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Poolbeg Pharma PLC Announces Option Agreement to Acquire Orphan Drug Candidate

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Poolbeg Pharma PLC has announced an option agreement to acquire an orphan drug candidate for Behçet's Disease. The exclusive 12-month option agreement with Silk Road Therapeutics Inc is for a novel topical muco-adherent formulation of Pentoxifylline (tPTX) to treat oral ulcers in patients with Behçet's Disease. The drug has completed a successful Phase 2 trial, demonstrating superiority over the current standard of care. It has secured Orphan Drug Designation and Fast Track Designation from the FDA, positioning it for a potential 505(b)(2) approval pathway in the U.S.

Poolbeg Pharma PLC ha annunciato un accordo di opzione per acquisire un candidato farmaco orfano per la malattia di Behçet. L'accordo esclusivo, della durata di 12 mesi, con Silk Road Therapeutics Inc riguarda una nuova formulazione topica mucoaderente di Pentoxifillina (tPTX) per il trattamento di ulcere orali nei pazienti affetti da malattia di Behçet. Il farmaco ha completato con successo una sperimentazione di Fase 2, dimostrando una superiorità rispetto allo standard attuale di trattamento. Ha ottenuto la designazione di farmaco orfano e la procedura accelerata dalla FDA, posizionandolo per un possibile percorso di approvazione 505(b)(2) negli Stati Uniti.
Poolbeg Pharma PLC ha anunciado un acuerdo de opción para adquirir un candidato a medicamento huérfano para la enfermedad de Behçet. El acuerdo de opción exclusivo de 12 meses con Silk Road Therapeutics Inc es para una nueva formulación tópica mucoadhesiva de Pentoxifilina (tPTX) para tratar las úlceras orales en pacientes con enfermedad de Behçet. El medicamento ha completado con éxito un ensayo de fase 2, demostrando superioridad sobre el estándar de cuidado actual. Ha obtenido la designación de medicamento huérfano y la designación de vía rápida por parte de la FDA, posicionándolo para una posible ruta de aprobación 505(b)(2) en EE. UU.
Poolbeg Pharma PLC는 베체트병 치료를 위한 고아약 후보 물질의 옵션 계약을 발표하였습니다. 이 12개월 독점 옵션 계약은 Silk Road Therapeutics Inc와의 계약으로, 베체트병 환자의 구강 궤양 치료를 위한 새로운 국소 점착 형태의 펜톡시필린(tPTX)에 관한 것입니다. 이 약물은 성공적으로 2상 시험을 완료하여 현재의 표준 치료법보다 우수함을 입증하였으며, FDA로부터 고아 약물 지정과 신속 추진 지정을 획득하여 미국 내 505(b)(2) 승인 경로의 가능성을 자리매김하였습니다.
Poolbeg Pharma PLC a annoncé un accord d'option pour acquérir un candidat médicament orphelin pour la maladie de Behçet. L'accord d'option exclusif de 12 mois avec Silk Road Therapeutics Inc concerne une nouvelle formulation topique mucoadhésive de Pentoxifylline (tPTX) pour traiter les ulcères buccaux chez les patients atteints de la maladie de Behçet. Le médicament a achevé avec succès un essai de phase 2, démontrant sa supériorité par rapport au standard de soins actuel. Il a obtenu la désignation de médicament orphelin et la désignation de voie rapide de la FDA, le positionnant pour un possible chemin d'approbation 505(b)(2) aux États-Unis.
Poolbeg Pharma PLC hat eine Optionsvereinbarung zum Erwerb eines Waisenmedikament-Kandidaten für die Behcet-Krankheit bekanntgegeben. Die exklusive 12-monatige Optionsvereinbarung mit Silk Road Therapeutics Inc betrifft eine neuartige topische mukoadhäsive Formulierung von Pentoxifyllin (tPTX) zur Behandlung von oralen Ulzera bei Patienten mit Behcet-Krankheit. Das Medikament hat eine erfolgreiche Phase-2-Studie abgeschlossen, in der es sich als überlegen gegenüber der derzeitigen Standardbehandlung erwiesen hat. Es hat die Orphan-Drug-Zulassung und die Fast-Track-Zulassung der FDA erhalten, was es für einen möglichen 505(b)(2)-Zulassungsweg in den USA positioniert.
Positive
  • Successful completion of Phase 2 trial showing superiority over standard of care.

  • Secured Orphan Drug Designation and Fast Track Designation from the FDA.

  • Potential for a 505(b)(2) approval pathway in the U.S.

  • tPTX has demonstrated accelerated oral ulcer healing and decreased pain in Behçet's Disease patients.

Negative
  • Clear unmet medical need for an effective treatment, indicating the severity of Behçet's Disease.

  • Current standard of care is inadequate with safety concerns.

  • Challenges exist in the clinical approval pathway despite positive trial results.

