Kaken Pharmaceutical said on May 15 that it has filed for regulatory approval in Japan for KP-001 (serabelisib), its investigational treatment for refractory vascular malformations. The application is based on data from a domestic PIII trial, with the company aiming…
To read the full story
Related Article
- Kaken’s KP-001 Hits Goal in PIII Vascular Malformation Trial
November 11, 2025
BUSINESS
- Kissei Urges Halt to New Tavneos Use after Fatal Liver Injury Reports
May 18, 2026
- Eisai Hits Record Sales as Leqembi Revenue Nearly Doubles in FY2025
May 18, 2026
- Kaken Files Vascular Malformation Drug in Japan, Eyes FY2027 Approval
May 18, 2026
- Regenxbio Appeals FDA CRL for MPS II Gene Therapy RGX-121
May 18, 2026
- Fuji Sees New Bio-AG Pricing Rules as Tailwind for Biosimilars
May 18, 2026
In the complex landscape of the Japanese pharmaceutical market, the “status quo” is often the safest harbor. But for leaders like Kennet Brysting, former president of Gilead Japan, the status quo is the most dangerous place to stay.Innovation in Japan…





