Hourly refreshTue, Oct 27, 2026

Press Release Database

Recent press releases, indexed by topic.
Topic

Biotech & pharma

2,246 press releases in English indexed under biotech & pharma.

Clear all filters
Keywords, dates and language
Sources
up to 10
Newswires (50)
Company newsrooms (91)
Companies
Releases linked to any of up to 10 companies
AllFinanceCryptoAISaaSHealthcareReal estateEnergyRetailAutomotiveGamingMediaEducation
+ 33 more topics
DownloadExcelTXT
Finance · SaaS

GT Biopharma to Host Live Company Presentation on the Development of TriKE® Platform for Cancer Treatment, September 11, 2026

SAN FRANCISCO, CALIFORNIA, Sept. 11, 2026 -- GT Biopharma, Inc. (the “Company”) (NASDAQ: GTBP), a clinical stage immuno-oncology company focused on developing innovative therapeutics based on the Company's proprietary TriKE® natural killer (NK) cell engager platform, will host a live company presentation on the development of the TriKE® platform for cancer treatment today, September 11, 2026, at 2:00 p.m. Eastern Time.

Sep 11 · 12:00GlobeNewswire
Finance · Healthcare

Allarity Therapeutics Announces Strategic Capital Allocation for Filing of SPAC Registration Statement

TARPON SPRINGS, Fla., September 11, 2026 – Allarity Therapeutics, Inc. (“Allarity” or the “Company”) (NASDAQ: ALLR), a Phase 2 clinical-stage pharmaceutical company dedicated to developing stenoparib—a differentiated dual PARP/Wnt pathway inhibitor using its proprietary DRP® technology, announced that Allarity Acquisition Corp., a newly formed special purpose acquisition company (SPAC), has publicly filed a Registrat

Sep 11 · 12:00GlobeNewswire
Finance · Biotech & pharma

Eloxx Pharmaceuticals Announces First Patients Dosed in Phase 2b EXACT Study of Exaluren in Nonsense Mutation Alport Syndrome

First two patients dosed in the EXACT study Topline data from the initial 16-week placebo-controlled portion of the study expected mid-2027; final readout expected by the end of 2027 ARLINGTON, Mass., Sept. 11, 2026 -- Eloxx Pharmaceuticals, Inc. (Nasdaq: ELOX), a...

Sep 11 · 11:30PR Newswire
Healthcare · Biotech & pharma

Frost & Sullivan presents the "GLOBAL GENE THERAPY CRDMO TECHNOLOGY INNOVATION LEADERSHIP AWARD" to PackGene Biotech Inc.

Shanghai, China--(September 11, 2026) - On August 4, the 20th Frost & Sullivan Global Growth, Innovation and Leadership (GIL) Summit and the 5th New Investment Event (the "2026 Frost & Sullivan New Investment Event") officially opened at Jing An Shangri-La, Shanghai.In conjunction with the Summit, the Celebratory Banquet for the 65ᵗʰ Anniversary of Frost & Sullivan Global and the 20ᵗʰ Anniversary of the GIL Summit in China was held, where the 2026 Frost & Sullivan Global Awards...

Sep 11 · 11:28Newsfile
Biotech & pharma

Nanoscope Therapeutics to Participate in the 28th Annual H.C. Wainwright Global Investment Conference

Sulagna Bhattacharya, Chief Executive Officer, to deliver corporate presentation on Monday, September 14, 2026 NEW YORK, Sept. 11, 2026 -- New York, September 11, 2026 — Nanoscope Therapeutics, Inc., a biotechnology company committed to developing and commercializing novel,...

Sep 11 · 11:07PR Newswire
Healthcare · Biotech & pharma

Pharmaceutical Regulatory Affairs in Asia Online Training Set for March 3–5, 2027 — Registration Now Open

Evolving Asian pharma regulations are driving demand for expertise in market entry, clinical trials, product registration and lifecycle compliance for innovative drugs and generics. Evolving Asian pharma regulations are driving demand for expertise in market entry, clinical trials, product registration and lifecycle compliance for innovative drugs and generics.

Sep 11 · 09:13GlobeNewswire
Biotech & pharma

A Practical Approach to Veterinary Vaccine Development and Registration in the EU Sets March 2027 Online Training Date

Rising demand for veterinary biologics creates opportunities for vaccine development expertise and practical EU market authorization training. Rising demand for veterinary biologics creates opportunities for vaccine development expertise and practical EU market authorization training.

Sep 11 · 09:06GlobeNewswire
AI · Healthcare

Patient-Derived Xenograft/PDX Model Market - Global Forecast 2026-2032

Opportunities include integrated PDX platforms, humanized models, organoid pairing, AI analytics, annotated biobanks, precision oncology, and expansion across emerging research hubs. Opportunities include integrated PDX platforms, humanized models, organoid pairing, AI analytics, annotated biobanks, precision oncology, and expansion across emerging research hubs.

Sep 11 · 08:50GlobeNewswire
Healthcare · Biotech & pharma

The U.S. FDA grants orphan drug designation for Lundbeck's investigational anti-ACTH monoclonal antibody asedebart for treatment of endogenous Cushing's syndrome

The U.S. FDA has granted Orphan Drug Designation for asedebart (Lu AG13909), Lundbeck's novel investigational anti-ACTH monoclonal antibody, for the treatment of endogenous Cushing's syndrome Endogenous Cushing's Syndrome is a rare endocrine disorder driven in most cases by excess...

Sep 11 · 08:24PR Newswire
Finance · Biotech & pharma

Capricor Therapeutics, Inc. Sued for Securities Law Violations - Contact the DJS Law Group to Discuss Your Rights - CAPR

LOS ANGELES, Sept. 11, 2026 -- The DJS Law Group reminds investors of a class action lawsuit against Capricor Therapeutics, Inc. ("Capricor" or "the Company") (NASDAQ: CAPR) for violations of §§10(b) and 20(a) of the Securities Exchange Act of 1934 and Rule 10b-5 promulgated...

Sep 11 · 08:18PR Newswire
Healthcare · Biotech & pharma

Persica Pharmaceuticals publishes new analysis of assay sensitivity in disc microbiology studies, reinforcing the potential for PP353 in vertebrogenic Lumbar Back Pain

London, UK, 11 September 2026 - Persica Pharmaceuticals Limited (“Persica”), a clinical-stage biotechnology company developing PP353, a targeted, non-opioid treatment for vertebrogenic Lumbar Back Pain (vLBP), today announced publication of a new analysis examining why previous disc microbiology studies have reported divergent findings on bacterial presence in spinal discs.

Sep 11 · 06:00GlobeNewswire
Healthcare · Food & drink

Nicox Announces NCX 470 NDA in China Accepted for Review

1 A PDUFA date is the target date by which the U.S. Food and Drug Administration (FDA) aims to complete its review and issue a decision on a New Drug Application (NDA) under the Prescription Drug User Fee Act (PDUFA).

Sep 11 · 05:30GlobeNewswire