Exclusive Option Agreement to Acquire Orphan Drug Candidate for Behçet's Disease

Novel therapeutic with Fast Track and Orphan Designation

LONDON, UK / ACCESSWIRE / April 30, 2024 / Poolbeg Pharma (AIM:POLB)(OTCQB:POLBF), 'Poolbeg' or the 'Company'), a biopharmaceutical company focussed on the development and commercialisation of innovative medicines targeting diseases with a high unmet medical need, announces that it has entered into an exclusive 12-month option agreement with Silk Road Therapeutics Inc, for a nominal fee, to acquire a novel topical muco-adherent formulation of Pentoxifylline (tPTX) for the treatment of oral ulcers in patient's suffering from Behçet's Disease.

Key Highlights
12-month option agreement with Silk Road Therapeutics to acquire novel topical muco-adherent formulation of Pentoxifylline (tPTX), a treatment for oral ulcers in patient's suffering from Behçet's Disease which currently has no cure

Phase 2 trial successfully completed, demonstrating superiority over standard of care

Secured Orphan Drug Designation and Fast Track Designation from the FDA

Positioned for a potential 505(b)(2) approval pathway in the U.S.

Poolbeg will continue due diligence throughout the term of the exclusive option agreement which will include engagement with Silk Road Therapeutics to ascertain the clinical approval pathway

There is a clear unmet medical need for an effective treatment for this rare disease, which has no cure. Behçet's Disease causes inflammation of blood vessels and tissues, resulting in debilitating symptoms, the most common being oral ulcers which impact essential functions like eating, drinking and speaking.[1] Patients also suffer from reduced psychosocial quality of life[2]. Current standard of care is inadequate with safety concerns and there is a clear need for alternative treatment options.

The topical formulation of PTX, a small molecule with broad anti-inflammatory activity, has successfully demonstrated accelerated oral ulcer healing and decreased pain compared to standard of care in patients with Behçet's Disease in a Phase 2 clinical trial.

The drug is positioned for a potential 505(b)(2) approval pathway in the U.S. which can result in a much less expensive and much faster route to approval and commercialisation. tPTX has successfully secured FDA Fast Track Designation, designed to expedite development and review of certain medicines. It has also received Orphan Drug Designation from the FDA, providing seven years of market exclusivity upon marketing authorisation.

Jeremy Skillington, PhD, Chief Executive Officer of Poolbeg Pharma, said: "The foundation of any pharma company is a strong pipeline of assets, and we believe that topical PTX could fit well into our pipeline alongside our other assets as we increase our focus on rare and orphan diseases.

"We are delighted to enter this exclusive option agreement with Silk Road Therapeutics and Dr Timothy Coté, whose extensive experience, including as Director of the FDA Office of Orphan Products Development, adds invaluable insights into the regulatory pathway and ultimate approval and commercialisation of the drug.

"tPTX has the potential to transform the lives of patients suffering from Behçet's Disease, who currently lack effective and safe long term treatment options. Under this exclusive option agreement, we will advance our due diligence process and engage with Silk Road Therapeutics to further understand the clinical pathway to approval, and we look forward to updating the market in due course."

Timothy R. Coté, M.D., M.P.H., Chief Executive Officer of Silk Road Therapeutics, said: "Poolbeg Pharma shares our commitment to advancing healthcare innovation to support rare disease patients. With Fast Track Designation and Orphan Drug Designation secured, topical PTX has the potential to swiftly reach patients and offer a potentially transformative solution for those suffering from Behçet's Disease."

Investor presentation
Poolbeg Pharma CEO, Jeremy Skillington, PhD, and CBO David Allmond, along with Dr Timothy Coté, CEO of Silk Road Therapeutics,will provide a live presentation via the Investor Meet Company platform on Tuesday 30 April 2024 at 6pm BST.

The presentation is open to analysts and investors, those who already follow Poolbeg on the Investor Meet Company platform will automatically be invited. Investors can sign up to Investor Meet for free and add Poolbeg Pharma plc to their company dashboard via: https://www.investormeetcompany.com/poolbeg-pharma-plc/register-investor

Enquiries

Poolbeg Pharma Plc

Jeremy Skillington, CEO

Ian O'Connell, CFO

+44 (0) 207 183 1499

Cavendish Capital Markets Ltd (Nominated Adviser & Joint Broker)

Geoff Nash, Charlie Beeson, Nigel Birks, Harriet Ward (ECM)

+44 (0) 207 220 0500

Singer Capital Markets (Joint Broker)

Phil Davies, Sam Butcher

+44 (0) 207 496 3000

J&E Davy (Joint Broker)

