Takeda Pharmaceutical said on October 8 that the US FDA’s advisory committee has given its thumbs-up to maribavir for the treatment of post-transplant recipients with cytomegalovirus (CMV) infection and disease refractory to treatment with or without resistance. The FDA’s Antimicrobial…
To read the full story
Related Article
- Takeda Files CMV Drug Maribavir in Japan
November 20, 2023
- Takeda’s CMV Drug Livtencity Bags US Approval
November 25, 2021
- Takeda’s CMV Drug Maribavir Gets FDA’s Priority Review
May 24, 2021
- Maribavir Hits Primary Goal for Post-Transplant CMV Infection: Takeda
December 8, 2020
BUSINESS
- Eisai to Raise 50 Billion Yen via Bond Issue for R&D, Licensing
June 5, 2026
- Japan Market for Fertility, Contraception, Female Disorders Put at 228.5 Billion Yen by FY2035
June 5, 2026
- Toho, DHL Partner on Healthcare Logistics Platform
June 5, 2026
- Keytruda Maintains Lead as Japan’s Top-Selling Drug for 32nd Month: Encise
June 5, 2026
- Boehringer’s Japan Pharma Sales Up for 7th Straight Year, 10-Plus Launches Eyed by 2030
June 4, 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…





