Daiichi Sankyo said on June 26 that a key European advisory panel has recommended against approval of its cancer drug pexidartinib for the treatment of adult patients with symptomatic tenosynovial giant cell tumor (TGCT). The Japanese company submitted the drug…
To read the full story
Related Article
- Daiichi Sankyo’s Pexidartinib Bags 1st FDA Nod for Rare Joint Tumor
August 6, 2019
- Cancer Drug Pexidartinib Filed in Europe: Daiichi Sankyo
April 5, 2019
- Daiichi Sankyo’s Cancer Med Pexidartinib Gets Priority Review in US
February 7, 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…





