Poolbeg Pharma（POLB）株式概要プールベッグ・ファーマPLCはバイオ医薬品会社として、英国でアンメット・メディカル・ニーズに対する医薬品の開発・商業化に取り組んでいる。 詳細POLB 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6/6配当金0/6リスク分析収益が 100 万ドル未満 ( £0 )過去1年間で株主の希薄化は大幅に進んだ 過去5年間で収益は年間12%減少しました。 意味のある時価総額がありません ( £60M )+2 さらなるリスクすべてのリスクチェックを見るPOLB Community Fair Values Create NarrativeSee what others think this stock is worth. Follow their fair value or set your own to get alerts.Your Fair ValueUK£Current PriceUK£0.085該当なし内在価値ディスカウントEst. Revenue$PastFuture-6m12016201920222025202620282031Revenue UK£1.0Earnings UK£0.1AdvancedSet Fair ValueView all narrativesPoolbeg Pharma PLC 競合他社Sareum HoldingsSymbol: AIM:SARMarket cap: UK£31.2mImmuPharmaSymbol: AIM:IMMMarket cap: UK£28.7mECO Animal Health GroupSymbol: AIM:EAHMarket cap: UK£63.0mAnimalcare GroupSymbol: AIM:ANCRMarket cap: UK£228.9m価格と性能株価の高値、安値、推移の概要Poolbeg Pharma過去の株価現在の株価UK£0.08552週高値UK£0.0952週安値UK£0.025ベータ1.771ヶ月の変化97.67%3ヶ月変化102.38%1年変化161.54%3年間の変化1.19%5年間の変化n/aIPOからの変化-20.93%最新ニュースお知らせ • May 11Poolbeg Pharma Receives Patent Grant For POLB 001 Cancer Immunotherapy-Induced CRS In CanadaPoolbeg Pharma had received formal notification of the grant for its POLB 001 cancer immunotherapy-induced Cytokine Release Syndrome patent application from the Canadian patent office. This represents the second national grant within Poolbeg's cancer immunotherapy-induced CRS patent family, following the grant by IP Australia announced in March 2026, and marks a further important milestone for the Company. This patent covers the use of any p38 MAPK inhibitor, including POLB 001, for the prevention of cancer immunotherapy-induced CRS, and is underpinned by proprietary data generated by Poolbeg. Poolbeg filed its initial oncology patent applications in the UK in January 2023 before entering the international Patent Cooperation Treaty system in January 2024. This new patent grant was accelerated through the Patent Prosecution Highway, which enables expedited examination in participating countries where a favourable ruling has already been secured in another participating jurisdiction. The Company's IP portfolio now spans both cancer immunotherapy-induced CRS and severe influenza across multiple jurisdictions, and Poolbeg continues to pursue protection in further territories. This grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's future value and appeal to potential partners.お知らせ • May 07Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026. Location: the offices of gravita at aldgate tower, 2 leman street, e1 8fa, london United Kingdomお知らせ • Apr 17Poolbeg Pharma plc Receives Clinical Trial Authorisation for Polb 001 Topical TrialPoolbeg Pharma announced that the UK Medicines and Healthcare products Regulatory Agency ("MHRA") has granted Clinical Trial Authorisation ("CTA") for the POLB 001 TOPICAL trial. With all required regulatory clearances now in place and site initiation visits scheduled, the trial remains on track to deliver interim data this summer. The Company also announces positive findings from new independent US focused payer research conducted by Acumetis Global indicates multi-billion-dollar peak sales potential in the United States. POLB 001 is being developed as a potential first approved preventative therapy for cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"). The TOPICAL trial will investigate POLB 001 in approximately 30 relapsed/refractory multiple myeloma patients receiving the approved bispecific antibody teclistamab, which has been supplied by Johnson & Johnson at no cost to Poolbeg. The study now spans six sites across the UK, with NHS Lothian in Edinburgh and the Royal Stoke University Hospital joining existing sites at the NHS Trusts at The Christie, The Royal Marsden, University College London Hospitals, and University Hospitals Birmingham. Site initiation visits are scheduled with patient screening set to commence shortly. Unlike many oncology studies, given that CRS is an acute condition which occurs within days or weeks of initiation of a bispecific antibody, the design of the TOPICAL trial will allow rapid read out. The research, which engaged current payers covering approximately 75 million lives across a mix of commercial insurance providers, Medicare and Medicaid, confirms the strong, clearly defined value proposition for POLB 001. In particular, findings underscore POLB 001's potential to play an important role in the management of CRS by reducing the significant hospital costs associated with the condition and enabling a meaningful shift in care away from specialist centres of excellence toward outpatient and community settings. The report also noted that CRS occurs in the majority of CAR T and bispecific antibody treatments, with no established diagnostic method currently available to predict either the likelihood or severity of CRS in individual patients. Dosing of bispecific antibodies must be withheld until CRS resolves, often delaying patients from achieving therapeutically effective dosing levels and prolonging hospitalisation, while those who experience high-grade CRS must permanently discontinue treatment, meaning that these patients can no longer receive the potentially life-saving treatment. The research reconfirmed the significant cost burden associated with managing CRS and that an effective preventative treatment would represent a compelling value proposition for healthcare systems. The findings highlight pricing levels that demonstrate POLB 001's multi-billion-dollar peak sales potential, providing increased confidence in the Company's anticipated market opportunity and further supports POLB 001's future value and appeal to potential partners.お知らせ • Nov 22Poolbeg Pharma plc Receives European Immunomodulator II Patent Application Covering POLB 001 for the Treatment of Severe InfluenzaPoolbeg Pharma announced that the European Patent Office has granted Poolbeg's European Immunomodulator II patent application covering POLB 001 for the treatment of severe influenza. POLB 001 is a potent and selective p38 MAP kinase inhibitor with strong potential across multiple disease areas, including the prevention and treatment of cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"), a potential market opportunity of over USD 10 billion, and the treatment of severe influenza. POLB 001 holds the potential to address significant unmet needs affecting patients and healthcare systems globally. Poolbeg is actively building a comprehensive, worldwide IP portfolio, with patents covering use of p38 MAPK inhibitors in patients with severe influenza and for the prevention and treatment of cancer Immunotherapy-induced CRS. This patent grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's value and appeal to potential partners.お知らせ • May 27Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025. Location: the offices of dac beachcroft llp, 25 walbrook, ec4n 8af, london United Kingdomお知らせ • May 23Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million.Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 6,000,000 Price\Range: £0.025最新情報をもっと見るRecent updatesお知らせ • May 11Poolbeg Pharma Receives Patent Grant For POLB 001 Cancer Immunotherapy-Induced CRS In CanadaPoolbeg Pharma had received formal notification of the grant for its POLB 001 cancer immunotherapy-induced Cytokine Release Syndrome patent application from the Canadian patent office. This represents the second national grant within Poolbeg's cancer immunotherapy-induced CRS patent family, following the grant by IP Australia announced in March 2026, and marks a further important milestone for the Company. This patent covers the use of any p38 MAPK inhibitor, including POLB 001, for the prevention of cancer immunotherapy-induced CRS, and is underpinned by proprietary data generated by Poolbeg. Poolbeg filed its initial oncology patent applications in the UK in January 2023 before entering the international Patent Cooperation Treaty system in January 2024. This new patent grant was accelerated through the Patent Prosecution Highway, which enables expedited examination in participating countries where a favourable ruling has already been secured in another participating jurisdiction. The Company's IP portfolio now spans both cancer immunotherapy-induced CRS and severe influenza across multiple jurisdictions, and Poolbeg continues to pursue protection in further territories. This grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's future value and appeal to potential partners.お知らせ • May 07Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026. Location: the offices of gravita at aldgate tower, 2 leman street, e1 8fa, london United Kingdomお知らせ • Apr 17Poolbeg Pharma plc Receives Clinical Trial Authorisation for Polb 001 Topical TrialPoolbeg Pharma announced that the UK Medicines and Healthcare products Regulatory Agency ("MHRA") has granted Clinical Trial Authorisation ("CTA") for the POLB 001 TOPICAL trial. With all required regulatory clearances now in place and site initiation visits scheduled, the trial remains on track to deliver interim data this summer. The Company also announces positive findings from new independent US focused payer research conducted by Acumetis Global indicates multi-billion-dollar peak sales potential in the United States. POLB 001 is being developed as a potential first approved preventative therapy for cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"). The TOPICAL trial will investigate POLB 001 in approximately 30 relapsed/refractory multiple myeloma patients receiving the approved bispecific antibody teclistamab, which has been supplied by Johnson & Johnson at no cost to Poolbeg. The study now spans six sites across the UK, with NHS Lothian in Edinburgh and the Royal Stoke University Hospital joining existing sites at the NHS Trusts at The Christie, The Royal Marsden, University College London Hospitals, and University Hospitals Birmingham. Site initiation visits are scheduled with patient screening set to commence shortly. Unlike many oncology studies, given that CRS is an acute condition which occurs within days or weeks of initiation of a bispecific antibody, the design of the TOPICAL trial will allow rapid read out. The research, which engaged current payers covering approximately 75 million lives across a mix of commercial insurance providers, Medicare and Medicaid, confirms the strong, clearly defined value proposition for POLB 001. In particular, findings underscore POLB 001's potential to play an important role in the management of CRS by reducing the significant hospital costs associated with the condition and enabling a meaningful shift in care away from specialist centres of excellence toward outpatient and community settings. The report also noted that CRS occurs in the majority of CAR T and bispecific antibody treatments, with no established diagnostic method currently available to predict either the likelihood or severity of CRS in individual patients. Dosing of bispecific antibodies must be withheld until CRS resolves, often delaying patients from achieving therapeutically effective dosing levels and prolonging hospitalisation, while those who experience high-grade CRS must permanently discontinue treatment, meaning that these patients can no longer receive the potentially life-saving treatment. The research reconfirmed the significant cost burden associated with managing CRS and that an effective preventative treatment would represent a compelling value proposition for healthcare systems. The findings highlight pricing levels that demonstrate POLB 001's multi-billion-dollar peak sales potential, providing increased confidence in the Company's anticipated market opportunity and further supports POLB 001's future value and appeal to potential partners.お知らせ • Nov 22Poolbeg Pharma plc Receives European Immunomodulator II Patent Application Covering POLB 001 for the Treatment of Severe InfluenzaPoolbeg Pharma announced that the European Patent Office has granted Poolbeg's European Immunomodulator II patent application covering POLB 001 for the treatment of severe influenza. POLB 001 is a potent and selective p38 MAP kinase inhibitor with strong potential across multiple disease areas, including the prevention and treatment of cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"), a potential market opportunity of over USD 10 billion, and the treatment of severe influenza. POLB 001 holds the potential to address significant unmet needs affecting patients and healthcare systems globally. Poolbeg is actively building a comprehensive, worldwide IP portfolio, with patents covering use of p38 MAPK inhibitors in patients with severe influenza and for the prevention and treatment of cancer Immunotherapy-induced CRS. This patent grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's value and appeal to potential partners.