sep 11Serina Therapeutics, Inc. announced that it expects to receive $20 million in fundingSerina Therapeutics, Inc. announced that it has entered into an agreement to issue unsecured convertible note and warrants for gross proceeds of $20,000,000 on September 9, 2025. The transaction is led by Greg Bailey. The notes will be convertible into common share at conversion price of $5.18 per share. The notes accrue interest at the rate of 10%, payable quarterly after the first year. The notes will mature five year from initial funding. The warrant exercise price is of $5.44. Warrants expire upon the earlier of 60 days following achievement of phase 1b first patient dosing in Cohort 2 or September 30, 2026. The unsecured convertible notes will be issued in five tranches. The company will issue convertible notes for proceeds of $5,000,000 in its first tranche on or before October 1, 2025. The company will issue convertible notes for proceeds of $2,500,000 in its second tranche upon enrollment of phase 1b first patient on or after December 15, 2025. The company will issue convertible notes for proceeds of $2,500,000 in its third tranche upon enrollment of phase 1b second patient. The company will issue convertible notes for proceeds of $5,000,000 in its fourth tranche upon dosing of phase 1b last patient in Cohort 1 on or after March 15, 2026. The company will issue convertible notes for proceeds of $5,000,000 in its fifth tranche upon dosing of phase 1b first patient in Cohort 2 on or after April 30, 2026.Recent Insider Transactions Derivative • Aug 28Chief Development Officer exercised options and sold US$329k worth of stockOn the 26th of August, Randall Moreadith exercised 48k options at a strike price of around US$0.06 and sold these shares for an average price of US$6.95 per share. This trade did not impact their existing holding. Since December 2024, Randall has not owned shares directly. Company insiders have collectively sold US$461k more than they bought, via options and on-market transactions in the last 12 months.お知らせ • Aug 26Serina Therapeutics, Inc. Announces FDA Feedback Supports Registrational Trial Design of Ser-252 in Advanced Parkinson's Disease Under 505(b)(2) NDA PathwaySerina Therapeutics, Inc. announced that following a recent Type B meeting with the U.S. Food and Drug Administration (FDA), the FDA's written feedback supports advancing SER-252 (POZ-apomorphine) in a registrational clinical study program in advanced Parkinson's under the 505(b)(2) NDA pathway. In its discussions with the FDA, Serina outlined a program designed to leverage prior knowledge of apomorphine utilizing the company's POZ-enabled profile. Serina plans to include a pharmacokinetic (PK) bridging component to an approved apomorphine product, consistent with a 505(b)(2)NDA strategy. The FDA's feedback indicates that SER-252's initial study may be designed and conducted as a component of a registrational trial program, subject to standard clinical and nonclinical requirements and finalization of documentation at the time of IND submission. Serina plans to submit the U.S. IND application in Fourth Quarter 2025 incorporating the FDA's recommendations. In parallel, the company expects to begin dosing patients in Australia in Fourth Quarter 2025 as part of the global registrational program, with data from these patients expected to contribute to the overall data package for regulatory review and potential approval. Dose escalation will be overseen by a Safety Review Committee and the study will be conducted across sites in the U.S. and Australia. SER 252 is an investigational apomorphine therapy developed with Serina's POZ platform and designed to provide continuous dopaminergic stimulation (CDS) via a single or twice-weekly subcutaneous injection. CDS has been shown to reduce the severity of motor fluctuations (which includes levodopa-induced dyskinesia) and enable greater daily on time, with reduced off time, in advanced Parkinson's patients. SER-252 leverages strategic partner Enable Injections' enFuse™? wearable drug delivery platform to enhance patient comfort and convenience, providing CDS to patients via an easy-to-administer, long-acting subcutaneous injection.Reported Earnings • Aug 13Second quarter 2025 earnings released: US$0.65 loss per share (vs US$0.61 profit in 2Q 2024)Second quarter 2025 results: US$0.65 loss per share (down from US$0.61 profit in 2Q 2024). Net loss: US$6.45m (down 224% from profit in 2Q 2024). Revenue is expected to decline by 95% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 19%.お知らせ • Jul 29Serina Therapeutics Advances POZ-VMAT2i into Development for Tardive Dyskinesia (TD)Serina Therapeutics, Inc. announced the advancement of its novel product candidate, SER-270, a proprietary POZ-conjugated vesicular monoamine transporter 2 (VMAT2) inhibitor in development for the treatment of tardive dyskinesia (TD). SER-270, also referred to as POZ-VMAT2i, leverages Serina's proprietary POZ polymer technology to enable long-acting, once weekly subcutaneous administration, offering a potentially transformative alternative to existing oral VMAT2 inhibitors. The candidate is designed to meet the needs of underserved TD patients who struggle with daily medication adherence, including those already managed with long-acting injectable (LAI) antipsychotics. Addressing Significant Unmet Needs in TD: A Large and Under-Treated Market: TD is a disabling and often stigmatizing movement disorder caused by long-term exposure to antipsychotic medications. It predominantly affects those with chronic psychiatric conditions such as schizophrenia and bipolar disorder who may have difficulty adhering to complex daily medication regimens. While oral VMAT2 inhibitors are the only approved class for TD, uptake remains modest due to underdiagnosis, low disease awareness among clinicians, and the challenges of ensuring daily medication adherence in complex, high-risk populations. It is estimated that fewer than 30% of U.S. TD patients are diagnosed, and less than half of those receive pharmacologic treatment. Despite these challenges, the U.S. TD market exceeded $3.7 billion in sales in 2024, driven by increased recognition and broader reimbursement. Analysts project the market to grow to $5.4 billion by 2030, underscoring the significant opportunity for differentiated therapies that address adherence, access, and administration barriers.POZ-VMAT2i is uniquely positioned to address these barriers by offering: Once-weekly, long-acting injectable administration, critical for patients non-compliant with daily oral medications, including those currently managed with long-acting injectability (LAI) antipsychotic inhibitors. Improved access for institutionalized patients, where daily oral therapy poses logistical challenges for nursing and care staff. A non-oral solution for patients with dysphagia (chewing/swallowing difficulties), a common complication among elderly and neurologically impaired individuals. Serina also plans to explore development of POZ-VMAT2 i for chorea associated with Huntington's disease, a neurodegenerative disorder marked by progressive movement impairment and often, serious swallowing difficulties. A weekly injectable therapy may offer meaningful advantages over current oral options for this population and their caregivers.Recent Insider Transactions Derivative • Jul 03Chief Development Officer notifies of intention to sell stockRandall Moreadith intends to sell 100k shares in the next 90 days after lodging an Intent To Sell Form on the 30th of June. If the sale is conducted around the recent share price of US$5.78, it would amount to US$576k. Since December 2024, Randall has not owned shares directly (This sale likely refers to shares that have not yet been received). Company insiders have collectively bought US$373k more than they sold, via options and on-market transactions, in the last 12 months.お知らせ • Jul 02Serina Therapeutics, Inc., Annual General Meeting, Nov 07, 2025Serina Therapeutics, Inc., Annual General Meeting, Nov 07, 2025.Reported Earnings • May 10First quarter 2025 earnings released: US$0.49 loss per share (vs US$5.38 loss in 1Q 2024)First quarter 2025 results: US$0.49 loss per share (improved from US$5.38 loss in 1Q 2024). Net loss: US$4.81m (loss narrowed 68% from 1Q 2024).