Takeda Pharmaceutical and Protagonist Therapeutics said on March 2 that the US FDA has accepted a new drug application for rusfertide, an investigational treatment for polycythemia vera (PV), under a priority review pathway. The FDA set a target action date…
To read the full story
Related Article
- Takeda Files Polycythemia Vera Drug Rusfertide in US
January 7, 2026
- Takeda on Course to Stable Growth as Late-Stage Assets Near Market
May 9, 2025
- Protagonist/Takeda’s Hematology Med Makes Mark in PIII
March 5, 2025
- Takeda Sees Up to US$20 Billion Sales Potential with 6 Late-Stage Assets
December 16, 2024
- Takeda Bags Global Rights to Protagonist’s Rare Hematology Asset
February 2, 2024
BUSINESS
- Sumitomo Regains Growth Momentum, Eyes 350 Billion Yen from 2 Key Drugs in FY2028
March 3, 2026
- Middle East Turmoil Raises Fears over API Shipments as Key Airports Shut
March 3, 2026
- Itochu Snaps Up CoreMed to Bolster Japan Entry Support
March 3, 2026
- Ono to Transfer Opalmon, Prostandin to Daito by November
March 3, 2026
- Epadel Launched in Vietnam: Mochida/Meiji
March 3, 2026
I recently sat down with one of the leading medical directors in Japan to discuss the critical evolution of the medical science liaison (MSL) role.The MSL has transformed from a scientific resource into a strategic partner essential for successful product…





