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CHMP recommends EU approval of Brinsupri (brensocatib) for the treatment of non-cystic fibrosis bronchiectasis – Insmed

Written by | 5 Nov 2025

Insmed announced that the Committee for Medicinal Products for Human Use (CHMP) of the EMA has adopted a positive opinion recommending approval of its DPP1 inhibitor Brinsupri (brensocatib… read more.

Teva and Prestige Biopharma enter license agreement for Tuznue (trastuzumab biosimilar) commercialization in Europe

Written by | 4 Nov 2025

Teva Pharmaceutical Industries Ltd. entered into a license agreement with Prestige Biopharma, for the commercialization of Tuznue (trastuzumab), a biosimilar to Herceptin, across a majority of European markets…. read more.

Xtandi (enzalutamide) plus leuprolide reduced risk of death by 40% vs leuprolide alone in men with a type of advanced prostate cancer – Pfizer

Written by | 3 Nov 2025

Pfizer Inc and Astellas announced final overall survival (OS) results from the Phase III EMBARK study evaluating Xtandi (enzalutamide), in combination with leuprolide and as monotherapy, in men with… read more.

KalVista to present late-breaking and poster data on sebetralstat at ACAAI 2025

Written by | 2 Nov 2025

KalVista Pharmaceuticals, Inc. announced the acceptance of one abstract for late-breaking oral presentation and three for poster presentation at the American College of Allergy, Asthma & Immunology (ACAAI) 2025 Annual… read more.

Jascayd (nerandomilast) approved in China for the treatment of idiopathic pulmonary fibrosis – Boehringer Ingelheim

Written by | 2 Nov 2025

Boehringer Ingelheim’s Jascayd (nerandomilast) has been approved by China’s National Medical Products Administration (NMPA) as an oral treatment option for idiopathic pulmonary fibrosis (IPF) in adult patients. This… read more.

Theravance Biopharma will share clinical insights on norepinephrine reuptake inhibitor ampreloxetine at AAS 2025

Written by | 1 Nov 2025

Theravance Biopharma, Inc announced that it will be participating at the 36th International Symposium on the Autonomic Nervous System, organized by the American Autonomic Society (AAS), taking place November 5-8, 2025, in Clearwater… read more.

FDA approves Gazyva/Gazyvaro (obinutuzumab) for the treatment of lupus nephritis – Roche

Written by | 1 Nov 2025

Roche announced  that the FDA  has approved Gazyva/Gazyvaro (obinutuzumab) for the treatment of adult patients with active lupus nephritis (LN) who are receiving standard therapy, as well as… read more.

Alexion to highlight advances across its rare neurology portfolio at AANEM and MGFA 2025

Written by | 31 Oct 2025

Alexion, AstraZeneca Rare Disease, will deliver 18 presentations, including four oral presentations, from its leading rare neurology portfolio at the American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM)… read more.

Agreement announced with U.S. Government to expand access to IVF-Therapies including Gonal-f, Ovidrel and Cetrotide – Merck

Written by | 31 Oct 2025

Merck KGaA announced that EMD Serono, their healthcare business of Merck in the U.S. and Canada, and U.S.-President Donald J. Trump’s administration entered into an agreement to expand… read more.

Leqembi IQLIK (lecanemab-irmb) subcutaneous autoinjector named as one of TIME’s “Best Inventions of 2025” – Eisai + Biogen

Written by | 30 Oct 2025

Eisai Co., Ltd. and Biogen Inc. announced that Leqembi IQLIK, a subcutaneous autoinjector formulation of lecanemab (generic name), for the treatment of Alzheimer’s disease (AD) has been selected… read more.

MetaVia will share clinical results for GPR119 agonist Vanoglipel at AASLD Liver Meeting 2025

Written by | 29 Oct 2025

MetaVia Inc a clinical-stage biotechnology company focused on transforming cardiometabolic diseases,  announced that an abstract highlighting data on Vanoglipel (DA-1241), a novel G-Protein-Coupled Receptor 119 (GPR119) agonist, has… read more.

Rinvoq (upadacitinib) demonstrated superiority versus Humira (adalimumab) for primary endpoint in a head-to-head study in rheumatoid arthritis patients who have failed first TNF Inhibitor – AbbVie

Written by | 29 Oct 2025

AbbVie announced positive topline results from the Phase IIIb/IV head-to-head SELECT-SWITCH study evaluating the efficacy and safety of upadacitinib (Rinvoq) 15 mg, once daily, compared to adalimumab (Humira)… read more.

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