お知らせ • Apr 28Serina Therapeutics, Inc. has filed a Follow-on Equity Offering in the amount of $13.2705 million.Serina Therapeutics, Inc. has filed a Follow-on Equity Offering in the amount of $13.2705 million. Security Name: Common Stock Security Type: Common Stock Transaction Features: At the Market Offeringお知らせ • Apr 09Serina Therapeutics, Inc. announced that it has received $4.999995 million in fundingSerina Therapeutics, Inc. announced a private placement and issued 965,250 shares of convertible preferred stock at an issue price of $5.18 per share for gross proceeds of $4,999,995 on April 7, 2025. The company received financing from strategic shareholders.Reported Earnings • Mar 25Full year 2024 earnings released: US$1.51 loss per share (vs US$2.30 profit in FY 2023)Full year 2024 results: US$1.51 loss per share (down from US$2.30 profit in FY 2023). Net loss: US$11.1m (down 311% from profit in FY 2023). Revenue is expected to decline by 86% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 20%.New Risk • Mar 12New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 31% 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 Negative equity (-US$14m). Earnings are forecast to decline by an average of 31% per year for the foreseeable future. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$33m net loss in 3 years). Share price has been volatile over the past 3 months (13% average weekly change). Revenue is less than US$5m (US$3.2m revenue). Market cap is less than US$100m (US$45.9m market cap).お知らせ • Feb 13Serina Therapeutics Announces Board ChangesSerina Therapeutics, Inc. announced the appointment of Jay Venkatesan, MD, MBA, to its Board of Directors. Dr. Venkatesan brings deep expertise in biotechnology investment, company building, and strategic growth, having successfully led and advised multiple biopharma companies through pivotal stages of development, including high-profile mergers and acquisitions. Dr. Venkatesan most recently served as Chairman, President, and CEO of Angion Biomedica until its merger with Elicio Therapeutics in 2023. He currently serves as a Board Director at Elicio Therapeutics. Previously, he was President and Board Director of Alpine Immune Sciences, which he co-founded as a Managing Partner of Alpine BioVentures. Dr. Venkatesan has a distinguished career spanning investment and operational leadership roles. Before Alpine, he founded and managed Ayer Capital, a global healthcare investment fund. Earlier in his career, he was a director at Brookside Capital, a division of Bain Capital, where he co-managed healthcare investments. He also held roles as a venture investor with Patricof & Co. Ventures (now Apax Partners) and as a consultant at McKinsey & Co.Dr. Venkatesan holds an M.D. from the University of Pennsylvania School of Medicine and an M.B.A. from the Wharton School of the University of Pennsylvania. He earned his B.A. from Williams College. Serina’s co-founder, Dr. Milton Harris, will assume the role of Director Emeritus and will serve as Chair of the company’s Scientific Advisory Board (SAB). Dr. Harris has played an instrumental role in the development of Serina’s POZ Platform, providing leadership and scientific expertise that have shaped the company’s pipeline and clinical development. In his new role, he will provide continued guidance to Serina’s research and development efforts.お知らせ • Feb 04Serina Therapeutics, Inc. announced that it has received $10 million in fundingOn February 3, 2025, Serina Therapeutics, Inc closed the transaction. The company issued 500,000 shares at an issue price of $10 per share for the gross proceeds of $5,000,000 in first tranche.お知らせ • Jan 15Serina Therapeutics, Inc. Appoints Karen J. Wilson to its Board of DirectorsSerina Therapeutics, Inc. announced the appointment of Karen J. Wilson to the Board of Directors. Ms. Wilson brings over three decades of leadership experiences in the life sciences sector. She currently serves as a board director for Connect Biopharma Holdings Limited, Elicio Therapeutics, Inc. and LAVA Therapeutics N.V. Previously, she held the position of Senior Vice President of Finance at Jazz Pharmaceuticals plc, where she also served as Principal Accounting Officer and Vice President of Finance. Prior to joining the Jazz Pharmaceuticals organization in February 2011, she held senior finance roles at PDL BioPharma, ViroLogic, and Novare Surgical Systems and was a consultant and auditor for Deloitte & Touche LLP. Ms. Wilson is a Certified Public Accountant and received a B.S. in Business from the University of California, Berkeley. Serina also announced the departure of Steven Mintz from its Board of Directors.お知らせ • Dec 27JuvVentures (UK) Limited acquired UniverXome Bioengineering, Inc. from Serina Therapeutics, Inc. (NYSEAM:SER) for $11.2 million.JuvVentures (UK) Limited acquired UniverXome Bioengineering, Inc. from Serina Therapeutics, Inc. (NYSEAM:SER) for $11.2 million on December 23, 2024. The aggregate purchase price for the Shares shall be $10. As consideration for the purchase of UniverXome, Juvenescence assumed approximately $11.2 million of secured debt owed by UniverXome to Juvenescence in addition to a nominal cash payment. On December 23, 2024 , the Special Committee approved the execution and delivery by the Company of the Stock Purchase Agreement and the related transactions, including for purposes of the Company’s Related Person Transaction Policy. Jacqueline Mercier of Goodwin Procter LLP acted as legal advisor for JuvVentures Limited. Scott Ludwig of Bradley Arant Boult Cummings LLP acted as legal advisor for Serina Therapeutics, Inc. JuvVentures (UK) Limited completed the acquisition of UniverXome Bioengineering, Inc. from Serina Therapeutics, Inc. (NYSEAM:SER) on December 23, 2024.Reported Earnings • Nov 14Third quarter 2024 earnings released: EPS: US$0.16 (vs US$0.78 in 3Q 2023)Third quarter 2024 results: EPS: US$0.16 (down from US$0.78 in 3Q 2023). Revenue: US$14.0k (down 53% from 3Q 2023). Net income: US$1.41m (down 20% from 3Q 2023).お知らせ • Nov 04Serina Therapeutics, Inc., Annual General Meeting, Dec 13, 2024Serina Therapeutics, Inc., Annual General Meeting, Dec 13, 2024.Recent Insider Transactions • Sep 23Director recently bought US$88k worth of stockOn the 19th of September, Gregory Bailey bought around 14k shares on-market at roughly US$6.13 per share. This transaction amounted to 30% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger purchase worth US$140k. Insiders have collectively bought US$770k more in shares than they have sold in the last 12 months.Recent Insider Transactions • Aug 20Director recently bought US$59k worth of stockOn the 15th of August, Steven Mintz bought around 9k shares on-market at roughly US$6.59 per share. This transaction amounted to 38% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger purchase worth US$121k. Insiders have collectively bought US$488k more in shares than they have sold in the last 12 months.お知らせ • Aug 16+ 1 more updateSerina Therapeutics, Inc. Announces CFO ChangesOn August 15, 2024, the Board of Directors of Serina Therapeutics, Inc. appointed Gregory S. Curhan as the Company’s Chief Financial Officer in a non-employee consultant role, effective August 16, 2024. Mr. Curhan, age 62, has been a partner at FLG Partners, a Silicon Valley chief financial officer services firm, since January 2020, and since 2020 Mr. Curhan has also served as the CFO of Curevo Vaccines. From June 2020 until June 2023, Mr. Curhan also served as the Chief Financial Officer of Angion Biomedica Corp. Prior to joining FLG Partners, Mr. Curhan was Chief Financial Officer and Senior Vice President Corporate Development of Providence Medical Technology, December 2016 until January 2020. Prior to that, Mr. Curhan was a Business Development Officer at Brighton Jones, a financial planning company, from December 2012 to December 2016. Mr. Curhan has a B.A. in Economics from Dartmouth College. On August 12, 2024, the Company informed Andrea Park, the Company’s Interim Chief Financial Officer, that her employment with the Company will end effective August 15, 2024.Reported Earnings • Aug 11Second quarter 2024 earnings released: EPS: US$0.61 (vs US$0.37 in 2Q 2023)Second quarter 2024 results: EPS: US$0.61 (up from US$0.37 in 2Q 2023). Revenue: US$51.0k (up US$44.0k from 2Q 2023). Net income: US$5.20m (up US$4.40m from 2Q 2023).