お知らせ • May 27Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025. Location: the offices of dac beachcroft llp, 25 walbrook, ec4n 8af, london United Kingdomお知らせ • May 23Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million.Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 6,000,000 Price\Range: £0.025お知らせ • May 20+ 1 more updatePoolbeg Pharma PLC has filed a Follow-on Equity Offering in the amount of £0.1 million.Poolbeg Pharma PLC has filed a Follow-on Equity Offering in the amount of £0.1 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 4,000,000 Price\Range: £0.025お知らせ • Mar 20Poolbeg Pharma plc Receives Korean Intellectual Property Office Grant in KoreaPoolbeg Pharma announced that the Korean Intellectual Property Office has notified the Company of its official decision to grant Poolbeg's Republic of Korea Immunomodulator II patent application providing protection to POLB 001 for the treatment of severe influenza to December 2038. POLB 001 is a potent and selective p38 MAP kinase inhibitor with strong potential across multiple disease areas, including the prevention and treatment of cancer immunotherapy-induced Cytokine Release Syndrome and severe influenza. POLB 001 holds the potential to address significant unmet needs affecting patients and healthcare systems globally. This patent grant further strengthens Poolbeg's IP portfolio. Poolbeg has a robust portfolio of patents in place covering p38 MAP kinase inhibitors for the treatment of severe influenza; and for POLB 001 for the prevention or treatment of hypercytokinemia. Additional patent applications have been filed to strengthen and complement Poolbeg's POLB 001 patent portfolio, particularly for cytokine release syndrome caused by cancer immunotherapies. Developing a strong intellectual property portfolio remains a key priority for Poolbeg, enhancing POLB 001's value and appeal to potential partners.お知らせ • Jan 03Poolbeg Expects to Become A Private Subsidiary of HOOKIPA and Apply for Cancellation of the Admission of Its Shares to Trading on AIMThe boards of directors (each a “Board”) of HOOKIPA Pharma Inc. (“HOOKIPA”) and Poolbeg Pharma plc (“Poolbeg”) are pleased to announce that they have entered into non-binding discussions for an all-share acquisition by HOOKIPA of Poolbeg (the “Potential Combination”) to create a strong clinical-stage biopharmaceutical company focused on developing and commercialising innovative medicines for critical unmet medical needs, with a special focus on next-generation immunotherapies for the treatment of cancer and other serious diseases (the “Combined Group”). HOOKIPA intends to remain as the listed entity for the Combined Group on the Nasdaq Capital Market and Poolbeg is expected to become a private subsidiary of HOOKIPA and apply for cancellation of the admission of its shares to trading on AIM.New Risk • Jan 02New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of British stocks, typically moving 13% a week. This is considered a major risk. Share price volatility 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. It may also indicate 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. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (13% average weekly change). Earnings are forecast to decline by an average of 13% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable next year (UK£6.0m net loss next year). Market cap is less than US$100m (UK£21.4m market cap, or US$26.4m).お知らせ • Jan 02Poolbeg Pharma PLC (AIM:POLB) entered into non-binding discussions to acquire HOOKIPA Pharma Inc. (NasdaqCM:HOOK) for $1.3 million in a reverse merger transaction.Poolbeg Pharma PLC (AIM:POLB) entered into non-binding discussions to acquire HOOKIPA Pharma Inc. (NasdaqCM:HOOK) for $1.3 million in a reverse merger transaction on January 2, 2025. The Boards believe that the Potential Combination would create a Nasdaq-listed Combined Group operated by a combined management team. Poolbeg shareholders will receive 0.03 HOOKIPA shares for each Poolbeg share held (the “ Exchange Ratio ”); based on the Exchange Ratio, the Potential Combination would have the effect (on the basis of the assumptions set out below and prior to the dilution resulting from the Fundraise (as defined below)) that Poolbeg shareholders prior to the completion of the Potential Combination are expected to receive, on a fully diluted basis, approximately 55% of the equity in the Combined Group (the “ Poolbeg Ownership Percentage ”) and HOOKIPA shareholders are expected to hold approximately 45% of the equity in the Combined Group (the “ HOOKIPA Ownership Percentage ”); HOOKIPA is expected to undertake a 100% primary private placement fundraise of up to approximately $30 million (the “ Fundraise ”) which will be funded into HOOKIPA immediately following the completion of the Potential Combination; a percentage of the potential value from certain of HOOKIPA’s programmes will be retained by holders of HOOKIPA shares as at a date to be determined ahead of completion of the Potential Combination (“ HOOKIPA Shareholders ”) via a contingent value right instrument (“ CVR ”); HOOKIPA intends to remain as the listed entity for the Combined Group on the Nasdaq Capital Market and Poolbeg is expected to become a private subsidiary of HOOKIPA and apply for cancellation of the admission of its shares to trading on AIM; and The Combined Group is expected to have operations in the European Union, the United Kingdom and the United States of America, and anticipates benefiting from a strong international leadership team comprised of the following individuals: Malte Peters: Chief Executive Officer, Cathal Friel: Poolbeg Co-Founder, Ian O’Connell: Chief Financial Officer, Poolbeg Co-Founder, Mark Winderlich: Chief Development Officer, David Allmond: Chief Business Officer and John McEvoy: Chief Legal Officer. Combination is subject to the satisfaction or waiver of a number of customary pre-conditions, including, amongst other things, the satisfactory completion of customary due diligence, finalisation of the terms of the transaction, Board approvals of binding terms and sufficient prior expressions of interest from participants in respect to the Fundraise. The Potential Combination would be subject to the approval of both HOOKIPA and Poolbeg shareholders and other conditions. Geoff Nash, Henrik Persson, Hamish Waller and Trisyia Jamaludin of Cavendish Capital Markets Ltd?acted as financial advisors to Poolbeg Pharma. Eugene Rozelman, David Coatenand and Harry Davies-Ball of Canaccord Genuity acted as financial advisors to Poolbeg Pharma. Chris Raff and Simon Chaudhuri from London office and Ashish Contractor from New York office of Moelis & Company acted as financial advisors to HOOKIPA.お知らせ • Nov 20Poolbeg Pharma plc Announces U.S. Patent Office Grants U.S. Immunomodulator I PatentPoolbeg Pharma announced that the U.S. Patent Office has notified the Company of its official decision to grant Poolbeg's US Immunomodulator I patent application. The claims cover POLB 001, and other p38 MAP kinase inhibitors, for the treatment of patients at risk of severe influenza after an immune response has been triggered, and for the treatment of hypercytokinemia (cytokine storm) characteristic of severe influenza. POLB 001 is a potent and selective Phase II-ready p38 MAP kinase inhibitor with strong potential across multiple disease areas. This patent grant further strengthens Poolbeg's robust Intellectual Property (IP) portfolio. The Company has patents in place covering p38 MAP kinase inhibitors for the treatment of severe influenza; and covering POLB 001 for the treatment of hypercyTokinemia. Further patent applications have been filed and have complementary coverage as the Company continues to expand its patent portfolio covering POLB 001 and the wider class of p38 MAP kinase inhibitors., particularly in respect of cytokine release syndrome induced by cancer immunotherapies. Building a robust IP portfolio is a key focus for Poolbeg to further enhance POLB 001's value and attractiveness to potential partners.分析記事 • Aug 20Companies Like Poolbeg Pharma (LON:POLB) Are In A Position To Invest In GrowthJust because a business does not make any money, does not mean that the stock will go down. For example, although...お知らせ • Jul 26Poolbeg Pharma Announces Voluntary Delist from OTCQB MarketPoolbeg Pharma PLC announced that it is voluntarily delisting its ordinary shares (‘Ordinary Shares’) from trading on the OTCQB Market due to low trading volume and the associated administrative requirements. The company's last day of trading on the OTCQB Market will be 29 July 2024. Poolbeg will retain its listing on the London Stock Exchange's AIM Market under its existing ticker ‘POLB’. The delisting from the OTCQB market will have no impact on Poolbeg's Ordinary Shares, which will continue to trade on the AIM Market. Poolbeg reaffirms its ambitions to be dual listed on a national securities exchange in the US, such as Nasdaq, subject to meeting their listing requirements at the appropriate time.お知らせ • May 11Poolbeg Pharma PLC, Annual General Meeting, Jun 13, 2024Poolbeg Pharma PLC, Annual General Meeting, Jun 13, 2024. Location: the offices of dac beachcroft llp, 25 walbrook, ec4n 8af, london United Kingdomお知らせ • May 03Poolbeg Pharma PLC Receives the Fully Granted Patent from the U.S. Patent Office for Its Immunomodulator II Patent ApplicationPoolbeg Pharma PLC announced that further to its announcement on 20 March 2024, the Company has received the fully granted patent from the U.S Patent Office for its Immunomodulator II patent application. The claims cover a class of drugs (including POLB 001) for treating hypercytokinaemia (cytokine storm) and for preventing hypercytokinaemia in a patient after an immune response has been triggered. This encompasses cytokine storm that is induced in any disease indication. This further strengthens the Company's robust intellectual property portfolio for POLB 001, thereby enhancing the value and attractiveness of POLB 001 to potential Pharma partners. Poolbeg is actively building a comprehensive and worldwide IP portfolio, with patents in place covering p38 MAP kinase inhibitors for the treatment of severe influenza; and covering POLB 001 for the treatment of hypercytokinaemia. Further patent applications have been filed and have complementary coverage as the Company continues to expand its patent portfolio covering POLB 001 and the wider class of p38 MAP kinase inhibitors, particularly in respect of the treatment of cytokine release syndrome following cancer immunotherapy.New Risk • Mar 31New minor risk - Financial data availabilityThe company's latest financial reports are more than 6 months old. Last reported fiscal period ended June 2023. This is considered a minor risk. If the company has not reported its earnings on time, it may have been delayed due to audit problems or it may be finding it difficult to reconcile its accounts. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 14% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Latest financial reports are more than 6 months old (reported June 2023 fiscal period end). Currently unprofitable and not forecast to become profitable next year (UK£5.8m net loss next year). Market cap is less than US$100m (UK£49.3m market cap, or US$62.1m).Recent Insider Transactions • Feb 22Executive Chairman of The Board recently bought UK£97k worth of stockOn the 19th of February, Cathal Friel bought around 830k shares on-market at roughly UK£0.12 per share. This transaction amounted to 2.3% of their direct individual holding at the time of the trade. This was the largest purchase by an insider in the last 3 months. This was Cathal's only on-market trade for the last 12 months.分析記事 • Feb 16We're Hopeful That Poolbeg Pharma (LON:POLB) Will Use Its Cash WiselyEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...