BUSINESS
EMA Accepts Astellas’ AML Drug Xospata for Review, Approval Could Come This Summer
Astellas Pharma said on February 28 that the European Medicines Agency has accepted for review a marketing authorization application for its acute myeloid leukemia (AML) treatment Xospata (gilteritinib). With the drug put on the agency’s accelerated path, it could land…
To read the full story
Related Article
- With European OK, Astellas’ Xospata Extends Lead over Daiichi Sankyo’s FLT3 Rival
October 28, 2019
- Astellas’ AML Drug Gets European Panel Backing
September 25, 2019
BUSINESS
- Leqembi FY2025 Global Sales Reach 88 Billion Yen: Eisai
May 1, 2026
- Rohto Files CMV Corneal Endotheliitis Drug in Japan
May 1, 2026
- Mochida Files in Japan for PAH Drug Tyvaso DPI
May 1, 2026
- Tanabe Clinches EU Approval for Parkinson’s Drug Onerji
May 1, 2026
- 3D “Deeply Disappointed” by Toho Plan to Seek Defense Trigger Approval
May 1, 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…