お知らせ • Jul 19Serina Therapeutics, Inc. Announces the Appointment of Dr. Srini Tenjarla as the New Senior Vice President of CMC (Chemistry, Manufacturing, and Controls) and FormulationSerina Therapeutics, Inc. announced the appointment of Dr. Srini Tenjarla as the new Senior Vice President of CMC (Chemistry, Manufacturing, and Controls) and Formulation. Dr. Tenjarla brings over 20 years of extensive experience in drug development to Serina. Dr. Tenjarla joins Serina Therapeutics from Takeda Pharmaceuticals, where he served as Vice President and Head of Drug Product Development and Process Chemistry Development/Outsourcing in Pharmaceutical Sciences. In this role, he provided technical and strategic leadership to global teams, overseeing phase-appropriate development from Phase 1 through product validation and PAI readiness. Prior to his tenure at Takeda, Dr. Tenjarla held several leadership roles at Shire Pharmaceuticals, culminating in his position as Vice President of Pharmaceutical Sciences. Dr. Tenjarla has a proven track record in advancing programs through clinical phases to NDA/BLA submission and approval. Throughout his career, Dr. Tenjarla has demonstrated expertise in formulation development across multiple modalities, including solid oral, injectables, controlled release, and ophthalmic formulations. He has led numerous global cross-functional teams and collaborated with CDMOs in Europe, the USA, China, India, and Japan. His contributions include setting up Preferred Vendor Networks and working closely with device and quality groups for combination product programs. Dr. Tenjarla holds a Ph.D. in Pharmaceutical Sciences from the University of Houston and a Bachelor of Science in Pharmacy from Andhra University. He is a recognized subject matter expert in formulation, with extensive experience managing programs, formulation, drug substance, analytical, and regulatory interactions.Recent Insider Transactions • Jun 28Director recently bought US$71k worth of stockOn the 25th of June, Steven Mintz bought around 8k shares on-market at roughly US$9.33 per share. This transaction amounted to 48% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger purchase worth US$121k. Insiders have collectively bought US$384k more in shares than they have sold in the last 12 months.New Risk • May 27New major risk - Negative shareholders equityThe company has negative equity. Total equity: -US$4.3m This is considered a major risk. Being in negative equity means that the company's liabilities exceed its assets, meaning it owes more to creditors than it has in owned assets. While this doesn't mean the company is about to collapse, in the long-term, this is unsustainable. The company may have issues meeting financial obligations, is at risk of becoming insolvent and may have difficulty raising capital, especially more debt, if needed. Currently, the following risks have been identified for the company: Major Risk Negative equity (-US$4.3m). Minor Risks Share price has been volatile over the past 3 months (15% average weekly change). Revenue is less than US$5m (US$3.1m revenue). Market cap is less than US$100m (US$82.8m market cap).Recent Insider Transactions • May 24Director recently bought US$121k worth of stockOn the 21st of May, Steven Mintz bought around 12k shares on-market at roughly US$9.76 per share. This transaction increased Steven's direct individual holding by 4x at the time of the trade. This was the largest purchase by an insider in the last 3 months. Insiders have collectively bought US$135k more in shares than they have sold in the last 12 months.Valuation Update With 7 Day Price Move • May 20Investor sentiment improves as stock rises 20%After last week's 20% share price gain to US$10.00, the stock trades at a trailing P/E ratio of 16x. Average trailing P/E is 24x in the Biotechs industry in the US.Valuation Update With 7 Day Price Move • Apr 23Investor sentiment deteriorates as stock falls 16%After last week's 16% share price decline to US$9.81, the stock trades at a trailing P/E ratio of 15.7x. Average trailing P/E is 20x in the Biotechs industry in the US.お知らせ • Apr 18Serina Therapeutics, Inc. Appoints Simba Gill as Executive ChairmanSerina Therapeutics, Inc. announced the appointment of Dr. Simba Gill as Executive Chairman. Serina’s proprietary POZ PlatformTM aims to develop and improve therapeutics across multiple modalities including small molecules, RNA-based therapeutics and antibody-based drug conjugates (ADCs). Simba brings to Serina a wealth of biotech and pharma experience in building companies and transformative platforms as well as developing products, having served in key roles at Maxygen, Systemix, Boehringer Mannheim and Celltech. He earned his MBA at INSEAD and received his Ph.D. from King’s College, London. Dr. Gill will play a pivotal role in guiding Serina through its next phase of growth and development, leveraging his expertise to drive strategic expansion initiatives.Reported Earnings • Apr 07Full year 2023 earnings released: EPS: US$2.30 (vs US$1.25 loss in FY 2022)Full year 2023 results: EPS: US$2.30 (up from US$1.25 loss in FY 2022). Net income: US$5.27m (up US$7.95m from FY 2022).Board Change • Mar 28No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 6 non-independent directors. was the last director to join the board, commencing their role in . The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.株主還元SERUS BiotechsUS 市場7D-3.4%-0.5%1.0%1Y-62.2%31.0%19.1%株主還元を見る業界別リターン: SER過去 1 年間で31 % の収益を上げたUS Biotechs業界を下回りました。リターン対市場: SERは、過去 1 年間で19.1 % のリターンを上げたUS市場を下回りました。価格変動Is SER's price volatile compared to industry and market?SER volatilitySER Average Weekly Movement11.4%Biotechs Industry Average Movement10.0%Market Average Movement7.2%10% most volatile stocks in US Market16.3%10% least volatile stocks in US Market3.2%安定した株価: SERの株価は、 US市場と比較して過去 3 か月間で変動しています。時間の経過による変動: SERの 週次ボラティリティ は過去 1 年間で19%から11%に減少しましたが、依然としてUS株の 75% よりも高くなっています。会社概要設立従業員CEO（最高経営責任者ウェブサイト200616Steve Ledgerserinatherapeutics.comバイオテクノロジー企業のセリナ・セラピューティクス社は、神経疾患や疼痛の治療薬を開発している。 同社の主力候補製品は、進行性パーキンソン病の治療を目的としたPOZ結合体であるSER 252（POZ-アポモルフィン）であり、現在第1相臨床試験が進行中である。また、脂質ナノ粒子に含まれるPEG-脂質の非免疫原性代替品であるPOZ-脂質も開発している。 また、同社は、初期のパーキンソン病およびむずむず脚症候群の治療を目的としたロチゴチンとPOZの複合体であるSER 214も開発しており、これは第1a相臨床試験を完了している。 さらに、感染症治療用のリポソームを介したリボ核酸（RNA）ワクチンにおけるPOZ技術の開発も進めている。同社は、SER-252の開発活動を支援するため、Gannet BioChem社と提携契約を締結している。Serina Therapeutics, Inc.は2006年に設立され、アラバマ州ハンツビルに本社を置いている。もっと見るSerina Therapeutics, Inc. 基礎のまとめSerina Therapeutics の収益と売上を時価総額と比較するとどうか。SER 基礎統計学時価総額US$30.59m収益（TTM）-US$21.56m売上高(TTM)US$130.00k230.7xP/Sレシオ-1.4xPER（株価収益率SER は割高か？公正価値と評価分析を参照収益と収入最新の決算報告書（TTM）に基づく主な収益性統計SER 損益計算書（TTM）収益US$130.00k売上原価US$13.40m売上総利益-US$13.27mその他の費用US$8.29m収益-US$21.56m直近の収益報告Mar 31, 2026次回決算日該当なし一株当たり利益（EPS）-1.44グロス・マージン-10,210.00%純利益率-16,583.08%有利子負債／自己資本比率17.1%SER の長期的なパフォーマンスは？過去の実績と比較を見るView Valuation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2026/07/31 14:33終値2026/07/31 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この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、レポートの活用方法に関するガイドやYouTubeのチュートリアルも用意しています。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Serina Therapeutics, Inc. 2 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。2 アナリスト機関Thomas ShraderBTIGJustin WalshJonesTrading Institutional Services, LLC
お知らせ • Jul 23Serina Therapeutics, Inc. Announces Appointment of Farrell Simon to Board of Directors and Board Committees, Effective July 22, 2026Serina Therapeutics, Inc. had announced the appointment of Farrell Simon, Pharm. D., to the Company's Board of Directors, effective July 22, 2026. Dr. Simon had also been appointed to serve as a member of the Audit Committee and Compensation Committee. Dr. Simon is a biotech, pharmaceutical and consumer health executive with expertise in commercial strategy, operations, and business development. He currently serves as Chief Commercial Officer at Trevi Therapeutics, Inc., where he leads commercial strategy, lifecycle management, and pre-commercial readiness planning. He also leads business development efforts for potential partnerships and M&A. During his tenure at Trevi, he helped engage Trevi's investor base and supported financings totaling more than $400 million from top-tier investors including Frazier, Vivo, Venrock, and Viking. Prior to Trevi, Dr. Simon spent a decade at Pfizer in a series of senior commercial and strategic leadership roles, including Biopharma Chief of Staff and global commercial leadership positions supporting major brands and pipeline assets. He holds a Doctor of Pharmacy degree and an MBA, with a concentration in Finance, from the University of Florida.