お知らせ • Feb 15Poolbeg Pharma plc Appoints Cathal Friel as Executive ChairmanPoolbeg Pharma plc announced a change of Board role. Cathal Friel, Co-Founder, substantial shareholder, and currently Non-Executive Chairman of the company is assuming the role of Executive Chairman at the company effective immediately. Cathal brings valuable experience from his longstanding track record of value creation in a number of public companies, including as Co-Founder of Amryt Pharma plc. He was also the Executive Chairman and Co-Founder of hVIVO plc. Since then, Cathal and his team have transformed hVIVO into a fast growing, profitable company with revenues of over £56 million, a share price of c. 28 pence and a market capitalisation of c. £200 million. Cathal will continue to work closely with the Company's Chief Executive Officer, Jeremy Skillington and the now expanded leadership team, several of whom have recently joined from Amryt Pharma. Cathal will focus on it's strategic initiatives, leveraging his strong track record of value creation, including the company's growing focus upon rare and orphan diseases, whilst Jeremy will continue his successful leadership of the company's clinical programmes and business development efforts alongside David Allmond.お知らせ • Feb 12Independent Research Confirms >$10 Billion Market Opportunity for POLB 001 as A Preventative Therapy for Cancer Immunotherapy-Induced Cytokine Release Syndrome (CRS)Poolbeg Pharma PLC announced that independent research conducted on behalf of Poolbeg confirms a >$10 billion market opportunity for POLB 001 in Cancer Immunotherapy-Induced CRS as an orally delivered preventative therapy. Cancer immunotherapies have been approved in rare and orphan blood cancers and so the Company can see potential for POLB 001 in one or more of these cancer types. POLB 001 in cancer immunotherapy-induced CRS will be developed alongside Poolbeg's existing portfolio of assets including its influenza programme; its AI drug discovery programmes; and oral delivery of GLP-1 for obesity and other metabolic diseases. Rare and orphan diseases represent a significant value creation opportunity for the Company and its shareholders as they are underserved and there remains a substantial opportunity for innovative medicines to treat these severe and often chronic conditions. It is anticipated that acquiring and commercialising rare and orphan drugs could potentially lead to attractive revenue generation opportunities. Poolbeg will draw on the expertise of the wider team, including the individuals of the former Amryt team, who have a proven track record of successfully building and commercialising orphan drugs. Regulatory authorities offer incentives to companies developing orphan drugs, such as reduced filing fees, tax breaks and market exclusivity post approval and the Company Directors believe that Poolbeg is well positioned to benefit from these opportunities. The Company also announced further detail on the significant market opportunity for POLB 001 CRS induced by CAR-T and bispecific antibody treatments (BsAb), where CRS can affect the majority of patients and can lead to extended hospital stays, discontinuation of treatment and mortality risk. There are currently few approved therapies for the management of acute CRS and no preventative therapies indicated for CRS. The size and attractiveness of this market has encouraged the Company, as the field of cancer immunotherapies, including CAR-T and BsAb, is burgeoning and is expected to grow to USD 100 billion - USD 140 billion by 2030. CRS occurs in the majority of CAR-T and BsAb treatments frequently impacting >70% [iv] of patients and cannot be predicted. All grades of CRS can lead to extended hospital stays, causing an estimated USD 5.5 billion of hospitalisation costs to healthcare systems, and further indirect costs through patient treatment and follow up. An effective oral preventative therapy for cancer immunotherapy-induced CRS has the potential to significantly reduce direct costs in the healthcare system and improve patient access to these therapeutics, potentially including access to these therapies outside of specialist centres, while further augmenting wider market uptake. Poolbeg recently announced promising in vivo results for POLB 001 in addressing cancer immunotherapy-induced CRS, where CRS clinical symptoms were significantly improved by administration of POLB 001. Dose dependent reductions were seen in all serum proinflammatory cytokines measured.お知らせ • Jan 17Poolbeg Pharma plc Further Data Confirms Polb 001'S Potential in Cancer Immunotherapy-Induced Cytokine Release SyndromePoolbeg Pharma announced promising in vivo results for POLB 001 in addressing cancer immunotherapy-induced CRS. Positive study results POLB 001 demonstrated efficacy in reducing cancer immunotherapy-induced C RS in an in vivo animal model with CRS symptoms significantly improved following administration of POLB 001. Red reductions were seen in all serum proinflammatory cytokines tested. The results, together with the data from the recent LPS human challenge tria l, further support the Company's strategic expansion of the Phase II ready POLB 001 to treat and prevent cancer immunotherapy-induced CS. In the U.S., the American Cancer Society estimates that there will be 24.6 million cases of cancer by 2030. Cancer immunotherapies, such as bispecific antibodies and CAR T cell therapy, are rapidly moving into earlier lines of treatment in many tumour types, with these markets anticipated to grow to USD 100 billion+ (35% CAGR) by 2030.Board Change • Dec 31High number of new and inexperienced directorsThere are 7 new directors who have joined the board in the last 3 years. The company's board is composed of: 7 new directors. 1 experienced director. No highly experienced directors. Chairman of The Board Cathal Friel is the most experienced director on the board, commencing their role in 2021. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.お知らせ • Dec 20Poolbeg Pharma plc Announces Positive Outputs from Lab-Based Analysis of RSV Drug Candidates Identified Using AI RSV Drug Candidates with the High Probability of Successful Successful SuccessfullyPoolbeg Pharma announced the positive outputs from the lab-based analysis and successful prioritisation of the Respiratory Syncytial Virus ('RSV') drug targets and treatments identified as part of its artificial intelligence ('AI') led programme. Poolbeg's team of scientific experts have reviewed the comprehensive data package obtained from this lab-based analysis and has strategically prioritised a select number of the RSV drug candidates that were analysed. The Company is actively exploring the most effective way to progress the prioritised drug candidates in order to generate value. Poolbeg believes the data obtained reflects the high potential of this AI-led programme and supports its partnering efforts. The global interest in AI-led drug discovery continues to grow, with major pharmaceutical players making substantial investments in the field. Poolbeg's RSV AI programme identified these drug treatment candidates in just 10 months. AI-led drug discovery can accelerate the timeline achievable which reduces costs while also decreasing risks and providing a higher likelihood of success in bringing therapies to patients.お知らせ • Dec 11Poolbeg Pharma plc Announces Key Insights from Its Poster Presentation at ASH POLB 001Poolbeg Pharma announced key insights from its poster presentation at the 65th American Society of Hematology ('ASH') Annual Meeting and Exposition, San Diego. The poster, which details POLB 001 as a potential therapy for Cytokine Release Syndrome ('CRS') associated with cancer immunotherapies, was presented by Dr. Emma Searle from The Christie Hospital, Manchester, UK on Saturday 9 December. CRS is a well-recognised toxicity that occurs frequently following certain cancer treatments such as T-cell engaging antibodies and CAR T cell therapies. In addition to patient mortality and morbidity risk, the high frequency of CRS associated with these treatments represents a barrier to outpatient delivery. The need for in-patient management of CRS adds to the overall healthcare costs of delivering these treatments and contributes to restricting their availability. Meanwhile, the POLB 001 LPS human challenge trial conducted by Poolbeg demonstrated good safety and tolerability, a clear dose-response relationship, inhibition of p38 MAPK activation, and a reduction in all measured pro-inflammatory cytokines. The effects observed were a negation of immune over-reaction rather than an ablation of core immune function. Phase II trial enabling activities are underway with strong interest from potential pharma partners.お知らせ • Nov 30Poolbeg Pharma plc Announces Directorate ChangesPoolbeg Pharma PLC announces a change to its Board of Directors. Patrick Ashe, Independent Non-Executive Director, will step down from the Board at the end of November. Patrick played a significant role in guiding the Company through its initial phase of development. Eddie Gibson, Non-Executive Director will replace Patrick as Chair of the Audit & Risk Committee and Prof Brendan Buckley, Non-Executive Director will become Chair of the Remuneration Committee.お知らせ • Nov 09Poolbeg Pharma plc Announces Executive AppointmentsPoolbeg Pharma announced the appointment of key former executives of Amryt Pharma plc to its leadership team. David Allmond will join Poolbeg Pharma as Chief Business Officer from 1 December 2023. David was previously Chief Business Officer at Amryt and was instrumental in putting in place the global commercial infrastructure at Amryt which supported its revenue growth from c. USD 1.5 million when he joined in 2016, to approaching USD 250 million some six years later, when Amryt was sold to Chiesi Farmaceutici S.P.A. David played a pivotal role in Amryt, acquiring the Lojuxta distribution rights for Europe and the Middle East in 2016 and joined Amyrt thereafter. Lojuxta became Amryt's first approved, revenue generating product. David also played a very significant role in Amryt's acquisition of Aegerion in 2019 and Chiasma Pharmaceuticals in 2021. Previously, he played a key role leading the EMEA team at Aegerion Pharmaceuticals and was the Corporate Vice President of Global Marketing at Celgene during a period of very rapid growth for the company having previously established Celgene's UK operating company and led their marketing and market access team for EMEA. John McEvoy will become SVP, Chief Legal Officer, at Poolbeg from 1 January 2024. John was Global General Counsel at Amryt from 2017 and continued in his role at Amryt following its sale to Chiesi Farmaceutici S.P.A. earlier this year. John played an instrumental role in Amryt's rapid growth, leading the acquisition of Aegerion Pharmaceuticals in 2019 and Chiasma Pharmaceuticals in 2021. He also led the company's dual-listing on Nasdaq in 2020 and its subsequent sale to Chiesi. John is a qualified lawyer in the US (New York), England & Wales, and Ireland.お知らせ • Oct 27Poolbeg Pharma plc Announces Scientific Advisory Board Endorses Influenza Drug Targets Identified in Ai Drug Discovery ProgrammePoolbeg Pharma announced that its Scientific Advisory Board ('SAB') has endorsed the influenza drug targets identified in its AI-led drug discovery programme. The SAB was presented with comprehensive data and information regarding the large number of novel drug targets identified as part of the CytoReason collaboration in June 2023, along with a proposed list of prioritised candidates. Prioritisation was based on several key criteria and an evaluation by both Poolbeg and CytoReason's teams of expert biologists and data scientists to identify the top-ranking genes potentially suitable for the treatment of influenza. The members of the SAB considered the data and were impressed with the outputs of the programme, a consensus was reached on the prioritised list of novel drug targets to bring forward for lab-based validation, which is expected to complete in 2024. They also provided valuable insight into how to most effectively validate the targets in line with Poolbeg's model.分析記事 • Oct 05We're Hopeful That Poolbeg Pharma (LON:POLB) Will Use Its Cash WiselyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, biotech and mining...お知らせ • Sep 29Poolbeg Pharma PLC Announces Favourable Conclusion of Patent OppositionPoolbeg Pharma PLC announced that further to its announcement on 19 September 2023, the oral opposition hearing scheduled by the European Patent Office ('EPO') relating to the challenge to the Company's European patent (Immunomodulator I), has been cancelled. This favourably concludes this matter with the patent maintained as granted. The Immunomodulator I European patent was opposed by a third party in September 2021 and the opposition was subsequently withdrawn in September 2023. Following the opposition withdrawal, the EPO has now concluded that there is no need to proceed with the scheduled hearing, concluding this matter.