FDA
-
-
-
-
-
-
-
New clinical data on the Leqembi® subcutaneous autoinjector presented at AAIC® 2026 support similar efficacy and safety to IV formulation in early Alzheimer's disease
-
-
-
-
-
-
-
FDA extends Leqembi Iqlik review period to August 24
-
-
-
-
-
-
-
Sales of Leqembi® totaled 20.7 billion yen in the fourth quarter 2025
-
-
-
-
-
-
-
BioAge reports 86% reduction in inflammatory marker in Phase 1 trial
-
-
-
-
-
-
-
Leqembi® approved for IV maintenance treatment in the United Kingdom
-
-
-
-
-
-
-
BioAge Labs Reports Second Quarter 2025 Financial Results and Provides Business Updates
-
-
-
-
-
-
-
BioAge Labs completes IND-enabling studies for BGE-102, a potent, orally available, brain-penetrant NLRP3 inhibitor, and advances candidate toward the clinic
-
334,273 total articles have been posted to this entity.
Click Here to Sign-Up for StreetInsider.com Premium to View All