お知らせ • Jul 09Serina Therapeutics, Inc. Completes Sentinel Dosing In Cohort 1 Of Phase 1b Registrational Trial Of SER-252 For Advanced Parkinson’s DiseaseSerina Therapeutics, Inc. announced the completion of sentinel dosing in Cohort 1 of its ongoing Phase 1b registrational clinical trial evaluating SER-252 in patients with advanced Parkinson’s disease. Following review of initial 72-hour safety and tolerability observations from the sentinel dosing group, the study’s independent Safety Monitoring Committee recommended that dosing continue in the remainder of Cohort 1. Additional patient dosing in Cohort 1 is now underway across sites in the United States and Australia. Serina previously guided that completion of enrollment and dosing in Cohort 1 was expected by the end of the third quarter of 2026. Based on current site activity and patient screening and dosing, the Company now expects to complete enrollment and dosing of Cohort 1 ahead of that timeline, subject to continued trial execution. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b registrational trial with single-ascending-dose and multiple-ascending-dose components in adults with Parkinson’s disease and motor fluctuations. The study is designed to evaluate the safety, tolerability and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation is overseen by a Safety Monitoring Committee, and the study is being conducted across sites in Australia and the United States, with plans to bring on sites in South Korea and Taiwan as the study advances through subsequent cohorts. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b trial with single-ascending-dose (five cohorts of eight; n=40) and multiple-ascending-dose components (up to three cohorts of sixteen; n=48) in adults with Parkinson’s disease and motor fluctuations. The registrational study is designed to evaluate safety, tolerability, and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation will be overseen by an independent Safety Monitoring Committee, and the study is being conducted across sites in the United States, Australia with plans to South Korea and Taiwan. Serina’s proprietary POZ technology is based on a synthetic, water-soluble, low viscosity polymer called poly (2-oxazoline). Serina’s POZ technology is engineered to provide greater control in drug loading and more precision in the rate of release of attached drugs delivered via subcutaneous injection. The therapeutic agents in Serina’s product candidates are typically well-understood and marketed drugs that are effective but are limited by pharmacokinetic profiles that can include toxicity, side effects and short half-life. Serina believes that by using POZ technology, drugs with narrow therapeutic windows can be designed to maintain more desirable and stable levels in the blood. Serina’s POZ platform delivery technology has potential for use across a broad range of payloads and indications. Serina intends to advance additional applications of the POZ platform via out-licensing, co-development, or other partnership arrangements, including the non-exclusive license agreement with Pfizer, Inc. to use Serina’s POZ polymer technology for use in lipid nanoparticle drug (LNP) delivery formulations. SER 252 is an investigational apomorphine therapy developed with Serina’s POZ platform and designed to provide continuous dopaminergic stimulation (CDS). CDS has been shown to reduce the severity of levodopa-related motor complications (dyskinesia) in Parkinson’s disease. Preclinical studies support the potential of SER 252 to provide CDS without skin reactions.
New Risk • May 05New major risk - Shareholder dilutionThe company's shareholders have been substantially diluted in the past year. Increase in shares outstanding: 49% 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 Risks Share price has been highly volatile over the past 3 months (33% average weekly change). Negative equity (-US$37k). Earnings are forecast to decline by an average of 25% per year for the foreseeable future. Shareholders have been substantially diluted in the past year (49% increase in shares outstanding). Revenue is less than US$1m (US$130k revenue). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$34m net loss in 3 years). Market cap is less than US$100m (US$28.3m market cap).
お知らせ • Apr 21Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026.
お知らせ • Apr 08Serina Therapeutics, Inc Announces Novel Lipid Nanoparticles Built On POZ PlatformSerina Therapeutics, Inc. announced that Serina Therapeutics Chief Development Officer, Randall Moreadith, MD, PhD, will be presenting at the 5th LNP Formulation & Process Development Summit in Boston, MA. Entitled "Novel Lipid Nanoparticles Built Entirely on a POZ Platform", Dr. Moreadith will present data demonstrating the POZ-lipid in Serina’s platform failed to elicit an antibody response to the polymer in a vaccine format in the rat. The standard PEG-lipid in most LNP formulations elicits a prompt IgM and IgG response and has been shown to be associated with serious adverse events in some individuals. The Serina LNP Laboratory is also advancing an additional replacement strategy targeting ionizable lipids, another essential LNP component that has been implicated in safety concerns. Preliminary results from Serina’s studies of a novel polymer-lipid designed to bind a broad range of oligonucleotide payloads will also be featured in the presentation, underscoring the company’s commitment to improving both the safety and versatility of LNP-based therapeutics.
Reported Earnings • Mar 27Full year 2025 earnings: EPS exceeds analyst expectationsFull year 2025 results: US$1.88 loss per share (further deteriorated from US$1.51 loss in FY 2024). Net loss: US$19.2m (loss widened 72% from FY 2024). Revenue is expected to decline by 86% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 20%.
お知らせ • Jul 23Serina Therapeutics, Inc. Announces Appointment of Farrell Simon to Board of Directors and Board Committees, Effective July 22, 2026Serina Therapeutics, Inc. had announced the appointment of Farrell Simon, Pharm. D., to the Company's Board of Directors, effective July 22, 2026. Dr. Simon had also been appointed to serve as a member of the Audit Committee and Compensation Committee. Dr. Simon is a biotech, pharmaceutical and consumer health executive with expertise in commercial strategy, operations, and business development. He currently serves as Chief Commercial Officer at Trevi Therapeutics, Inc., where he leads commercial strategy, lifecycle management, and pre-commercial readiness planning. He also leads business development efforts for potential partnerships and M&A. During his tenure at Trevi, he helped engage Trevi's investor base and supported financings totaling more than $400 million from top-tier investors including Frazier, Vivo, Venrock, and Viking. Prior to Trevi, Dr. Simon spent a decade at Pfizer in a series of senior commercial and strategic leadership roles, including Biopharma Chief of Staff and global commercial leadership positions supporting major brands and pipeline assets. He holds a Doctor of Pharmacy degree and an MBA, with a concentration in Finance, from the University of Florida.
お知らせ • Jul 09Serina Therapeutics, Inc. Completes Sentinel Dosing In Cohort 1 Of Phase 1b Registrational Trial Of SER-252 For Advanced Parkinson’s DiseaseSerina Therapeutics, Inc. announced the completion of sentinel dosing in Cohort 1 of its ongoing Phase 1b registrational clinical trial evaluating SER-252 in patients with advanced Parkinson’s disease. Following review of initial 72-hour safety and tolerability observations from the sentinel dosing group, the study’s independent Safety Monitoring Committee recommended that dosing continue in the remainder of Cohort 1. Additional patient dosing in Cohort 1 is now underway across sites in the United States and Australia. Serina previously guided that completion of enrollment and dosing in Cohort 1 was expected by the end of the third quarter of 2026. Based on current site activity and patient screening and dosing, the Company now expects to complete enrollment and dosing of Cohort 1 ahead of that timeline, subject to continued trial execution. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b registrational trial with single-ascending-dose and multiple-ascending-dose components in adults with Parkinson’s disease and motor fluctuations. The study is designed to evaluate the safety, tolerability and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation is overseen by a Safety Monitoring Committee, and the study is being conducted across sites in Australia and the United States, with plans to bring on sites in South Korea and Taiwan as the study advances through subsequent cohorts. The SER-252-1b study is a randomized, double-blind, placebo-controlled Phase 1b trial with single-ascending-dose (five cohorts of eight; n=40) and multiple-ascending-dose components (up to three cohorts of sixteen; n=48) in adults with Parkinson’s disease and motor fluctuations. The registrational study is designed to evaluate safety, tolerability, and pharmacokinetics of subcutaneous SER-252 versus placebo, with exploratory efficacy measures that include MDS-UPDRS motor scores and structured motor-state assessments. Dose escalation will be overseen by an independent Safety Monitoring Committee, and the study is being conducted across sites in the United States, Australia with plans to South Korea and Taiwan. Serina’s proprietary POZ technology is based on a synthetic, water-soluble, low viscosity polymer called poly (2-oxazoline). Serina’s POZ technology is engineered to provide greater control in drug loading and more precision in the rate of release of attached drugs delivered via subcutaneous injection. The therapeutic agents in Serina’s product candidates are typically well-understood and marketed drugs that are effective but are limited by pharmacokinetic profiles that can include toxicity, side effects and short half-life. Serina believes that by using POZ technology, drugs with narrow therapeutic windows can be designed to maintain more desirable and stable levels in the blood. Serina’s POZ platform delivery technology has potential for use across a broad range of payloads and indications. Serina intends to advance additional applications of the POZ platform via out-licensing, co-development, or other partnership arrangements, including the non-exclusive license agreement with Pfizer, Inc. to use Serina’s POZ polymer technology for use in lipid nanoparticle drug (LNP) delivery formulations. SER 252 is an investigational apomorphine therapy developed with Serina’s POZ platform and designed to provide continuous dopaminergic stimulation (CDS). CDS has been shown to reduce the severity of levodopa-related motor complications (dyskinesia) in Parkinson’s disease. Preclinical studies support the potential of SER 252 to provide CDS without skin reactions.
New Risk • May 05New major risk - Shareholder dilutionThe company's shareholders have been substantially diluted in the past year. Increase in shares outstanding: 49% 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 Risks Share price has been highly volatile over the past 3 months (33% average weekly change). Negative equity (-US$37k). Earnings are forecast to decline by an average of 25% per year for the foreseeable future. Shareholders have been substantially diluted in the past year (49% increase in shares outstanding). Revenue is less than US$1m (US$130k revenue). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$34m net loss in 3 years). Market cap is less than US$100m (US$28.3m market cap).
