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NEW YORK, NY, USA and MAINZ, GERMANY I May 28, 2025 I Pfizer Inc. (NYSE: PFE, “Pfizer”) and BioNTech SE (Nasdaq: BNTX, “BioNTech”) today announced that they ...
Zymeworks' collaborator BeOne Medicines secured the approval under the terms of their Asia-Pacific licence and partnership ...
2d
Pharmaceutical Technology on MSNAlvotech and Advanz to commercialise biosimilars in EuropeThe agreement encompasses development and commercial milestones for the products, which could amount to up to $180m.
Kennedy Jr. revoked the Centers for Disease Control and Prevention’s recommendation that healthy children and healthy pregnant women be vaccinated for COVID-19, leaving some experts concerned and ...
(Alliance News) - Nuformix PLC on Thursday said its lead programme, NXP002, has been granted orphan drug designation by the European Medicines Agency for the treatment of idiopathic pulmonary fibrosis ...
4d
MyChesCo on MSNOcugen Receives Rare Pediatric Disease Designation for OCU410STMALVERN, PA — Ocugen, Inc. (NASDAQ: OCGN) has announced that the U.S. Food and Drug Administration (FDA) has granted Rare ...
Since the European Medicines Agency (EMA) approval of omalizumab in 2005 as the first ever biologic for severe asthma, the ...
The administration of US President Donald Trump has taken a series of actions since January, 2025 that directly threaten the ...
Rocket Pharmaceuticals acknowledged the death of a patient in a pivotal trial assessing its Danon disease gene therapy candidate RP-A501, a study that the FDA has placed on clinical hold.
NEW YORK – The European Medicines Agency's Committee for Medicinal Products for Human Use recommended approval of Autolus Therapeutics' autologous CD19-directed CAR T-cell therapy Aucatzyl ...
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