お知らせ • Sep 21Poolbeg Pharma Receives Notice of Allowance from the Japanese Patent Office in Relation to its Immunomodulator I Patent ApplicationPoolbeg Pharma announced that it has received a notice of allowance from the Japanese Patent Office in relation to its Immunomodulator I patent application. The claims deemed allowable cover a p38 MAPK (mitogen-activated protein kinase) inhibitor for use in the treatment of severe influenza in human patients and strengthens the Company's robust intellectual property in the territory. Grant of the application as a patent is expected upon completion of formalities. Poolbeg has a worldwide licence for POLB 001 for all uses in humans and is developing a strong IP portfolio with patents in place, including Immunomodulator I and Immunomodulator II, covering the use of the class of p38 MAP kinase (mitogen-activated protein Kinase) inhibitors for the treatment of severe influenza and hypercytokinaemia. The Company has also filed patent applications to expand its IP around POLB 001 and the use of p38 MAP kinase inhibitors in new disease areas, such as oncology. This enhances the value and attractiveness of POLB 001 to potential pharma partners.お知らせ • Sep 19Poolbeg Pharma plc Announces Immunomodulator I Patent Opposition WithdrawalPoolbeg Pharma announced that the opposition to one of its European patents (Immunomodulator I) that was previously filed by a third party is to be withdrawn. In the pharmaceutical industry it is not unusual for patents to be challenged. The Immunomodulator I European patent was opposed by a third party in September 2021. Further to engaging with the opposing party, Poolbeg has reached an amicable conclusion in relation to the patent dispute without any financial compensation between the parties. The Company will be communicating with the European Patent Office ('EPO') regarding the necessity of continuing with the scheduled hearing in November. Based on specialist advice received, and the fact that the patent went through an extensive examination process prior to being granted by the EPO, Poolbeg continues to have full confidence in the validity and strength of the patent and will defend its intellectual property to the extent required. Poolbeg has a worldwide licence for POLB 001 for all uses in humans and is developing a strong IP portfolio with patents in place, including Immunomodulator I and Immunomodulator II, covering the use of the class of p38 MAP kinase (mitogen-activated protein kinase) inhibitors for the treatment of severe influenza and hypercytokinaemia. The Company has also filed patent applications to expand its IP around POLB 001 and the use of p38 MAP kinase inhibitors in new disease areas, such as oncology. This enhances the value and attractiveness of POLB 001 to potential pharma partners.New Risk • Aug 15New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of British stocks, typically moving 7.0% 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 Earnings are forecast to decline by an average of 14% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Less than 3 years of financial data is available. Currently unprofitable and not forecast to become profitable over next 2 years (UK£6.3m net loss in 2 years). Share price has been volatile over the past 3 months (7.0% average weekly change). Market cap is less than US$100m (UK£39.3m market cap, or US$50.0m).お知らせ • Jun 30Poolbeg Pharma plc Announces Significant Breakthrough in Its World First Influenza Artificial Intelligence Programme with CytoreasonPoolbeg Pharma announced a significant breakthrough in its world first influenza Artificial Intelligence ('AI') Programme with CytoReason. Poolbeg has been working with CytoReason since March 2022. Poolbeg's unique disease progression data from influenza human challenge trials combined with CytoReason's broad repositories of curated disease data were analysed using CytoReason's AI-led platform. The analysis has led to the discovery of multiple novel drug targets for the treatment of influenza. Identification of drug targets from this unique data-set has previously been successful as p38 MAP Kinase, inhibited by POLB 001, was identified as a driver of severe influenza but this required manual analysis that took several years. However, through the utilisation of CytoReason's cutting-edge AI technology, Poolbeg has now identified multiple novel drug targets in just 15 months. Moreover, CytoReason's analysis independently confirmed the significance of the p38 MAP kinase pathway in influenza, providing further validation for Poolbeg's POLB 001 programme. The Company is actively exploring the most effective way to further develop the novel drug targets in order to generate value and looks forward to updating shareholders about the progress of this programme in due course. Poolbeg Pharma has access to a unique repository of clinical samples and associated data from human challenge trials. Data from human challenge trials are unique in that they track a healthy subject through disease to recovery in carefully controlled and monitored isolation units, collecting samples throughout the course of disease, and vitally collecting matched baseline and follow-up samples before and after infection. This data is unique in the depth of longitudinal virology, health, biomarker and symptom data collected during the course of disease.Board Change • Jun 01Less than half of directors are independentFollowing the recent departure of a director, there are only 3 independent directors on the board. The company's board is composed of: 3 independent directors. 4 non-independent directors. Independent Non-Executive Director Patrick Ashe was the last independent director to join the board, commencing their role in 2021. The company's minority of independent directors is a risk according to the Simply Wall St Risk Model.分析記事 • Jun 01We're Hopeful That Poolbeg Pharma (LON:POLB) Will Use Its Cash WiselyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, although...お知らせ • May 24Poolbeg Pharma PLC Announces Board ChangesPoolbeg Pharma announced the appointment of Brendan Buckley as an Independent Non-Executive Director of the Company with immediate effect. Brendan will also replace Cathal Friel as a member of the Remuneration Committee. Professor Buckley is the former Chief Medical Officer of ICON plc, a medical graduate of University College Cork and a doctoral graduate in Biochemistry in the Faculty of Medicine at Oxford University. Prof Buckley has advised Poolbeg since inception and has deep experience in metabolic diseases including over 40 years' experience in clinical practice as a Consultant Physician in endocrinology, diabetes and in academic clinical pharmacology. Brendan was a member of the Board of Directors of the Irish Medicines Board (now the Health Products Regulatory Authority), chairing its statutory Advisory Committee for Human Medicines. He was also a member of the European Medicines Agency Committee for Orphan Medicinal Products (COMP) and of the European Medicines Agency Scientific Advisory Committee on diabetes and metabolism. Brendan has published over 150 scientific papers, mainly on metabolic disease, as well as the recent key opinion-leading book 'Re-Engineering Clinical Trials'. Mr. Brendan Mary Buckley, aged 73, has held the following directorships and/or partnerships in the past five years: Current directorships: hVIVO plc, FIGHTING BLINDNESS, DS BIOPHARMA LIMITED, Afimmune Limited, Open Orphan DAC, Imutex Ltd. Past directorships: BREAKTHROUGH CANCER RESEARCH and Alliance for Clinical Research Excellence and Safety Inc.お知らせ • Jan 16Poolbeg Pharma plc Announces Strategic Expansion of Polb 001 into OncologyPoolbeg Pharma announces the strategic expansion of POLB 001 into oncology. While investigating the role of cytokine release syndrome ("CRS") in severe influenza, Poolbeg discovered data specific to the overt immune response in CAR T cell patients that suggest POLB 001 as a potential treatment option for this severe complication. The Company has submitted a patent application for the use of POLB 001 in addressing the impact of CRS in CAR T cell patients.CAR T cell therapies are a form of immunotherapy for cancer that have produced remarkable results across a range of haematological malignancies, including cases of complete and durable responses in patients with advanced leukaemia and lymphoma who failed on previous therapies. A significant number of patients suffer treatment related side effects, including CRS which in severe form can be life threatening. Cell therapies may induce these effects in up to 95% of patients1. Poolbeg has identified POLB 001 as a potentially valuable companion therapy to be used in conjunction with existing CAR T cell therapies to address this significant unmet need. POLB 001's mode of action, reducing hyperinflammation which is associated with CRS, has the potential to significantly reduce the serious adverse effects experienced by many CAR T cell patients. The filed patent application is expected to provide class protection for use of p38 inhibitors in CAR T cell treatment and opens up a significant new market opportunity for POLB 001 in addition to severe influenza. A long-term strategic objective for Poolbeg has been and continues to be to evaluate POLB 001's potential in additional indications to fully unlock the potential value of the molecule and strengthen Poolbeg's position with a view to potential partnering and out-licensing. The Company is performing oncology clinical trial enabling activities to progress towards trial initiation in CAR T cell patients in 2024. Further oncology-related data, regulatory feedback and non-clinical development updates are expected in 2023.お知らせ • Jan 09Poolbeg Pharma PLC Announces Positive Initial Data Analysis in POLB 001 TrialPoolbeg Pharma PLC announced positive initial data analysis for POLB 001, a viral strain agnostic, small molecule immunomodulator being developed to address the significant unmet medical need for severe influenza. As announced in December, full data read-out is expected in Second Quarter 2023. However, upon initial review, the data indicates that administration of POLB 001 resulted in a marked reduction in both systemic and localised inflammatory response in subjects challenged with bacterial lipopolysaccharide ("LPS") compared to those who received placebo. A clear dose-response relationship was also apparent. This LPS challenge trial was designed to evaluate the effect of POLB 001 on inflammatory responses in 36 healthy volunteers between 18 and 55 years of age following both an intradermal and an intravenous LPS challenge. LPS acts as a surrogate for the hyperinflammatory response associated with severe influenza and other diseases. POLB 001 was well tolerated across all doses and no serious adverse events or volunteer withdrawals were reported.分析記事 • Jul 12Here's Why We're Not Too Worried About Poolbeg Pharma's (LON:POLB) Cash Burn SituationEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...Board Change • Apr 27No 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. Member of Scientific Advisory Board Daniel Hoft was the last director to join the board, commencing their role in 2021. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.お知らせ • Jul 20Poolbeg Pharma PLC has completed an IPO in the amount of £25 million.Poolbeg Pharma PLC has completed an IPO in the amount of £25 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 250,000,000 Price\Range: £0.1 Transaction Features: Regulation S株主還元POLBGB PharmaceuticalsGB 市場7D53.2%-5.5%-1.5%1Y161.5%16.2%17.2%株主還元を見る業界別リターン: POLB過去 1 年間で16.2 % の収益を上げたUK Pharmaceuticals業界を上回りました。リターン対市場: POLB過去 1 年間で17.2 % の収益を上げたUK市場を上回りました。価格変動Is POLB's price volatile compared to industry and market?POLB volatilityPOLB Average Weekly Movement8.7%Pharmaceuticals Industry Average Movement5.7%Market Average Movement5.6%10% most volatile stocks in GB Market11.7%10% least volatile stocks in GB Market3.1%安定した株価: POLBの株価は、 UK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: POLBの weekly volatility ( 9% ) は過去 1 年間安定していますが、依然としてUKの株式の 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202115Jeremy Skillingtonwww.poolbegpharma.comPoolbeg Pharma PLCはバイオ医薬品会社として、英国でアンメット・メディカル・ニーズに対する医薬品の開発・商業化に従事している。同社はPOLB 001を開発しており、がん免疫療法誘発性サイトカイン放出症候群と重症インフルエンザを対象に第1相臨床試験中である。また、肥満症および糖尿病治療のための経口カプセル化GLP-1Rアゴニスト、インフルエンザおよび呼吸器合胞体ウイルスのAIプログラム、呼吸器ウイルス感染症のためのファーストインクラスの広域スペクトラムRNAベース免疫療法であるPOLB 002、メリオイドーシスの予防のための筋肉内ワクチンであるPOLB 003を開発中である。さらに、免疫刺激抗原を腸の様々な部位に送達する経口ワクチン送達プラットフォームのカプセル化技術のライセンスも取得している。さらに同社は、重症化リスクを特定するためのバイオマーカープラットフォームや、新規ワクチン候補を特定するためのモデル由来の探索プラットフォームであるワクチン探索プラットフォームの開発にも携わっている。プールベッグ・ファーマは2021年に設立され、英国ロンドンに本社を置いている。もっと見るPoolbeg Pharma PLC 基礎のまとめPoolbeg Pharma の収益と売上を時価総額と比較するとどうか。POLB 基礎統計学時価総額UK£59.93m収益（TTM）-UK£5.69m売上高(TTM)n/a0.0xP/Sレシオ-10.5xPER（株価収益率POLB 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POLB 損益計算書（TTM）収益UK£0売上原価UK£0売上総利益UK£0その他の費用UK£5.70m収益-UK£5.69m直近の収益報告Dec 31, 2025次回決算日該当なし一株当たり利益（EPS）-0.0081グロス・マージン0.00%純利益率0.00%有利子負債／自己資本比率0%POLB 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2026/06/03 04:03終値2026/06/03 00:00収益2025/12/31年間収益2025/12/31データソース企業分析に使用したデータはS&P Global Market Intelligence LLC のものです。本レポートを作成するための分析モデルでは、以下のデータを使用しています。データは正規化されているため、ソースが利用可能になるまでに時間がかかる場合があります。パッケージデータタイムフレーム米国ソース例会社財務10年損益計算書キャッシュ・フロー計算書貸借対照表SECフォーム10-KSECフォーム10-Qアナリストのコンセンサス予想+プラス3年予想財務アナリストの目標株価アナリストリサーチレポートBlue Matrix市場価格30年株価配当、分割、措置ICEマーケットデータSECフォームS-1所有権10年トップ株主インサイダー取引SECフォーム4SECフォーム13Dマネジメント10年リーダーシップ・チーム取締役会SECフォーム10-KSECフォームDEF 14A主な進展10年会社からのお知らせSECフォーム8-K* 米国証券を対象とした例であり、非米国証券については、同等の規制書式および情報源を使用。特に断りのない限り、すべての財務データは1年ごとの期間に基づいていますが、四半期ごとに更新されます。これは、TTM（Trailing Twelve Month）またはLTM（Last Twelve Month）データとして知られています。詳細はこちら。分析モデルとスノーフレーク本レポートを生成するために使用した分析モデルの詳細は当社のGithubページでご覧いただけます。また、レポートの使用方法に関するガイドやYoutubeのチュートリアルも掲載しています。シンプリー・ウォールストリート分析モデルを設計・構築した世界トップクラスのチームについてご紹介します。業界およびセクターの指標私たちの業界とセクションの指標は、Simply Wall Stによって6時間ごとに計算されます。アナリスト筋Poolbeg Pharma PLC 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Adam McCarterCavendishBrian WhiteShore Capital Group Ltd
