Q2 2026 drug catalysts put Replimune, Arvinas and Boehringer in sharp focus: GlobalData
Key FDA decisions and pivotal late-stage obesity and breast cancer data could reshape competitive positioning
Key FDA decisions and pivotal late-stage obesity and breast cancer data could reshape competitive positioning
The acquisition brings two commercialized, differentiated medicines—EMPAVELI and SYFOVRE —to Biogen’s growth portfolio
The trial demonstrated that immune responses in children were non-inferior to adults, with a similar safety profile after two standard doses of MVA-BN
Beyond clinical trials, real-world evidence is adding weight to AbbVie’s claims
Since launching, the hospital has performed over 40 intestinal transplants, including 21 in 2025 alone
Capital infusion to accelerate Earendil’s R&D platform
The Macau authorization followed a regulatory review that considered prior decisions by both the US FDA) and the European Medicines Agency
The approval of Cosentyx represents an important advancement for younger HS patients who have had limited treatment options
Previously, Arexvy was authorized for adults 60 and older, and for those 50–59 with heightened risk
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