お知らせ • Apr 21Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026Serina Therapeutics, Inc., Annual General Meeting, Jun 17, 2026.
お知らせ • Apr 08Serina Therapeutics, Inc Announces Novel Lipid Nanoparticles Built On POZ PlatformSerina Therapeutics, Inc. announced that Serina Therapeutics Chief Development Officer, Randall Moreadith, MD, PhD, will be presenting at the 5th LNP Formulation & Process Development Summit in Boston, MA. Entitled "Novel Lipid Nanoparticles Built Entirely on a POZ Platform", Dr. Moreadith will present data demonstrating the POZ-lipid in Serina’s platform failed to elicit an antibody response to the polymer in a vaccine format in the rat. The standard PEG-lipid in most LNP formulations elicits a prompt IgM and IgG response and has been shown to be associated with serious adverse events in some individuals. The Serina LNP Laboratory is also advancing an additional replacement strategy targeting ionizable lipids, another essential LNP component that has been implicated in safety concerns. Preliminary results from Serina’s studies of a novel polymer-lipid designed to bind a broad range of oligonucleotide payloads will also be featured in the presentation, underscoring the company’s commitment to improving both the safety and versatility of LNP-based therapeutics.
Reported Earnings • Mar 27Full year 2025 earnings: EPS exceeds analyst expectationsFull year 2025 results: US$1.88 loss per share (further deteriorated from US$1.51 loss in FY 2024). Net loss: US$19.2m (loss widened 72% from FY 2024). Revenue is expected to decline by 86% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 20%.
Recent Insider Transactions Derivative • Mar 22Chief Development Officer exercised options and sold US$95k worth of stockOn the 19th of March, Randall Moreadith exercised 39k options at a strike price of around US$0.06 and sold these shares for an average price of US$2.50 per share. This trade did not impact their existing holding. Since June 2025, Randall has not owned shares directly. Company insiders have collectively sold US$1.1m more than they bought, via options and on-market transactions in the last 12 months.
お知らせ • Mar 19+ 1 more updateSerina Therapeutics, Inc. announced that it expects to receive $30 million in fundingSerina Therapeutics, Inc. announces that it has entered into definitive agreements for the private placement of common stock and pre-funded warrants for gross proceeds of $15 million and A second funding tranche of up to an additional gross proceeds of $15million for aggregate proceeds of $30million on March 18, 2026. This first tranche is expected to close on March 20, 2026. Second Tranche is anticipated to close on or before April 30, 2026. The transaction is led by Greg Bailey, M.D., a current Board Director who will assume the role of Co-Chairman of the Board of Directors. Under the terms of the agreements, Serina is selling shares of common stock at a purchase price of $2.25 per share and pre-funded warrants to purchase common stock at a purchase price equal to the Per Share Purchase Price minus the pre-funded warrant exercise price of $0.0001, with each common share or pre-funded warrant accompanied by a warrant to purchase one-half share of common stock at an exercise price of $5.00 per share. The securities described above are being offered in a private placement under Section 4(a)(2) of the Securities Act of 1933, as amended, and/or Regulation D.
お知らせ • Feb 20Serina Therapeutics, Inc. Announces First Patient Enrolled in Phase 1b Registrational Trial of Ser-252 for Advanced Parkinson's DiseaseSerina Therapeutics, Inc. announced that the first patient has been enrolled in the Company's Phase 1b registrational trial evaluating SER-252 in patients with advanced Parkinson's disease. The Phase 1b registrational study is designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of SER-252 in patients with Advanced Parkinson's disease whose symptoms are inadequately controlled by current standard-of-care therapies. The Company plans to provide further updates on the trial as patient enrollment progresses.
お知らせ • Jan 29Serina Therapeutics, Inc. Announces FDA Clearance of IND Application for Ser-252 for the Treatment of Advanced Parkinson's DiseaseSerina Therapeutics, Inc. announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for SER-252, an investigational therapy for advanced Parkinson's disease. The IND clearance allows Serina to proceed with regulatory and site-level activities to support initiation of a planned Phase 1b registrational clinical study evaluating SER-252 in patients with advanced Parkinson's disease.
Recent Insider Transactions Derivative • Jan 21Chief Development Officer notifies of intention to sell stockRandall Moreadith intends to sell 91k shares in the next 90 days after lodging an Intent To Sell Form on the 20th of January. If the sale is conducted around the recent share price of US$3.07, it would amount to US$279k. Since March 2025, Randall has not owned shares directly (This sale likely refers to shares that have not yet been received). Company insiders have collectively sold US$930k more than they bought, via options and on-market transactions in the last 12 months.
お知らせ • Jan 16Serina Therapeutics, Inc. Receives Non-Compliance Notice from Nasdaq Regarding Minimum Stockholders’ Equity RequirementsOn January 9, 2026, Serina Therapeutics, Inc. (the “Company”) received a notification (the “Letter”) from The NYSE American LLC (the “NYSE American”) stating that the Company is not in compliance with the minimum stockholders’ equity requirements of Sections 1003(a)(i), 1003(a)(ii), and 1003(a)(iii) of the NYSE American Company Guide (the “Company Guide”) requiring stockholders’ equity of (i) $2.0 million or more if the Company has reported losses from continuing operations and/or net losses in two of its three most recent fiscal years, (ii) $4.0 million or more if the Company has reported losses from continuing operations and/or net losses in three of the four most recent fiscal years and (iii) $6.0 million or more if the Company has reported losses from continuing operations and/or net losses in its five most recent fiscal years, respectively. As of September 30, 2025, the Company had stockholders’ equity of $1.6 million and has had losses in three of its four most recent fiscal years ended December 31, 2024. The Company is now subject to the procedures and requirements of Section 1009 of the Company Guide. The Company has until February 8, 2026 to submit a plan (the “Plan”) of actions it has taken or will take to regain compliance with the continued listing standards by July 9, 2027, which is eighteen months from receipt of the Letter (“Cure Period”). The Company intends to submit the Plan to regain compliance with NYSE American listing standards, however there can be no assurance that the Company will be able to achieve compliance with such standards within the Cure Period. If the NYSE American accepts the Plan, the Company will be able to continue its listing during the Cure Period and will be subject to periodic reviews including quarterly monitoring for compliance with the Plan until it has regained compliance. If the Plan is not accepted by the NYSE American, the Letter states that delisting proceedings will commence. The Company may appeal a staff delisting determination in accordance with Section 1010 and Part 12 of the Company Guide. The notice has no immediate impact on the listing of the Company’s shares of common stock, which will continue to be listed and traded on the NYSE American, subject to the Company’s compliance with the other listing requirements of the NYSE American. The notice does not affect the Company’s ongoing business operations or its reporting requirements with the Securities and Exchange Commission.
New Risk • Jan 03New 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 11% 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 Risks Less than 1 year of cash runway based on free cash flow trend (-US$17m free cash flow). Earnings are forecast to decline by an average of 19% per year for the foreseeable future. Revenue is less than US$1m (US$116k revenue). Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$38m net loss in 3 years). Share price has been volatile over the past 3 months (11% average weekly change). Market cap is less than US$100m (US$20.4m market cap).
お知らせ • Dec 12Serina Therapeutics, Inc. Announces Appointment of Joshua Thomas as Head of ChemistrySerina Therapeutics, Inc. announced the appointment of Joshua Thomas, Ph.D., as Head of Chemistry. He will oversee internal and external chemistry efforts to optimize POZ-based candidates, supporting efficient translation from discovery through development. Prior to joining Serina, Dr. Thomas served in progressive scientific leadership roles at Mersana Therapeutics, where during his 13 years he played a pivotal part in building out their discovery chemistry capabilities. Notably, he played a key role in the development of a novel STING agonist ADC platform. He has led groundbreaking research programs in antibody drug conjugate (ADC) technologies, focused on developing innovative “warhead” and linker elements that have advanced multiple platforms into clinical trials. His expertise encompasses both developing cytotoxic payloads with novel mechanisms of action and designing complex bioconjugation systems for targeted cancer therapies. Dr. Thomas earned his Ph.D. in Medicinal Chemistry from the University of Florida and completed postdoctoral training in cancer research at the National Cancer Institute. He holds a B.S. in Chemistry from Wingate University. Over his career, he has contributed to multiple development candidates, patents, and publications spanning small molecules and conjugate-based modalities. His experience integrating cutting-edge chemistry with translational objectives aligns with Serina’s strategy of building a sustainable discovery and development engine for polymer-enabled therapeutics.