お知らせ • May 11Poolbeg Pharma Receives Patent Grant For POLB 001 Cancer Immunotherapy-Induced CRS In CanadaPoolbeg Pharma had received formal notification of the grant for its POLB 001 cancer immunotherapy-induced Cytokine Release Syndrome patent application from the Canadian patent office. This represents the second national grant within Poolbeg's cancer immunotherapy-induced CRS patent family, following the grant by IP Australia announced in March 2026, and marks a further important milestone for the Company. This patent covers the use of any p38 MAPK inhibitor, including POLB 001, for the prevention of cancer immunotherapy-induced CRS, and is underpinned by proprietary data generated by Poolbeg. Poolbeg filed its initial oncology patent applications in the UK in January 2023 before entering the international Patent Cooperation Treaty system in January 2024. This new patent grant was accelerated through the Patent Prosecution Highway, which enables expedited examination in participating countries where a favourable ruling has already been secured in another participating jurisdiction. The Company's IP portfolio now spans both cancer immunotherapy-induced CRS and severe influenza across multiple jurisdictions, and Poolbeg continues to pursue protection in further territories. This grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's future value and appeal to potential partners.
お知らせ • May 07Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026. Location: the offices of gravita at aldgate tower, 2 leman street, e1 8fa, london United Kingdom
お知らせ • Apr 17Poolbeg Pharma plc Receives Clinical Trial Authorisation for Polb 001 Topical TrialPoolbeg Pharma announced that the UK Medicines and Healthcare products Regulatory Agency ("MHRA") has granted Clinical Trial Authorisation ("CTA") for the POLB 001 TOPICAL trial. With all required regulatory clearances now in place and site initiation visits scheduled, the trial remains on track to deliver interim data this summer. The Company also announces positive findings from new independent US focused payer research conducted by Acumetis Global indicates multi-billion-dollar peak sales potential in the United States. POLB 001 is being developed as a potential first approved preventative therapy for cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"). The TOPICAL trial will investigate POLB 001 in approximately 30 relapsed/refractory multiple myeloma patients receiving the approved bispecific antibody teclistamab, which has been supplied by Johnson & Johnson at no cost to Poolbeg. The study now spans six sites across the UK, with NHS Lothian in Edinburgh and the Royal Stoke University Hospital joining existing sites at the NHS Trusts at The Christie, The Royal Marsden, University College London Hospitals, and University Hospitals Birmingham. Site initiation visits are scheduled with patient screening set to commence shortly. Unlike many oncology studies, given that CRS is an acute condition which occurs within days or weeks of initiation of a bispecific antibody, the design of the TOPICAL trial will allow rapid read out. The research, which engaged current payers covering approximately 75 million lives across a mix of commercial insurance providers, Medicare and Medicaid, confirms the strong, clearly defined value proposition for POLB 001. In particular, findings underscore POLB 001's potential to play an important role in the management of CRS by reducing the significant hospital costs associated with the condition and enabling a meaningful shift in care away from specialist centres of excellence toward outpatient and community settings. The report also noted that CRS occurs in the majority of CAR T and bispecific antibody treatments, with no established diagnostic method currently available to predict either the likelihood or severity of CRS in individual patients. Dosing of bispecific antibodies must be withheld until CRS resolves, often delaying patients from achieving therapeutically effective dosing levels and prolonging hospitalisation, while those who experience high-grade CRS must permanently discontinue treatment, meaning that these patients can no longer receive the potentially life-saving treatment. The research reconfirmed the significant cost burden associated with managing CRS and that an effective preventative treatment would represent a compelling value proposition for healthcare systems. The findings highlight pricing levels that demonstrate POLB 001's multi-billion-dollar peak sales potential, providing increased confidence in the Company's anticipated market opportunity and further supports POLB 001's future value and appeal to potential partners.
お知らせ • Nov 22Poolbeg Pharma plc Receives European Immunomodulator II Patent Application Covering POLB 001 for the Treatment of Severe InfluenzaPoolbeg Pharma announced that the European Patent Office has granted Poolbeg's European Immunomodulator II patent application covering POLB 001 for the treatment of severe influenza. POLB 001 is a potent and selective p38 MAP kinase inhibitor with strong potential across multiple disease areas, including the prevention and treatment of cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"), a potential market opportunity of over USD 10 billion, and the treatment of severe influenza. POLB 001 holds the potential to address significant unmet needs affecting patients and healthcare systems globally. Poolbeg is actively building a comprehensive, worldwide IP portfolio, with patents covering use of p38 MAPK inhibitors in patients with severe influenza and for the prevention and treatment of cancer Immunotherapy-induced CRS. This patent grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's value and appeal to potential partners.
お知らせ • May 27Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025. Location: the offices of dac beachcroft llp, 25 walbrook, ec4n 8af, london United Kingdom
お知らせ • May 23Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million.Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 6,000,000 Price\Range: £0.025
お知らせ • May 11Poolbeg Pharma Receives Patent Grant For POLB 001 Cancer Immunotherapy-Induced CRS In CanadaPoolbeg Pharma had received formal notification of the grant for its POLB 001 cancer immunotherapy-induced Cytokine Release Syndrome patent application from the Canadian patent office. This represents the second national grant within Poolbeg's cancer immunotherapy-induced CRS patent family, following the grant by IP Australia announced in March 2026, and marks a further important milestone for the Company. This patent covers the use of any p38 MAPK inhibitor, including POLB 001, for the prevention of cancer immunotherapy-induced CRS, and is underpinned by proprietary data generated by Poolbeg. Poolbeg filed its initial oncology patent applications in the UK in January 2023 before entering the international Patent Cooperation Treaty system in January 2024. This new patent grant was accelerated through the Patent Prosecution Highway, which enables expedited examination in participating countries where a favourable ruling has already been secured in another participating jurisdiction. The Company's IP portfolio now spans both cancer immunotherapy-induced CRS and severe influenza across multiple jurisdictions, and Poolbeg continues to pursue protection in further territories. This grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's future value and appeal to potential partners.
お知らせ • May 07Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026Poolbeg Pharma PLC, Annual General Meeting, Jun 09, 2026. Location: the offices of gravita at aldgate tower, 2 leman street, e1 8fa, london United Kingdom
お知らせ • Apr 17Poolbeg Pharma plc Receives Clinical Trial Authorisation for Polb 001 Topical TrialPoolbeg Pharma announced that the UK Medicines and Healthcare products Regulatory Agency ("MHRA") has granted Clinical Trial Authorisation ("CTA") for the POLB 001 TOPICAL trial. With all required regulatory clearances now in place and site initiation visits scheduled, the trial remains on track to deliver interim data this summer. The Company also announces positive findings from new independent US focused payer research conducted by Acumetis Global indicates multi-billion-dollar peak sales potential in the United States. POLB 001 is being developed as a potential first approved preventative therapy for cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"). The TOPICAL trial will investigate POLB 001 in approximately 30 relapsed/refractory multiple myeloma patients receiving the approved bispecific antibody teclistamab, which has been supplied by Johnson & Johnson at no cost to Poolbeg. The study now spans six sites across the UK, with NHS Lothian in Edinburgh and the Royal Stoke University Hospital joining existing sites at the NHS Trusts at The Christie, The Royal Marsden, University College London Hospitals, and University Hospitals Birmingham. Site initiation visits are scheduled with patient screening set to commence shortly. Unlike many oncology studies, given that CRS is an acute condition which occurs within days or weeks of initiation of a bispecific antibody, the design of the TOPICAL trial will allow rapid read out. The research, which engaged current payers covering approximately 75 million lives across a mix of commercial insurance providers, Medicare and Medicaid, confirms the strong, clearly defined value proposition for POLB 001. In particular, findings underscore POLB 001's potential to play an important role in the management of CRS by reducing the significant hospital costs associated with the condition and enabling a meaningful shift in care away from specialist centres of excellence toward outpatient and community settings. The report also noted that CRS occurs in the majority of CAR T and bispecific antibody treatments, with no established diagnostic method currently available to predict either the likelihood or severity of CRS in individual patients. Dosing of bispecific antibodies must be withheld until CRS resolves, often delaying patients from achieving therapeutically effective dosing levels and prolonging hospitalisation, while those who experience high-grade CRS must permanently discontinue treatment, meaning that these patients can no longer receive the potentially life-saving treatment. The research reconfirmed the significant cost burden associated with managing CRS and that an effective preventative treatment would represent a compelling value proposition for healthcare systems. The findings highlight pricing levels that demonstrate POLB 001's multi-billion-dollar peak sales potential, providing increased confidence in the Company's anticipated market opportunity and further supports POLB 001's future value and appeal to potential partners.
