oral infigratinib — NDA/BLA submission
Q4 2026
BridgeBio intends to submit a Marketing Authorization Application (MAA) for achondroplasia to the European Medicines Agency (E MA) in the fourth quarter of 2026.Source filing
catalyst calendar
BRIDGEBIO PHARMA INC · Data as of 2026-10-25
Q4 2026
BridgeBio intends to submit a Marketing Authorization Application (MAA) for achondroplasia to the European Medicines Agency (E MA) in the fourth quarter of 2026.Source filing
Nov 27
BBP-418 for limb-girdle muscular dystrophy type 2I/R9, or LGMD2I/R9 (PDUFA date with Priority Review: November 27, 2026);Source filing
2027
Submit IND to the FDA in 2027Source filing
Feb 4
The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of February 4, 2027, and BridgeBio is prepared to launch oral infigratinib upon approval.Source filing
May 7
encaleret for autosomal dominant hypocalcemia type 1, or ADH1 (PDUFA date with Priority Review: May 7, 2027);Source filing
Nov 6–Nov 9
More data on Attruby will be shared at the American Heart Association (AHA) Congress in November 2025 and in medical congresses throughout 2026.Source filing