Regulatory MSD, Daiichi Sankyo’s ifinatamab deruxtecan receives FDA priority Pharmaceutical Business ReviewThe treatment targets adult patients with ES-SCLC who have experienced disease progression on or after platinum-based chemotherapy.RegulatoryOncologyRead full story pharminent April 14, 2026 (Last updated: April 14, 2026) Pharmaceutical Business Review The treatment targets adult patients with ES-SCLC who have experienced disease progression on or after platinum-based chemotherapy. RegulatoryOncologyRead full story Post navigation Previous: Travere claims first FDA OK in rare kidney disease FSGSNext: Travere Therapeutics gains FDA approval for sparsentan in FSGS Related Stories Regulatory Ultragenyx wins FDA approval for first treatment targeting root cause of GSDIa pharminent August 20, 2026 Regulatory Regeneron wins FDA approval to challenge Ipsen for rare bone disease market pharminent August 20, 2026 Regulatory FDA grants accelerated approval to Ultragenyx’s Genglycos gene therapy pharminent August 20, 2026
