Roche’s Perjeta regimen secures FDA priority review in breast cancer
The FDA’s decision on approval is anticipated to be taken by 28 January 2018. Roche’s supplemental Biologics License Application (sBLA), which was accepted by the FDA, is based
Bristol Myers Squibb (BMS) has reported full-year 2025 revenues of $48.2bn, essentially flat compared with $48.3bn in 2024.
"Novartis pioneers new therapeutic paradigms, creating definitive medicines for life-threatening diseases," said Jay Bradner, President of the Novartis Institutes for BioMedical Research. "Our Berkeley alliance powerfully extends our
“This alliance aims to define patients with solid tumors who may benefit from immunotherapy and to develop therapy resistance strategies,” said Aung Naing, M.D., associate professor of Investigational
The New York-based biopharmaceutical company said that the preliminary results were observed from the first six subjects enrolled in the open-label trial dubbed NCT02226146. Immune Pharmaceuticals stated that
Jacobs was selected for this project phase following the successful completion of the conceptual study and basic engineering design As Ferring Pharmaceuticals’ principal biopharmaceutical product development center, this
Bevespi Aerosphere showed a significant improvement in lung function as measured by trough forced expiratory volume in one second (FEV1), compared to its monotherapy components (glycopyrronium 14.4 µg