お知らせ • Dec 11Serina Therapeutics, Inc. Submits Complete Response to FDA Clinical Hold Letter for Ser-252 ProgramSerina Therapeutics, Inc. announced that it has submitted a complete response to the U.S. Food and Drug Administration's clinical hold letter for SER-252, the Company's lead program for advanced Parkinson's disease. As previously disclosed, the FDA placed the Company's Investigational New Drug application for SER-252 on clinical hold pending additional information related to a commonly used formulation excipient. On November 25, 2025, the FDA issued a formal full clinical hold letter specifying the information required to permit initiation of the planned Phase 1b registrational study, SER-252-1b. The issues identified by the FDA do not relate to the apomorphine active drug substance, its mechanism of action, the use of the enFuse device (Enable Injections) or the broader 505(b)(2) NDA development pathway previously discussed with the Agency. Initiation of the SAD phase of the SER-252-1b trial is anticipated to begin in First Quarter 2026. While dosing cannot begin until the clinical hold is lifted, Serina continues site start-up and regulatory activities in Australia and other regions as part of the global registrational program. In Australia, early interactions with investigators and the Parkinson's community have helped build strong support for the trial design and its potential to address unmet needs in advanced disease. The Company now expects first-patient-in ("FPI") in First Quarter 2026, subject to timely resolution of the clinical hold and customary regulatory and ethics approvals.
Reported Earnings • Nov 16Third quarter 2025 earnings released: US$0.44 loss per share (vs US$0.16 profit in 3Q 2024)Third quarter 2025 results: US$0.44 loss per share (down from US$0.16 profit in 3Q 2024). Net loss: US$4.59m (down 425% from profit in 3Q 2024). Revenue is expected to decline by 82% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 21%.
お知らせ • Nov 03Serina Therapeutics, Inc. Provides Regulatory Update on Ser-252 ProgramSerina Therapeutics, Inc. announced that the U.S. Food and Drug Administration (FDA) has placed a clinical hold on the Company's Investigational New Drug (IND) application for SER-252, Serina's lead development program for advanced Parkinson's disease. The FDA has requested additional information related to a commonly used excipient in the formulation. The feedback does not relate to the active drug substance or its proposed mechanism of action. Serina intends to work expeditiously with the FDA to address the requests. Serina expects to receive the FDA's formal clinical-hold letter within 30 days and will provide an update once it has aligned with the FDA on next steps and timelines. In prior interactions, the FDA indicated support for Serina's development approach for SER-252 under a 505(b)(2) NDA pathway. Regulatory feedback of this kind is a normal and constructive part of responsible drug development. The team has full confidence as they work closely with the FDA to address its comments. Dose escalation will be overseen by a Safety Review Committee and the study will be conducted across sites in the U.S. and Australia. SER 252 is an investigational apomorphine therapy developed with Serina's POZ platform and designed to provide continuous dopaminergic stimulation (CDS) via a single or twice-weekly subcutaneous injection. CDS has been shown to reduce the severity of motor fluctuations (which includes levodopa-induced dyskinesia) and enable greater daily on time, with reduced off time, in advanced Parkinson's patients. SER-252 leverages strategic partner Enable Injections' enFuse™? wearable drug delivery platform to enhance patient comfort and convenience, providing CDS to patients via an easy-to-administer, long-acting subcutaneous injection. About the POZ Platform™? Serina's proprietary POZ technology is based on a synthetic, water soluble, low viscosity polymer called poly (2-oxazoline). Serina's POZ platform delivery technology has potential for use across a broad range of payloads and indications.
Recent Insider Transactions Derivative • Oct 15Chief Development Officer notifies of intention to sell stockRandall Moreadith intends to sell 89k shares in the next 90 days after lodging an Intent To Sell Form on the 13th of October. If the sale is conducted around the recent share price of US$5.97, it would amount to US$530k. Since December 2024, Randall has not owned shares directly (This sale likely refers to shares that have not yet been received). Company insiders have collectively sold US$617k more than they bought, via options and on-market transactions in the last 12 months.
お知らせ • Oct 08Serina Therapeutics Launches Enhanced Corporate Communications Platform to Strengthen Engagement with Patients, Clinicians, and InvestorsSerina Therapeutics, Inc. announced the launch of a comprehensive corporate communications platform designed to deliver timely, transparent updates to patients, clinicians, investors, and the broader scientific community. The new initiative expands Serina's direct channels of communication to provide stakeholders with clear, accessible information on the Company's programs, regulatory progress, and scientific advances. The platform will feature regular digital updates, educational resources, multimedia content, and expert commentary from company leadership and scientific advisors. As part of the initiative, Serina plans to provide: Program and clinical updates delivered through the Company's website and newsletters; Educational resources for physicians, patients, and scientists to better understand the potential of POZ-enabled therapeutics in improving therapeutic performance across multiple modalities; Multimedia content, including a new podcast series, to highlight perspectives from company leaders, investigators, and thought leaders in neuroscience and other therapeutic areas; Opportunities for engagement, including webinars and online forums to support dialogue with patient and professional communities. This platform is designed to complement Serina's ongoing clinical and regulatory activities, providing stakeholders with real-time access to relevant information as the Company advances its pipeline.
お知らせ • Sep 11Serina Therapeutics, Inc. announced that it expects to receive $20 million in fundingSerina Therapeutics, Inc. announced that it has entered into an agreement to issue unsecured convertible note and warrants for gross proceeds of $20,000,000 on September 9, 2025. The transaction is led by Greg Bailey. The notes will be convertible into common share at conversion price of $5.18 per share. The notes accrue interest at the rate of 10%, payable quarterly after the first year. The notes will mature five year from initial funding. The warrant exercise price is of $5.44. Warrants expire upon the earlier of 60 days following achievement of phase 1b first patient dosing in Cohort 2 or September 30, 2026. The unsecured convertible notes will be issued in five tranches. The company will issue convertible notes for proceeds of $5,000,000 in its first tranche on or before October 1, 2025. The company will issue convertible notes for proceeds of $2,500,000 in its second tranche upon enrollment of phase 1b first patient on or after December 15, 2025. The company will issue convertible notes for proceeds of $2,500,000 in its third tranche upon enrollment of phase 1b second patient. The company will issue convertible notes for proceeds of $5,000,000 in its fourth tranche upon dosing of phase 1b last patient in Cohort 1 on or after March 15, 2026. The company will issue convertible notes for proceeds of $5,000,000 in its fifth tranche upon dosing of phase 1b first patient in Cohort 2 on or after April 30, 2026.
Recent Insider Transactions Derivative • Aug 28Chief Development Officer exercised options and sold US$329k worth of stockOn the 26th of August, Randall Moreadith exercised 48k options at a strike price of around US$0.06 and sold these shares for an average price of US$6.95 per share. This trade did not impact their existing holding. Since December 2024, Randall has not owned shares directly. Company insiders have collectively sold US$461k more than they bought, via options and on-market transactions in the last 12 months.
お知らせ • Aug 26Serina Therapeutics, Inc. Announces FDA Feedback Supports Registrational Trial Design of Ser-252 in Advanced Parkinson's Disease Under 505(b)(2) NDA PathwaySerina Therapeutics, Inc. announced that following a recent Type B meeting with the U.S. Food and Drug Administration (FDA), the FDA's written feedback supports advancing SER-252 (POZ-apomorphine) in a registrational clinical study program in advanced Parkinson's under the 505(b)(2) NDA pathway. In its discussions with the FDA, Serina outlined a program designed to leverage prior knowledge of apomorphine utilizing the company's POZ-enabled profile. Serina plans to include a pharmacokinetic (PK) bridging component to an approved apomorphine product, consistent with a 505(b)(2)NDA strategy. The FDA's feedback indicates that SER-252's initial study may be designed and conducted as a component of a registrational trial program, subject to standard clinical and nonclinical requirements and finalization of documentation at the time of IND submission. Serina plans to submit the U.S. IND application in Fourth Quarter 2025 incorporating the FDA's recommendations. In parallel, the company expects to begin dosing patients in Australia in Fourth Quarter 2025 as part of the global registrational program, with data from these patients expected to contribute to the overall data package for regulatory review and potential approval. Dose escalation will be overseen by a Safety Review Committee and the study will be conducted across sites in the U.S. and Australia. SER 252 is an investigational apomorphine therapy developed with Serina's POZ platform and designed to provide continuous dopaminergic stimulation (CDS) via a single or twice-weekly subcutaneous injection. CDS has been shown to reduce the severity of motor fluctuations (which includes levodopa-induced dyskinesia) and enable greater daily on time, with reduced off time, in advanced Parkinson's patients. SER-252 leverages strategic partner Enable Injections' enFuse™? wearable drug delivery platform to enhance patient comfort and convenience, providing CDS to patients via an easy-to-administer, long-acting subcutaneous injection.