お知らせ • Nov 22Poolbeg Pharma plc Receives European Immunomodulator II Patent Application Covering POLB 001 for the Treatment of Severe InfluenzaPoolbeg Pharma announced that the European Patent Office has granted Poolbeg's European Immunomodulator II patent application covering POLB 001 for the treatment of severe influenza. POLB 001 is a potent and selective p38 MAP kinase inhibitor with strong potential across multiple disease areas, including the prevention and treatment of cancer immunotherapy-induced Cytokine Release Syndrome ("CRS"), a potential market opportunity of over USD 10 billion, and the treatment of severe influenza. POLB 001 holds the potential to address significant unmet needs affecting patients and healthcare systems globally. Poolbeg is actively building a comprehensive, worldwide IP portfolio, with patents covering use of p38 MAPK inhibitors in patients with severe influenza and for the prevention and treatment of cancer Immunotherapy-induced CRS. This patent grant further strengthens the Company's robust intellectual property portfolio, enhancing POLB 001's value and appeal to potential partners.
お知らせ • May 27Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025Poolbeg Pharma PLC, Annual General Meeting, Jun 23, 2025. Location: the offices of dac beachcroft llp, 25 walbrook, ec4n 8af, london United Kingdom
お知らせ • May 23Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million.Poolbeg Pharma PLC has completed a Follow-on Equity Offering in the amount of £0.15 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 6,000,000 Price\Range: £0.025
お知らせ • May 20+ 1 more updatePoolbeg Pharma PLC has filed a Follow-on Equity Offering in the amount of £0.1 million.Poolbeg Pharma PLC has filed a Follow-on Equity Offering in the amount of £0.1 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 4,000,000 Price\Range: £0.025
お知らせ • Mar 20Poolbeg Pharma plc Receives Korean Intellectual Property Office Grant in KoreaPoolbeg Pharma announced that the Korean Intellectual Property Office has notified the Company of its official decision to grant Poolbeg's Republic of Korea Immunomodulator II patent application providing protection to POLB 001 for the treatment of severe influenza to December 2038. POLB 001 is a potent and selective p38 MAP kinase inhibitor with strong potential across multiple disease areas, including the prevention and treatment of cancer immunotherapy-induced Cytokine Release Syndrome and severe influenza. POLB 001 holds the potential to address significant unmet needs affecting patients and healthcare systems globally. This patent grant further strengthens Poolbeg's IP portfolio. Poolbeg has a robust portfolio of patents in place covering p38 MAP kinase inhibitors for the treatment of severe influenza; and for POLB 001 for the prevention or treatment of hypercytokinemia. Additional patent applications have been filed to strengthen and complement Poolbeg's POLB 001 patent portfolio, particularly for cytokine release syndrome caused by cancer immunotherapies. Developing a strong intellectual property portfolio remains a key priority for Poolbeg, enhancing POLB 001's value and appeal to potential partners.
お知らせ • Jan 03Poolbeg Expects to Become A Private Subsidiary of HOOKIPA and Apply for Cancellation of the Admission of Its Shares to Trading on AIMThe boards of directors (each a “Board”) of HOOKIPA Pharma Inc. (“HOOKIPA”) and Poolbeg Pharma plc (“Poolbeg”) are pleased to announce that they have entered into non-binding discussions for an all-share acquisition by HOOKIPA of Poolbeg (the “Potential Combination”) to create a strong clinical-stage biopharmaceutical company focused on developing and commercialising innovative medicines for critical unmet medical needs, with a special focus on next-generation immunotherapies for the treatment of cancer and other serious diseases (the “Combined Group”). HOOKIPA intends to remain as the listed entity for the Combined Group on the Nasdaq Capital Market and Poolbeg is expected to become a private subsidiary of HOOKIPA and apply for cancellation of the admission of its shares to trading on AIM.
New Risk • Jan 02New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of British stocks, typically moving 13% a week. This is considered a major risk. Share price volatility 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. It may also indicate 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. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (13% average weekly change). Earnings are forecast to decline by an average of 13% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable next year (UK£6.0m net loss next year). Market cap is less than US$100m (UK£21.4m market cap, or US$26.4m).
お知らせ • Jan 02Poolbeg Pharma PLC (AIM:POLB) entered into non-binding discussions to acquire HOOKIPA Pharma Inc. (NasdaqCM:HOOK) for $1.3 million in a reverse merger transaction.Poolbeg Pharma PLC (AIM:POLB) entered into non-binding discussions to acquire HOOKIPA Pharma Inc. (NasdaqCM:HOOK) for $1.3 million in a reverse merger transaction on January 2, 2025. The Boards believe that the Potential Combination would create a Nasdaq-listed Combined Group operated by a combined management team. Poolbeg shareholders will receive 0.03 HOOKIPA shares for each Poolbeg share held (the “ Exchange Ratio ”); based on the Exchange Ratio, the Potential Combination would have the effect (on the basis of the assumptions set out below and prior to the dilution resulting from the Fundraise (as defined below)) that Poolbeg shareholders prior to the completion of the Potential Combination are expected to receive, on a fully diluted basis, approximately 55% of the equity in the Combined Group (the “ Poolbeg Ownership Percentage ”) and HOOKIPA shareholders are expected to hold approximately 45% of the equity in the Combined Group (the “ HOOKIPA Ownership Percentage ”); HOOKIPA is expected to undertake a 100% primary private placement fundraise of up to approximately $30 million (the “ Fundraise ”) which will be funded into HOOKIPA immediately following the completion of the Potential Combination; a percentage of the potential value from certain of HOOKIPA’s programmes will be retained by holders of HOOKIPA shares as at a date to be determined ahead of completion of the Potential Combination (“ HOOKIPA Shareholders ”) via a contingent value right instrument (“ CVR ”); HOOKIPA intends to remain as the listed entity for the Combined Group on the Nasdaq Capital Market and Poolbeg is expected to become a private subsidiary of HOOKIPA and apply for cancellation of the admission of its shares to trading on AIM; and The Combined Group is expected to have operations in the European Union, the United Kingdom and the United States of America, and anticipates benefiting from a strong international leadership team comprised of the following individuals: Malte Peters: Chief Executive Officer, Cathal Friel: Poolbeg Co-Founder, Ian O’Connell: Chief Financial Officer, Poolbeg Co-Founder, Mark Winderlich: Chief Development Officer, David Allmond: Chief Business Officer and John McEvoy: Chief Legal Officer. Combination is subject to the satisfaction or waiver of a number of customary pre-conditions, including, amongst other things, the satisfactory completion of customary due diligence, finalisation of the terms of the transaction, Board approvals of binding terms and sufficient prior expressions of interest from participants in respect to the Fundraise. The Potential Combination would be subject to the approval of both HOOKIPA and Poolbeg shareholders and other conditions. Geoff Nash, Henrik Persson, Hamish Waller and Trisyia Jamaludin of Cavendish Capital Markets Ltd?acted as financial advisors to Poolbeg Pharma. Eugene Rozelman, David Coatenand and Harry Davies-Ball of Canaccord Genuity acted as financial advisors to Poolbeg Pharma. Chris Raff and Simon Chaudhuri from London office and Ashish Contractor from New York office of Moelis & Company acted as financial advisors to HOOKIPA.
お知らせ • Nov 20Poolbeg Pharma plc Announces U.S. Patent Office Grants U.S. Immunomodulator I PatentPoolbeg Pharma announced that the U.S. Patent Office has notified the Company of its official decision to grant Poolbeg's US Immunomodulator I patent application. The claims cover POLB 001, and other p38 MAP kinase inhibitors, for the treatment of patients at risk of severe influenza after an immune response has been triggered, and for the treatment of hypercytokinemia (cytokine storm) characteristic of severe influenza. POLB 001 is a potent and selective Phase II-ready p38 MAP kinase inhibitor with strong potential across multiple disease areas. This patent grant further strengthens Poolbeg's robust Intellectual Property (IP) portfolio. The Company has patents in place covering p38 MAP kinase inhibitors for the treatment of severe influenza; and covering POLB 001 for the treatment of hypercyTokinemia. Further patent applications have been filed and have complementary coverage as the Company continues to expand its patent portfolio covering POLB 001 and the wider class of p38 MAP kinase inhibitors., particularly in respect of cytokine release syndrome induced by cancer immunotherapies. Building a robust IP portfolio is a key focus for Poolbeg to further enhance POLB 001's value and attractiveness to potential partners.
分析記事 • Aug 20Companies Like Poolbeg Pharma (LON:POLB) Are In A Position To Invest In GrowthJust because a business does not make any money, does not mean that the stock will go down. For example, although...
お知らせ • Jul 26Poolbeg Pharma Announces Voluntary Delist from OTCQB MarketPoolbeg Pharma PLC announced that it is voluntarily delisting its ordinary shares (‘Ordinary Shares’) from trading on the OTCQB Market due to low trading volume and the associated administrative requirements. The company's last day of trading on the OTCQB Market will be 29 July 2024. Poolbeg will retain its listing on the London Stock Exchange's AIM Market under its existing ticker ‘POLB’. The delisting from the OTCQB market will have no impact on Poolbeg's Ordinary Shares, which will continue to trade on the AIM Market. Poolbeg reaffirms its ambitions to be dual listed on a national securities exchange in the US, such as Nasdaq, subject to meeting their listing requirements at the appropriate time.
お知らせ • May 11Poolbeg Pharma PLC, Annual General Meeting, Jun 13, 2024Poolbeg Pharma PLC, Annual General Meeting, Jun 13, 2024. Location: the offices of dac beachcroft llp, 25 walbrook, ec4n 8af, london United Kingdom
お知らせ • May 03Poolbeg Pharma PLC Receives the Fully Granted Patent from the U.S. Patent Office for Its Immunomodulator II Patent ApplicationPoolbeg Pharma PLC announced that further to its announcement on 20 March 2024, the Company has received the fully granted patent from the U.S Patent Office for its Immunomodulator II patent application. The claims cover a class of drugs (including POLB 001) for treating hypercytokinaemia (cytokine storm) and for preventing hypercytokinaemia in a patient after an immune response has been triggered. This encompasses cytokine storm that is induced in any disease indication. This further strengthens the Company's robust intellectual property portfolio for POLB 001, thereby enhancing the value and attractiveness of POLB 001 to potential Pharma partners. Poolbeg is actively building a comprehensive and worldwide IP portfolio, with patents in place covering p38 MAP kinase inhibitors for the treatment of severe influenza; and covering POLB 001 for the treatment of hypercytokinaemia. Further patent applications have been filed and have complementary coverage as the Company continues to expand its patent portfolio covering POLB 001 and the wider class of p38 MAP kinase inhibitors, particularly in respect of the treatment of cytokine release syndrome following cancer immunotherapy.
