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
- Santen Eyes Pterygium Drug as Key Pipeline Asset, 4 Million Potential Patients in Japan
March 23, 2026
- Chugai Files Device Component of Ranibizumab Eye Implant in Japan
March 23, 2026
- Shionogi’s Zurzuvae, Kissei’s Yselty Now Available in Japan
March 23, 2026
- Boehringer Files Hernexeos for First-Line NSCLC Use in Japan
March 23, 2026
- Novo Japan Logs 5.4% Growth in 2025, Sees Wegovy Powering Push for Double-Digit Goal
March 23, 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…





