New PROSPER Data Demonstrate Real-World Impact of Mogamulizumab on Symptoms and Health-Related Quality of Life in Mycosis Fungoides and Sézary Syndrome

June 29, 2026 08:30 ET  | Source: Kyowa Kirin PRINCETON, N.J., June 29, 2026 (GLOBE NEWSWIRE) — Kyowa Kirin, Inc., a wholly owned subsidiary of Kyowa Kirin Co. Ltd (TSE: 4151), today announced positive results from PROSPER, a real-world observational study of mogamulizumab in adults with mycosis fungoides (MF) or Sézary syndrome (SS). In the study, patients […]

Zymeworks to Acquire Theravance Biopharma, Inc.

June 29, 2026 06:00 ET  | Source: Zymeworks Inc. VANCOUVER, British Columbia, June 29, 2026 (GLOBE NEWSWIRE) — Zymeworks Inc. (Nasdaq: ZYME) (the “Company”), a biotechnology company managing a portfolio of licensed healthcare assets and developing a diverse pipeline of novel, multifunctional biotherapeutics, today announced it has entered into a definitive agreement to acquire Theravance Biopharma, Inc.

Evaluate Recognized for Artificial Intelligence Innovation in 9th Annual AI Breakthrough Awards Program

Ninth Annual Program Honors the AI Innovators Shaping the Next Era of Global Innovation June 25, 2026 09:00 ET  | Source: Evaluate LONDON, June 25, 2026 (GLOBE NEWSWIRE) — Evaluate, a Norstella company and the leading global provider of market insights for the pharmaceutical industry, today announced that Ask Ella has been named “Enterprise AI Search Solution of the Year”

SK pharmteco Announces SKyvec™, A Unified, High-Yield Viral Vector Platform Designed to Accelerate Gene Therapy Development from Batch to Bedside

June 23, 2026 09:03 ET  | Source: SK pharmteco Inc. RANCHO CORDOVA, Calif., June 23, 2026 (GLOBE NEWSWIRE) — SK pharmteco today announced the launch of SKyvec™, its proprietary, multimodal viral vector platform. Designed to support gene therapy programs at every stage, from early research through clinical supply and commercial manufacturing, the SKyvec™ platform integrates development capabilities with global

Evaluate Releases Annual World Preview Report Revealing Updated Market Forecasts for the Pharmaceutical Industry

The 2026 report highlights top drivers of global pharmaceutical sales, M&A, and China’s continued impact on the industry June 23, 2026 09:00 ET  | Source: Evaluate LONDON, June 23, 2026 (GLOBE NEWSWIRE) — Evaluate, the leading provider of market insights for the pharmaceutical industry, today released its 2026 World Preview Report, providing updated insights for the global pharmaceutical market.

Boehringer Ingelheim accelerates precision oncology research with initiation of three Phase III trials in hard-to-treat cancers

June 22, 2026 03:00 ET  | Source: Boehringer Ingelheim Limited Ingelheim, Germany and Ridgefield, Conn – Boehringer Ingelheim is advancing biomarker-informed approaches and extending precision care across multiple cancers and stages of disease, reinforcing its ambition to bring unprecedented impact and improve long-term outcomes where unmet need remains high.4,5,6 The company has initiated two Phase III clinical trials within

Avance Clinical Announces Asia Pacific and Mainland China Expansion Ahead of BIO International Convention 2026

Global CRO expands its operational footprint into Singapore and Malaysia, strengthens China presence, and grows India operations – creating a powerhouse in the Asia Pacific region June 19, 2026 06:30 ET  | Source: Avance Clinical ADELAIDE, Australia, June 19, 2026 (GLOBE NEWSWIRE) — Avance Clinical, the Australian-headquartered global Contract Research Organization (CRO) for biotechs, today announced a

Teva Releases Q2 2026 Aide Memoire

June 18, 2026 17:00 ET  | Source: Teva Pharmaceutical Industries Ltd TEL AVIV, Israel, June 18, 2026 (GLOBE NEWSWIRE) — Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) announced today that its Q2 2026 Aide Memoire is available on the “Investors” page on its website. Q2 2026 Aide Memoire Teva has compiled this document with public information

Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome

June 18, 2026 16:57 ET  | Source: Teva Pharmaceutical Industries Ltd TEL AVIV, Israel, June 18, 2026 (GLOBE NEWSWIRE) — Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a first-in-class investigational therapy for the treatment of pediatric

SK pharmteco Announces Strategic Collaboration with Orphan Therapeutics Accelerator for the Development and Manufacturing of Rare Disease Therapies

June 18, 2026 09:03 ET  | Source: SK pharmteco Inc. RANCHO CORDOVA, Calif., June 18, 2026 (GLOBE NEWSWIRE) — SK pharmteco today announced a collaborative agreement with the Orphan Therapeutics Accelerator (OTXL), a non-profit, biotech focused on completing development and enabling access to stalled rare disease treatments, to support the advancement of novel therapeutic programs. The strategic partnership is built on

Court victory paves the way for Curium’s plans to provide targeted radioligand therapy to U.S. patients with GEP-NETs

June 18, 2026 07:45 ET  | Source: Curium BOSTON, June 18, 2026 (GLOBE NEWSWIRE) — Curium™ is pleased to announce that it has prevailed in the patent dispute brought by Novartis subsidiary Advanced Accelerator Applications against Curium™ concerning Curium’s Lutetium Lu 177 dotatate product. In the court decision issued yesterday by the Delaware U.S. District Court, Justice

New analyses from FIBRONEER™ trials suggest survival benefit with nerandomilast in IPF and PPF

June 18, 2026 04:05 ET  | Source: Boehringer Ingelheim Limited Not intended for UK and US audiences  Ingelheim, Germany – Long-term survival modeling of Boehringer Ingelheim’s oral preferential PDE4B inhibitor, nerandomilast, predicts the therapy could extend survival by up to 5.4 years in adults with idiopathic pulmonary fibrosis (IPF) and up to 3.3 years in adults with progressive

Optimi Health Launches Standardized Microdose Psilocybin Products for Clinical Research

June 16, 2026 08:30 ET  | Source: Optimi Health Corp. Two naturally derived finished drug products, at 1mg and 2mg, give research organizations the consistent, validated doses required for controlled studies New microdose formats extend Optimi’s psilocybin range, which includes a 5mg formulation currently commercially prescribed for treatment-resistant depression in Australia under the country’s Authorized Prescriber Scheme

Scroll to Top