New Risk • Mar 31New minor risk - Financial data availabilityThe company's latest financial reports are more than 6 months old. Last reported fiscal period ended June 2023. This is considered a minor risk. If the company has not reported its earnings on time, it may have been delayed due to audit problems or it may be finding it difficult to reconcile its accounts. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 14% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Latest financial reports are more than 6 months old (reported June 2023 fiscal period end). Currently unprofitable and not forecast to become profitable next year (UK£5.8m net loss next year). Market cap is less than US$100m (UK£49.3m market cap, or US$62.1m).
Recent Insider Transactions • Feb 22Executive Chairman of The Board recently bought UK£97k worth of stockOn the 19th of February, Cathal Friel bought around 830k shares on-market at roughly UK£0.12 per share. This transaction amounted to 2.3% of their direct individual holding at the time of the trade. This was the largest purchase by an insider in the last 3 months. This was Cathal's only on-market trade for the last 12 months.
分析記事 • Feb 16We're Hopeful That Poolbeg Pharma (LON:POLB) Will Use Its Cash WiselyEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
お知らせ • Feb 15Poolbeg Pharma plc Appoints Cathal Friel as Executive ChairmanPoolbeg Pharma plc announced a change of Board role. Cathal Friel, Co-Founder, substantial shareholder, and currently Non-Executive Chairman of the company is assuming the role of Executive Chairman at the company effective immediately. Cathal brings valuable experience from his longstanding track record of value creation in a number of public companies, including as Co-Founder of Amryt Pharma plc. He was also the Executive Chairman and Co-Founder of hVIVO plc. Since then, Cathal and his team have transformed hVIVO into a fast growing, profitable company with revenues of over £56 million, a share price of c. 28 pence and a market capitalisation of c. £200 million. Cathal will continue to work closely with the Company's Chief Executive Officer, Jeremy Skillington and the now expanded leadership team, several of whom have recently joined from Amryt Pharma. Cathal will focus on it's strategic initiatives, leveraging his strong track record of value creation, including the company's growing focus upon rare and orphan diseases, whilst Jeremy will continue his successful leadership of the company's clinical programmes and business development efforts alongside David Allmond.
お知らせ • Feb 12Independent Research Confirms >$10 Billion Market Opportunity for POLB 001 as A Preventative Therapy for Cancer Immunotherapy-Induced Cytokine Release Syndrome (CRS)Poolbeg Pharma PLC announced that independent research conducted on behalf of Poolbeg confirms a >$10 billion market opportunity for POLB 001 in Cancer Immunotherapy-Induced CRS as an orally delivered preventative therapy. Cancer immunotherapies have been approved in rare and orphan blood cancers and so the Company can see potential for POLB 001 in one or more of these cancer types. POLB 001 in cancer immunotherapy-induced CRS will be developed alongside Poolbeg's existing portfolio of assets including its influenza programme; its AI drug discovery programmes; and oral delivery of GLP-1 for obesity and other metabolic diseases. Rare and orphan diseases represent a significant value creation opportunity for the Company and its shareholders as they are underserved and there remains a substantial opportunity for innovative medicines to treat these severe and often chronic conditions. It is anticipated that acquiring and commercialising rare and orphan drugs could potentially lead to attractive revenue generation opportunities. Poolbeg will draw on the expertise of the wider team, including the individuals of the former Amryt team, who have a proven track record of successfully building and commercialising orphan drugs. Regulatory authorities offer incentives to companies developing orphan drugs, such as reduced filing fees, tax breaks and market exclusivity post approval and the Company Directors believe that Poolbeg is well positioned to benefit from these opportunities. The Company also announced further detail on the significant market opportunity for POLB 001 CRS induced by CAR-T and bispecific antibody treatments (BsAb), where CRS can affect the majority of patients and can lead to extended hospital stays, discontinuation of treatment and mortality risk. There are currently few approved therapies for the management of acute CRS and no preventative therapies indicated for CRS. The size and attractiveness of this market has encouraged the Company, as the field of cancer immunotherapies, including CAR-T and BsAb, is burgeoning and is expected to grow to USD 100 billion - USD 140 billion by 2030. CRS occurs in the majority of CAR-T and BsAb treatments frequently impacting >70% [iv] of patients and cannot be predicted. All grades of CRS can lead to extended hospital stays, causing an estimated USD 5.5 billion of hospitalisation costs to healthcare systems, and further indirect costs through patient treatment and follow up. An effective oral preventative therapy for cancer immunotherapy-induced CRS has the potential to significantly reduce direct costs in the healthcare system and improve patient access to these therapeutics, potentially including access to these therapies outside of specialist centres, while further augmenting wider market uptake. Poolbeg recently announced promising in vivo results for POLB 001 in addressing cancer immunotherapy-induced CRS, where CRS clinical symptoms were significantly improved by administration of POLB 001. Dose dependent reductions were seen in all serum proinflammatory cytokines measured.
お知らせ • Jan 17Poolbeg Pharma plc Further Data Confirms Polb 001'S Potential in Cancer Immunotherapy-Induced Cytokine Release SyndromePoolbeg Pharma announced promising in vivo results for POLB 001 in addressing cancer immunotherapy-induced CRS. Positive study results POLB 001 demonstrated efficacy in reducing cancer immunotherapy-induced C RS in an in vivo animal model with CRS symptoms significantly improved following administration of POLB 001. Red reductions were seen in all serum proinflammatory cytokines tested. The results, together with the data from the recent LPS human challenge tria l, further support the Company's strategic expansion of the Phase II ready POLB 001 to treat and prevent cancer immunotherapy-induced CS. In the U.S., the American Cancer Society estimates that there will be 24.6 million cases of cancer by 2030. Cancer immunotherapies, such as bispecific antibodies and CAR T cell therapy, are rapidly moving into earlier lines of treatment in many tumour types, with these markets anticipated to grow to USD 100 billion+ (35% CAGR) by 2030.
Board Change • Dec 31High number of new and inexperienced directorsThere are 7 new directors who have joined the board in the last 3 years. The company's board is composed of: 7 new directors. 1 experienced director. No highly experienced directors. Chairman of The Board Cathal Friel is the most experienced director on the board, commencing their role in 2021. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors.
お知らせ • Dec 20Poolbeg Pharma plc Announces Positive Outputs from Lab-Based Analysis of RSV Drug Candidates Identified Using AI RSV Drug Candidates with the High Probability of Successful Successful SuccessfullyPoolbeg Pharma announced the positive outputs from the lab-based analysis and successful prioritisation of the Respiratory Syncytial Virus ('RSV') drug targets and treatments identified as part of its artificial intelligence ('AI') led programme. Poolbeg's team of scientific experts have reviewed the comprehensive data package obtained from this lab-based analysis and has strategically prioritised a select number of the RSV drug candidates that were analysed. The Company is actively exploring the most effective way to progress the prioritised drug candidates in order to generate value. Poolbeg believes the data obtained reflects the high potential of this AI-led programme and supports its partnering efforts. The global interest in AI-led drug discovery continues to grow, with major pharmaceutical players making substantial investments in the field. Poolbeg's RSV AI programme identified these drug treatment candidates in just 10 months. AI-led drug discovery can accelerate the timeline achievable which reduces costs while also decreasing risks and providing a higher likelihood of success in bringing therapies to patients.
お知らせ • Dec 11Poolbeg Pharma plc Announces Key Insights from Its Poster Presentation at ASH POLB 001Poolbeg Pharma announced key insights from its poster presentation at the 65th American Society of Hematology ('ASH') Annual Meeting and Exposition, San Diego. The poster, which details POLB 001 as a potential therapy for Cytokine Release Syndrome ('CRS') associated with cancer immunotherapies, was presented by Dr. Emma Searle from The Christie Hospital, Manchester, UK on Saturday 9 December. CRS is a well-recognised toxicity that occurs frequently following certain cancer treatments such as T-cell engaging antibodies and CAR T cell therapies. In addition to patient mortality and morbidity risk, the high frequency of CRS associated with these treatments represents a barrier to outpatient delivery. The need for in-patient management of CRS adds to the overall healthcare costs of delivering these treatments and contributes to restricting their availability. Meanwhile, the POLB 001 LPS human challenge trial conducted by Poolbeg demonstrated good safety and tolerability, a clear dose-response relationship, inhibition of p38 MAPK activation, and a reduction in all measured pro-inflammatory cytokines. The effects observed were a negation of immune over-reaction rather than an ablation of core immune function. Phase II trial enabling activities are underway with strong interest from potential pharma partners.
お知らせ • Nov 30Poolbeg Pharma plc Announces Directorate ChangesPoolbeg Pharma PLC announces a change to its Board of Directors. Patrick Ashe, Independent Non-Executive Director, will step down from the Board at the end of November. Patrick played a significant role in guiding the Company through its initial phase of development. Eddie Gibson, Non-Executive Director will replace Patrick as Chair of the Audit & Risk Committee and Prof Brendan Buckley, Non-Executive Director will become Chair of the Remuneration Committee.
お知らせ • Nov 09Poolbeg Pharma plc Announces Executive AppointmentsPoolbeg Pharma announced the appointment of key former executives of Amryt Pharma plc to its leadership team. David Allmond will join Poolbeg Pharma as Chief Business Officer from 1 December 2023. David was previously Chief Business Officer at Amryt and was instrumental in putting in place the global commercial infrastructure at Amryt which supported its revenue growth from c. USD 1.5 million when he joined in 2016, to approaching USD 250 million some six years later, when Amryt was sold to Chiesi Farmaceutici S.P.A. David played a pivotal role in Amryt, acquiring the Lojuxta distribution rights for Europe and the Middle East in 2016 and joined Amyrt thereafter. Lojuxta became Amryt's first approved, revenue generating product. David also played a very significant role in Amryt's acquisition of Aegerion in 2019 and Chiasma Pharmaceuticals in 2021. Previously, he played a key role leading the EMEA team at Aegerion Pharmaceuticals and was the Corporate Vice President of Global Marketing at Celgene during a period of very rapid growth for the company having previously established Celgene's UK operating company and led their marketing and market access team for EMEA. John McEvoy will become SVP, Chief Legal Officer, at Poolbeg from 1 January 2024. John was Global General Counsel at Amryt from 2017 and continued in his role at Amryt following its sale to Chiesi Farmaceutici S.P.A. earlier this year. John played an instrumental role in Amryt's rapid growth, leading the acquisition of Aegerion Pharmaceuticals in 2019 and Chiasma Pharmaceuticals in 2021. He also led the company's dual-listing on Nasdaq in 2020 and its subsequent sale to Chiesi. John is a qualified lawyer in the US (New York), England & Wales, and Ireland.