Reported Earnings • Aug 13Second quarter 2025 earnings released: US$0.65 loss per share (vs US$0.61 profit in 2Q 2024)Second quarter 2025 results: US$0.65 loss per share (down from US$0.61 profit in 2Q 2024). Net loss: US$6.45m (down 224% from profit in 2Q 2024). Revenue is expected to decline by 95% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 19%.
お知らせ • Jul 29Serina Therapeutics Advances POZ-VMAT2i into Development for Tardive Dyskinesia (TD)Serina Therapeutics, Inc. announced the advancement of its novel product candidate, SER-270, a proprietary POZ-conjugated vesicular monoamine transporter 2 (VMAT2) inhibitor in development for the treatment of tardive dyskinesia (TD). SER-270, also referred to as POZ-VMAT2i, leverages Serina's proprietary POZ polymer technology to enable long-acting, once weekly subcutaneous administration, offering a potentially transformative alternative to existing oral VMAT2 inhibitors. The candidate is designed to meet the needs of underserved TD patients who struggle with daily medication adherence, including those already managed with long-acting injectable (LAI) antipsychotics. Addressing Significant Unmet Needs in TD: A Large and Under-Treated Market: TD is a disabling and often stigmatizing movement disorder caused by long-term exposure to antipsychotic medications. It predominantly affects those with chronic psychiatric conditions such as schizophrenia and bipolar disorder who may have difficulty adhering to complex daily medication regimens. While oral VMAT2 inhibitors are the only approved class for TD, uptake remains modest due to underdiagnosis, low disease awareness among clinicians, and the challenges of ensuring daily medication adherence in complex, high-risk populations. It is estimated that fewer than 30% of U.S. TD patients are diagnosed, and less than half of those receive pharmacologic treatment. Despite these challenges, the U.S. TD market exceeded $3.7 billion in sales in 2024, driven by increased recognition and broader reimbursement. Analysts project the market to grow to $5.4 billion by 2030, underscoring the significant opportunity for differentiated therapies that address adherence, access, and administration barriers.POZ-VMAT2i is uniquely positioned to address these barriers by offering: Once-weekly, long-acting injectable administration, critical for patients non-compliant with daily oral medications, including those currently managed with long-acting injectability (LAI) antipsychotic inhibitors. Improved access for institutionalized patients, where daily oral therapy poses logistical challenges for nursing and care staff. A non-oral solution for patients with dysphagia (chewing/swallowing difficulties), a common complication among elderly and neurologically impaired individuals. Serina also plans to explore development of POZ-VMAT2 i for chorea associated with Huntington's disease, a neurodegenerative disorder marked by progressive movement impairment and often, serious swallowing difficulties. A weekly injectable therapy may offer meaningful advantages over current oral options for this population and their caregivers.
Recent Insider Transactions Derivative • Jul 03Chief Development Officer notifies of intention to sell stockRandall Moreadith intends to sell 100k shares in the next 90 days after lodging an Intent To Sell Form on the 30th of June. If the sale is conducted around the recent share price of US$5.78, it would amount to US$576k. Since December 2024, Randall has not owned shares directly (This sale likely refers to shares that have not yet been received). Company insiders have collectively bought US$373k more than they sold, via options and on-market transactions, in the last 12 months.
お知らせ • Jul 02Serina Therapeutics, Inc., Annual General Meeting, Nov 07, 2025Serina Therapeutics, Inc., Annual General Meeting, Nov 07, 2025.
Reported Earnings • May 10First quarter 2025 earnings released: US$0.49 loss per share (vs US$5.38 loss in 1Q 2024)First quarter 2025 results: US$0.49 loss per share (improved from US$5.38 loss in 1Q 2024). Net loss: US$4.81m (loss narrowed 68% from 1Q 2024).
お知らせ • Apr 28Serina Therapeutics, Inc. has filed a Follow-on Equity Offering in the amount of $13.2705 million.Serina Therapeutics, Inc. has filed a Follow-on Equity Offering in the amount of $13.2705 million. Security Name: Common Stock Security Type: Common Stock Transaction Features: At the Market Offering
お知らせ • Apr 09Serina Therapeutics, Inc. announced that it has received $4.999995 million in fundingSerina Therapeutics, Inc. announced a private placement and issued 965,250 shares of convertible preferred stock at an issue price of $5.18 per share for gross proceeds of $4,999,995 on April 7, 2025. The company received financing from strategic shareholders.
Reported Earnings • Mar 25Full year 2024 earnings released: US$1.51 loss per share (vs US$2.30 profit in FY 2023)Full year 2024 results: US$1.51 loss per share (down from US$2.30 profit in FY 2023). Net loss: US$11.1m (down 311% from profit in FY 2023). Revenue is expected to decline by 86% p.a. on average during the next 3 years, while revenues in the Biotechs industry in the US are expected to grow by 20%.
New Risk • Mar 12New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 31% 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 Negative equity (-US$14m). Earnings are forecast to decline by an average of 31% per year for the foreseeable future. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$33m net loss in 3 years). Share price has been volatile over the past 3 months (13% average weekly change). Revenue is less than US$5m (US$3.2m revenue). Market cap is less than US$100m (US$45.9m market cap).
お知らせ • Feb 13Serina Therapeutics Announces Board ChangesSerina Therapeutics, Inc. announced the appointment of Jay Venkatesan, MD, MBA, to its Board of Directors. Dr. Venkatesan brings deep expertise in biotechnology investment, company building, and strategic growth, having successfully led and advised multiple biopharma companies through pivotal stages of development, including high-profile mergers and acquisitions. Dr. Venkatesan most recently served as Chairman, President, and CEO of Angion Biomedica until its merger with Elicio Therapeutics in 2023. He currently serves as a Board Director at Elicio Therapeutics. Previously, he was President and Board Director of Alpine Immune Sciences, which he co-founded as a Managing Partner of Alpine BioVentures. Dr. Venkatesan has a distinguished career spanning investment and operational leadership roles. Before Alpine, he founded and managed Ayer Capital, a global healthcare investment fund. Earlier in his career, he was a director at Brookside Capital, a division of Bain Capital, where he co-managed healthcare investments. He also held roles as a venture investor with Patricof & Co. Ventures (now Apax Partners) and as a consultant at McKinsey & Co.Dr. Venkatesan holds an M.D. from the University of Pennsylvania School of Medicine and an M.B.A. from the Wharton School of the University of Pennsylvania. He earned his B.A. from Williams College. Serina’s co-founder, Dr. Milton Harris, will assume the role of Director Emeritus and will serve as Chair of the company’s Scientific Advisory Board (SAB). Dr. Harris has played an instrumental role in the development of Serina’s POZ Platform, providing leadership and scientific expertise that have shaped the company’s pipeline and clinical development. In his new role, he will provide continued guidance to Serina’s research and development efforts.
お知らせ • Feb 04Serina Therapeutics, Inc. announced that it has received $10 million in fundingOn February 3, 2025, Serina Therapeutics, Inc closed the transaction. The company issued 500,000 shares at an issue price of $10 per share for the gross proceeds of $5,000,000 in first tranche.
お知らせ • Jan 15Serina Therapeutics, Inc. Appoints Karen J. Wilson to its Board of DirectorsSerina Therapeutics, Inc. announced the appointment of Karen J. Wilson to the Board of Directors. Ms. Wilson brings over three decades of leadership experiences in the life sciences sector. She currently serves as a board director for Connect Biopharma Holdings Limited, Elicio Therapeutics, Inc. and LAVA Therapeutics N.V. Previously, she held the position of Senior Vice President of Finance at Jazz Pharmaceuticals plc, where she also served as Principal Accounting Officer and Vice President of Finance. Prior to joining the Jazz Pharmaceuticals organization in February 2011, she held senior finance roles at PDL BioPharma, ViroLogic, and Novare Surgical Systems and was a consultant and auditor for Deloitte & Touche LLP. Ms. Wilson is a Certified Public Accountant and received a B.S. in Business from the University of California, Berkeley. Serina also announced the departure of Steven Mintz from its Board of Directors.
