Communiqués PureTech Health plc

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Recherche biotechnologique et médicale

Marché Fermé - 17:35:05 21/08/2026 Varia. 5j. Varia. 1 janv.
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Communiqués

13/07 Celea Therapeutics Doses First Patient in Global Phase 3 SURPASS-IPF Trial Evaluating Deupirfenidone for the Treatment of Idiopathic Pulmonary Fibrosis AQ
13/07 PureTech Founded Entity Celea Therapeutics Doses First Patient in Global Phase 3 SURPASS-IPF Trial Evaluating Deupirfenidone for the Treatment of Idiopathic Pulmonary Fibrosis (IPF) BU
02/07 Celea Therapeutics Announces $180 Million Financing to Advance Deupirfenidone as a Potential New Standard of Care to Treat Idiopathic Pulmonary Fibrosis (IPF) BU
02/07 PureTech Founded Entity Celea Therapeutics Completes $180 Million Financing to Advance Deupirfenidone as a Potential New Standard of Care to Treat Idiopathic Pulmonary Fibrosis (IPF) BU
10/06 PureTech Health: Results of Annual General Meeting BU
09/06 PureTech Founded Entity Seaport Therapeutics Reports Positive Multiple-Ascending Dose Data from Phase 1 Proof-of-Concept Trial of GlyphAgo™ in Healthy Volunteers BU
13/05 PureTech to Showcase Deupirfenidone Program at the American Thoracic Society International Conference BU
29/04 PureTech Health : 2025 Annual Report and Accounts (optimized for printing) PU
29/04 PureTech Health : Notice of Meeting for 2026 AGM PU
29/04 PureTech Health : Proxy Form for 2026 AGM PU
29/04 PureTech Health : Notice of Annual General Meeting and Explanatory Circular to Shareholders 2026 PU
29/04 PureTech Health : Form of Proxy – Annual General Meeting 2026 PU
29/04 PureTech Health : 2025 Annual Report and Accounts (optimized for display) PU
29/04 PureTech Announces Annual Results for Year Ended December 31, 2025 BU
29/04 PureTech Announces Intention to Voluntarily Delist American Depositary Shares from Nasdaq and Concentrate Trading on the London Stock Exchange BU
27/04 PureTech Founded Entity Seaport Therapeutics Adds Intra-Cellular Therapies Founder and CEO, Dr. Sharon Mates, to its Board of Directors BU
23/04 PureTech Reports Positive Topline Data from Phase 1b Trial of LYT-200 in Relapsed, Refractory High-Risk Myelodysplastic Syndrome and R/R Acute Myeloid Leukemia AQ
22/04 PureTech Reports Positive Topline Data from Phase 1b Trial of LYT-200 in Relapsed/Refractory (R/R) High-Risk (HR) Myelodysplastic Syndrome (MDS) and R/R Acute Myeloid Leukemia (AML) BU
13/04 PureTech Health: Notice of Results BU
02/04 PureTech Announces Publication of Phase 2b ELEVATE IPF Trial Results in The American Journal of Respiratory and Critical Care Medicine BU
02/04 PureTech Founded Entity Seaport Therapeutics Announces Positive Proof of Concept Topline Results from Ongoing Phase 1 Trial of GlyphAgo™ in Healthy Volunteers BU
26/03 PureTech Founded Entity Seaport Therapeutics Announces Publication in Science Translational Medicine Featuring GlyphAllo (SPT-300) AQ
25/03 PureTech Founded Entity Seaport Therapeutics Announces Publication in Science Translational Medicine Featuring GlyphAllo™ (SPT-300) as the First Triglyceride-Mimetic Prodrug to Achieve Therapeutically Relevant Drug Levels in Humans BU
25/02 PureTech to Present at the Leerink Partners Global Healthcare Conference BU
19/02 PureTech Announces Orphan Drug Designations Granted by the U.S. Food and Drug Administration and European Commission for Deupirfenidone (LYT-100) in Idiopathic Pulmonary Fibrosis BU
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