お知らせ • Oct 27Poolbeg Pharma plc Announces Scientific Advisory Board Endorses Influenza Drug Targets Identified in Ai Drug Discovery ProgrammePoolbeg Pharma announced that its Scientific Advisory Board ('SAB') has endorsed the influenza drug targets identified in its AI-led drug discovery programme. The SAB was presented with comprehensive data and information regarding the large number of novel drug targets identified as part of the CytoReason collaboration in June 2023, along with a proposed list of prioritised candidates. Prioritisation was based on several key criteria and an evaluation by both Poolbeg and CytoReason's teams of expert biologists and data scientists to identify the top-ranking genes potentially suitable for the treatment of influenza. The members of the SAB considered the data and were impressed with the outputs of the programme, a consensus was reached on the prioritised list of novel drug targets to bring forward for lab-based validation, which is expected to complete in 2024. They also provided valuable insight into how to most effectively validate the targets in line with Poolbeg's model.
分析記事 • Oct 05We're Hopeful That Poolbeg Pharma (LON:POLB) Will Use Its Cash WiselyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, biotech and mining...
お知らせ • Sep 29Poolbeg Pharma PLC Announces Favourable Conclusion of Patent OppositionPoolbeg Pharma PLC announced that further to its announcement on 19 September 2023, the oral opposition hearing scheduled by the European Patent Office ('EPO') relating to the challenge to the Company's European patent (Immunomodulator I), has been cancelled. This favourably concludes this matter with the patent maintained as granted. The Immunomodulator I European patent was opposed by a third party in September 2021 and the opposition was subsequently withdrawn in September 2023. Following the opposition withdrawal, the EPO has now concluded that there is no need to proceed with the scheduled hearing, concluding this matter.
お知らせ • Sep 21Poolbeg Pharma Receives Notice of Allowance from the Japanese Patent Office in Relation to its Immunomodulator I Patent ApplicationPoolbeg Pharma announced that it has received a notice of allowance from the Japanese Patent Office in relation to its Immunomodulator I patent application. The claims deemed allowable cover a p38 MAPK (mitogen-activated protein kinase) inhibitor for use in the treatment of severe influenza in human patients and strengthens the Company's robust intellectual property in the territory. Grant of the application as a patent is expected upon completion of formalities. Poolbeg has a worldwide licence for POLB 001 for all uses in humans and is developing a strong IP portfolio with patents in place, including Immunomodulator I and Immunomodulator II, covering the use of the class of p38 MAP kinase (mitogen-activated protein Kinase) inhibitors for the treatment of severe influenza and hypercytokinaemia. The Company has also filed patent applications to expand its IP around POLB 001 and the use of p38 MAP kinase inhibitors in new disease areas, such as oncology. This enhances the value and attractiveness of POLB 001 to potential pharma partners.
お知らせ • Sep 19Poolbeg Pharma plc Announces Immunomodulator I Patent Opposition WithdrawalPoolbeg Pharma announced that the opposition to one of its European patents (Immunomodulator I) that was previously filed by a third party is to be withdrawn. In the pharmaceutical industry it is not unusual for patents to be challenged. The Immunomodulator I European patent was opposed by a third party in September 2021. Further to engaging with the opposing party, Poolbeg has reached an amicable conclusion in relation to the patent dispute without any financial compensation between the parties. The Company will be communicating with the European Patent Office ('EPO') regarding the necessity of continuing with the scheduled hearing in November. Based on specialist advice received, and the fact that the patent went through an extensive examination process prior to being granted by the EPO, Poolbeg continues to have full confidence in the validity and strength of the patent and will defend its intellectual property to the extent required. Poolbeg has a worldwide licence for POLB 001 for all uses in humans and is developing a strong IP portfolio with patents in place, including Immunomodulator I and Immunomodulator II, covering the use of the class of p38 MAP kinase (mitogen-activated protein kinase) inhibitors for the treatment of severe influenza and hypercytokinaemia. The Company has also filed patent applications to expand its IP around POLB 001 and the use of p38 MAP kinase inhibitors in new disease areas, such as oncology. This enhances the value and attractiveness of POLB 001 to potential pharma partners.
New Risk • Aug 15New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of British stocks, typically moving 7.0% 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 Earnings are forecast to decline by an average of 14% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Less than 3 years of financial data is available. Currently unprofitable and not forecast to become profitable over next 2 years (UK£6.3m net loss in 2 years). Share price has been volatile over the past 3 months (7.0% average weekly change). Market cap is less than US$100m (UK£39.3m market cap, or US$50.0m).
お知らせ • Jun 30Poolbeg Pharma plc Announces Significant Breakthrough in Its World First Influenza Artificial Intelligence Programme with CytoreasonPoolbeg Pharma announced a significant breakthrough in its world first influenza Artificial Intelligence ('AI') Programme with CytoReason. Poolbeg has been working with CytoReason since March 2022. Poolbeg's unique disease progression data from influenza human challenge trials combined with CytoReason's broad repositories of curated disease data were analysed using CytoReason's AI-led platform. The analysis has led to the discovery of multiple novel drug targets for the treatment of influenza. Identification of drug targets from this unique data-set has previously been successful as p38 MAP Kinase, inhibited by POLB 001, was identified as a driver of severe influenza but this required manual analysis that took several years. However, through the utilisation of CytoReason's cutting-edge AI technology, Poolbeg has now identified multiple novel drug targets in just 15 months. Moreover, CytoReason's analysis independently confirmed the significance of the p38 MAP kinase pathway in influenza, providing further validation for Poolbeg's POLB 001 programme. The Company is actively exploring the most effective way to further develop the novel drug targets in order to generate value and looks forward to updating shareholders about the progress of this programme in due course. Poolbeg Pharma has access to a unique repository of clinical samples and associated data from human challenge trials. Data from human challenge trials are unique in that they track a healthy subject through disease to recovery in carefully controlled and monitored isolation units, collecting samples throughout the course of disease, and vitally collecting matched baseline and follow-up samples before and after infection. This data is unique in the depth of longitudinal virology, health, biomarker and symptom data collected during the course of disease.
Board Change • Jun 01Less than half of directors are independentFollowing the recent departure of a director, there are only 3 independent directors on the board. The company's board is composed of: 3 independent directors. 4 non-independent directors. Independent Non-Executive Director Patrick Ashe was the last independent director to join the board, commencing their role in 2021. The company's minority of independent directors is a risk according to the Simply Wall St Risk Model.
分析記事 • Jun 01We're Hopeful That Poolbeg Pharma (LON:POLB) Will Use Its Cash WiselyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, although...
お知らせ • May 24Poolbeg Pharma PLC Announces Board ChangesPoolbeg Pharma announced the appointment of Brendan Buckley as an Independent Non-Executive Director of the Company with immediate effect. Brendan will also replace Cathal Friel as a member of the Remuneration Committee. Professor Buckley is the former Chief Medical Officer of ICON plc, a medical graduate of University College Cork and a doctoral graduate in Biochemistry in the Faculty of Medicine at Oxford University. Prof Buckley has advised Poolbeg since inception and has deep experience in metabolic diseases including over 40 years' experience in clinical practice as a Consultant Physician in endocrinology, diabetes and in academic clinical pharmacology. Brendan was a member of the Board of Directors of the Irish Medicines Board (now the Health Products Regulatory Authority), chairing its statutory Advisory Committee for Human Medicines. He was also a member of the European Medicines Agency Committee for Orphan Medicinal Products (COMP) and of the European Medicines Agency Scientific Advisory Committee on diabetes and metabolism. Brendan has published over 150 scientific papers, mainly on metabolic disease, as well as the recent key opinion-leading book 'Re-Engineering Clinical Trials'. Mr. Brendan Mary Buckley, aged 73, has held the following directorships and/or partnerships in the past five years: Current directorships: hVIVO plc, FIGHTING BLINDNESS, DS BIOPHARMA LIMITED, Afimmune Limited, Open Orphan DAC, Imutex Ltd. Past directorships: BREAKTHROUGH CANCER RESEARCH and Alliance for Clinical Research Excellence and Safety Inc.
お知らせ • Jan 16Poolbeg Pharma plc Announces Strategic Expansion of Polb 001 into OncologyPoolbeg Pharma announces the strategic expansion of POLB 001 into oncology. While investigating the role of cytokine release syndrome ("CRS") in severe influenza, Poolbeg discovered data specific to the overt immune response in CAR T cell patients that suggest POLB 001 as a potential treatment option for this severe complication. The Company has submitted a patent application for the use of POLB 001 in addressing the impact of CRS in CAR T cell patients.CAR T cell therapies are a form of immunotherapy for cancer that have produced remarkable results across a range of haematological malignancies, including cases of complete and durable responses in patients with advanced leukaemia and lymphoma who failed on previous therapies. A significant number of patients suffer treatment related side effects, including CRS which in severe form can be life threatening. Cell therapies may induce these effects in up to 95% of patients1. Poolbeg has identified POLB 001 as a potentially valuable companion therapy to be used in conjunction with existing CAR T cell therapies to address this significant unmet need. POLB 001's mode of action, reducing hyperinflammation which is associated with CRS, has the potential to significantly reduce the serious adverse effects experienced by many CAR T cell patients. The filed patent application is expected to provide class protection for use of p38 inhibitors in CAR T cell treatment and opens up a significant new market opportunity for POLB 001 in addition to severe influenza. A long-term strategic objective for Poolbeg has been and continues to be to evaluate POLB 001's potential in additional indications to fully unlock the potential value of the molecule and strengthen Poolbeg's position with a view to potential partnering and out-licensing. The Company is performing oncology clinical trial enabling activities to progress towards trial initiation in CAR T cell patients in 2024. Further oncology-related data, regulatory feedback and non-clinical development updates are expected in 2023.
お知らせ • Jan 09Poolbeg Pharma PLC Announces Positive Initial Data Analysis in POLB 001 TrialPoolbeg Pharma PLC announced positive initial data analysis for POLB 001, a viral strain agnostic, small molecule immunomodulator being developed to address the significant unmet medical need for severe influenza. As announced in December, full data read-out is expected in Second Quarter 2023. However, upon initial review, the data indicates that administration of POLB 001 resulted in a marked reduction in both systemic and localised inflammatory response in subjects challenged with bacterial lipopolysaccharide ("LPS") compared to those who received placebo. A clear dose-response relationship was also apparent. This LPS challenge trial was designed to evaluate the effect of POLB 001 on inflammatory responses in 36 healthy volunteers between 18 and 55 years of age following both an intradermal and an intravenous LPS challenge. LPS acts as a surrogate for the hyperinflammatory response associated with severe influenza and other diseases. POLB 001 was well tolerated across all doses and no serious adverse events or volunteer withdrawals were reported.
分析記事 • Jul 12Here's Why We're Not Too Worried About Poolbeg Pharma's (LON:POLB) Cash Burn SituationEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
Board Change • Apr 27No 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. Member of Scientific Advisory Board Daniel Hoft was the last director to join the board, commencing their role in 2021. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.
お知らせ • Jul 20Poolbeg Pharma PLC has completed an IPO in the amount of £25 million.Poolbeg Pharma PLC has completed an IPO in the amount of £25 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 250,000,000 Price\Range: £0.1 Transaction Features: Regulation S
