The approval of Aβ-clearing antibodies like Leqembi (lecanemab) and Kisunla (donanemab) marked a landmark shift toward disease-modifying therapies in Alzheimer’s,…
BUSINESS
Takeda Files MAA for Alogliptin in Europe
Takeda Pharmaceutical announced on May 24 that its European subsidiary Takeda Global Research & Development Centre (Europe) (TGRD Europe) filed a marketing authorization application (MAA) for its dipeptidyl peptidase-4 (DPP-4) inhibitor SYR-322 (alogliptin; brand name in Japan: Nesina) with the…
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PHARMA JAPAN welcomes JETRO New York’s Shunsuke Tani as a guest columnist. In occasional contributions, Tani will share his perspectives on US pharmaceutical policy, industry developments, and life in America, drawing on his firsthand experience in the US.---Hello from New…
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