お知らせ • Dec 27JuvVentures (UK) Limited acquired UniverXome Bioengineering, Inc. from Serina Therapeutics, Inc. (NYSEAM:SER) for $11.2 million.JuvVentures (UK) Limited acquired UniverXome Bioengineering, Inc. from Serina Therapeutics, Inc. (NYSEAM:SER) for $11.2 million on December 23, 2024. The aggregate purchase price for the Shares shall be $10. As consideration for the purchase of UniverXome, Juvenescence assumed approximately $11.2 million of secured debt owed by UniverXome to Juvenescence in addition to a nominal cash payment. On December 23, 2024 , the Special Committee approved the execution and delivery by the Company of the Stock Purchase Agreement and the related transactions, including for purposes of the Company’s Related Person Transaction Policy. Jacqueline Mercier of Goodwin Procter LLP acted as legal advisor for JuvVentures Limited. Scott Ludwig of Bradley Arant Boult Cummings LLP acted as legal advisor for Serina Therapeutics, Inc. JuvVentures (UK) Limited completed the acquisition of UniverXome Bioengineering, Inc. from Serina Therapeutics, Inc. (NYSEAM:SER) on December 23, 2024.
Reported Earnings • Nov 14Third quarter 2024 earnings released: EPS: US$0.16 (vs US$0.78 in 3Q 2023)Third quarter 2024 results: EPS: US$0.16 (down from US$0.78 in 3Q 2023). Revenue: US$14.0k (down 53% from 3Q 2023). Net income: US$1.41m (down 20% from 3Q 2023).
お知らせ • Nov 04Serina Therapeutics, Inc., Annual General Meeting, Dec 13, 2024Serina Therapeutics, Inc., Annual General Meeting, Dec 13, 2024.
Recent Insider Transactions • Sep 23Director recently bought US$88k worth of stockOn the 19th of September, Gregory Bailey bought around 14k shares on-market at roughly US$6.13 per share. This transaction amounted to 30% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger purchase worth US$140k. Insiders have collectively bought US$770k more in shares than they have sold in the last 12 months.
Recent Insider Transactions • Aug 20Director recently bought US$59k worth of stockOn the 15th of August, Steven Mintz bought around 9k shares on-market at roughly US$6.59 per share. This transaction amounted to 38% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger purchase worth US$121k. Insiders have collectively bought US$488k more in shares than they have sold in the last 12 months.
お知らせ • Aug 16+ 1 more updateSerina Therapeutics, Inc. Announces CFO ChangesOn August 15, 2024, the Board of Directors of Serina Therapeutics, Inc. appointed Gregory S. Curhan as the Company’s Chief Financial Officer in a non-employee consultant role, effective August 16, 2024. Mr. Curhan, age 62, has been a partner at FLG Partners, a Silicon Valley chief financial officer services firm, since January 2020, and since 2020 Mr. Curhan has also served as the CFO of Curevo Vaccines. From June 2020 until June 2023, Mr. Curhan also served as the Chief Financial Officer of Angion Biomedica Corp. Prior to joining FLG Partners, Mr. Curhan was Chief Financial Officer and Senior Vice President Corporate Development of Providence Medical Technology, December 2016 until January 2020. Prior to that, Mr. Curhan was a Business Development Officer at Brighton Jones, a financial planning company, from December 2012 to December 2016. Mr. Curhan has a B.A. in Economics from Dartmouth College. On August 12, 2024, the Company informed Andrea Park, the Company’s Interim Chief Financial Officer, that her employment with the Company will end effective August 15, 2024.
Reported Earnings • Aug 11Second quarter 2024 earnings released: EPS: US$0.61 (vs US$0.37 in 2Q 2023)Second quarter 2024 results: EPS: US$0.61 (up from US$0.37 in 2Q 2023). Revenue: US$51.0k (up US$44.0k from 2Q 2023). Net income: US$5.20m (up US$4.40m from 2Q 2023).
お知らせ • Jul 19Serina Therapeutics, Inc. Announces the Appointment of Dr. Srini Tenjarla as the New Senior Vice President of CMC (Chemistry, Manufacturing, and Controls) and FormulationSerina Therapeutics, Inc. announced the appointment of Dr. Srini Tenjarla as the new Senior Vice President of CMC (Chemistry, Manufacturing, and Controls) and Formulation. Dr. Tenjarla brings over 20 years of extensive experience in drug development to Serina. Dr. Tenjarla joins Serina Therapeutics from Takeda Pharmaceuticals, where he served as Vice President and Head of Drug Product Development and Process Chemistry Development/Outsourcing in Pharmaceutical Sciences. In this role, he provided technical and strategic leadership to global teams, overseeing phase-appropriate development from Phase 1 through product validation and PAI readiness. Prior to his tenure at Takeda, Dr. Tenjarla held several leadership roles at Shire Pharmaceuticals, culminating in his position as Vice President of Pharmaceutical Sciences. Dr. Tenjarla has a proven track record in advancing programs through clinical phases to NDA/BLA submission and approval. Throughout his career, Dr. Tenjarla has demonstrated expertise in formulation development across multiple modalities, including solid oral, injectables, controlled release, and ophthalmic formulations. He has led numerous global cross-functional teams and collaborated with CDMOs in Europe, the USA, China, India, and Japan. His contributions include setting up Preferred Vendor Networks and working closely with device and quality groups for combination product programs. Dr. Tenjarla holds a Ph.D. in Pharmaceutical Sciences from the University of Houston and a Bachelor of Science in Pharmacy from Andhra University. He is a recognized subject matter expert in formulation, with extensive experience managing programs, formulation, drug substance, analytical, and regulatory interactions.
Recent Insider Transactions • Jun 28Director recently bought US$71k worth of stockOn the 25th of June, Steven Mintz bought around 8k shares on-market at roughly US$9.33 per share. This transaction amounted to 48% of their direct individual holding at the time of the trade. In the last 3 months, they made an even bigger purchase worth US$121k. Insiders have collectively bought US$384k more in shares than they have sold in the last 12 months.
New Risk • May 27New major risk - Negative shareholders equityThe company has negative equity. Total equity: -US$4.3m This is considered a major risk. Being in negative equity means that the company's liabilities exceed its assets, meaning it owes more to creditors than it has in owned assets. While this doesn't mean the company is about to collapse, in the long-term, this is unsustainable. The company may have issues meeting financial obligations, is at risk of becoming insolvent and may have difficulty raising capital, especially more debt, if needed. Currently, the following risks have been identified for the company: Major Risk Negative equity (-US$4.3m). Minor Risks Share price has been volatile over the past 3 months (15% average weekly change). Revenue is less than US$5m (US$3.1m revenue). Market cap is less than US$100m (US$82.8m market cap).
Recent Insider Transactions • May 24Director recently bought US$121k worth of stockOn the 21st of May, Steven Mintz bought around 12k shares on-market at roughly US$9.76 per share. This transaction increased Steven's direct individual holding by 4x at the time of the trade. This was the largest purchase by an insider in the last 3 months. Insiders have collectively bought US$135k more in shares than they have sold in the last 12 months.
Valuation Update With 7 Day Price Move • May 20Investor sentiment improves as stock rises 20%After last week's 20% share price gain to US$10.00, the stock trades at a trailing P/E ratio of 16x. Average trailing P/E is 24x in the Biotechs industry in the US.
Valuation Update With 7 Day Price Move • Apr 23Investor sentiment deteriorates as stock falls 16%After last week's 16% share price decline to US$9.81, the stock trades at a trailing P/E ratio of 15.7x. Average trailing P/E is 20x in the Biotechs industry in the US.
お知らせ • Apr 18Serina Therapeutics, Inc. Appoints Simba Gill as Executive ChairmanSerina Therapeutics, Inc. announced the appointment of Dr. Simba Gill as Executive Chairman. Serina’s proprietary POZ PlatformTM aims to develop and improve therapeutics across multiple modalities including small molecules, RNA-based therapeutics and antibody-based drug conjugates (ADCs). Simba brings to Serina a wealth of biotech and pharma experience in building companies and transformative platforms as well as developing products, having served in key roles at Maxygen, Systemix, Boehringer Mannheim and Celltech. He earned his MBA at INSEAD and received his Ph.D. from King’s College, London. Dr. Gill will play a pivotal role in guiding Serina through its next phase of growth and development, leveraging his expertise to drive strategic expansion initiatives.
Reported Earnings • Apr 07Full year 2023 earnings released: EPS: US$2.30 (vs US$1.25 loss in FY 2022)Full year 2023 results: EPS: US$2.30 (up from US$1.25 loss in FY 2022). Net income: US$5.27m (up US$7.95m from FY 2022).
Board Change • Mar 28No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 6 non-independent directors. was the last director to join the board, commencing their role in . The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.