Anthony Farrell, Niall Gilchrist

+353 (0) 1 679 6363

Optimum Strategic Communications

Nick Bastin, Vici Rabbetts, Elena Bates

+44 (0) 208 078 4357

poolbeg@optimumcomms.com

About Behçet's Disease
Behçet's Disease is a rare condition that results in inflammation of the blood vessels and tissues. Inflammation across multiple parts of the body leads to diverse symptoms, the most prevalent being recurrent oral ulcers, in addition to genital ulcers and inflammation of the eye and skin lesions. It is not yet known what triggers the disease or causes it to persist. However, it is clear there is a significant immune component with some suggestions that exaggerated responses to pathogens and increased cytokine and chemokine production may play key roles in the disease.[3]

About Poolbeg Pharma
Poolbeg Pharma plc is committed to the development and commercialisation of innovative medicines targeting diseases with a high unmet medical need, with a growing emphasis on rare and orphan diseases. Its model focusses upon developing its exciting clinical assets and commercialising approved and marketed drugs to support the growth of the Company and the development of its robust pipeline of innovative products, thereby driving significant value creation.

Poolbeg is led by an experienced leadership team with a history of delivering significant shareholder value. The team has been strengthened by the appointment of three former members of the Amryt Pharma plc leadership team, with the intention of repeating Amryt's success and generating near term revenues.

Poolbeg's clinical programmes target large addressable markets including cancer immunotherapy-induced CRS, infectious disease, and metabolic conditions such as obesity with the development of an oral GLP-1R agonist. It uses a cost-effective development philosophy to generate high quality human data to support partnering and further development. Its AI-led infectious disease programmes analyse unique data from human challenge trials to identify clinically relevant drug targets and treatments, leading to faster development and greater commercial appeal.

For more information, please go to www.poolbegpharma.com or follow us on Twitter and LinkedIn @PoolbegPharma.

Forward-Looking Statements
This announcement may contain forward-looking statements and the words "expect", "anticipate", "intends", "plan", "estimate", "aim", "forecast", "project" and similar expressions (or their negative) identify certain of these forward-looking statements. The forward-looking statements in this announcement are based on numerous assumptions and Poolbeg's present and future business strategies and the environment in which Poolbeg expects to operate in the future. Forward-looking statements involve inherent known and unknown risks, uncertainties and contingencies because they relate to events and depend on circumstances that may or may not occur in the future and may cause the actual results, performance or achievements to be materially different from those expressed or implied by such forward-looking statements. These statements are not guarantees of future performance or the ability to identify and consummate investments. Many of these risks and uncertainties relate to factors that are beyond Poolbeg's ability to control or estimate precisely, such as future market conditions, currency fluctuations, the behaviour of other market participants, the outcome of clinical trials, the actions of regulators and other factors such as Poolbeg's ability to obtain financing, changes in the political, social and regulatory framework in which Poolbeg operates or in economic, technological or consumer trends or conditions. Past performance should not be taken as an indication or guarantee of future results, and no representation or warranty, express or implied, is made regarding future performance. No person is under any obligation to update or keep current the information contained in this announcement or to provide the recipient of it with access to any additional relevant information.

[1] Hatemi G, Yurttas B, Kutlubay Z, Cote T, Derkunt S, Yazici Y, Yazici H. Pentoxifylline Gel for Oral Ulcers in Patients with Behçet's Syndrome [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/pentoxifylline-gel-for-oral-ulcers-in-patients-with-behcets-syndrome/. Accessed April 17, 2024.

[2] Ali S, Nagieb CS, Fayed HL. Effect of Behcet's disease-associated oral ulcers on oral health related quality of life. Spec Care Dentist. 2023 Jul-Aug;43(4):435-442. doi: 10.1111/scd.12782. Epub 2022 Sep 20. PMID: 36127751.

[3] behcetsuk.org

This information is provided by RNS, the news service of the London Stock Exchange. RNS is approved by the Financial Conduct Authority to act as a Primary Information Provider in the United Kingdom. Terms and conditions relating to the use and distribution of this information may apply. For further information, please contact rns@lseg.com or visit www.rns.com.

SOURCE: Poolbeg Pharma PLC



View the original press release on accesswire.com

FAQ

What is the drug being acquired by Poolbeg Pharma for Behçet's Disease?

Poolbeg Pharma is acquiring a novel topical muco-adherent formulation of Pentoxifylline (tPTX) for the treatment of oral ulcers in patients with Behçet's Disease.

What designations has the drug secured from the FDA?

The drug has secured Orphan Drug Designation and Fast Track Designation from the FDA.

What is the potential approval pathway for the drug in the U.S.?

The drug is positioned for a potential 505(b)(2) approval pathway in the U.S.

What symptoms of Behçet's Disease does the drug target?

The drug targets oral ulcers in patients suffering from Behçet's Disease.

Who is the CEO of Poolbeg Pharma?

Jeremy Skillington, PhD, is the Chief Executive Officer of Poolbeg Pharma.

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