Takeda Pharmaceutical said on December 4 that its investigational agent maribavir (TAK-620) met the primary target in an overseas PIII study for the treatment of transplant recipients with refractory/resistant cytomegalovirus (CMV) infection. In the SOLSTICE trial, which was conducted in…
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 Earns FDA AdCom Backing
October 11, 2021
- Takeda’s CMV Drug Maribavir Gets FDA’s Priority Review
May 24, 2021
BUSINESS
- Takeda CEO Says Orzeyful Could Redefine NT1 Standard of Care
July 31, 2026
- Pfizer Seeks Pediatric Expansion for Hympavzi in Japan
July 31, 2026
- Nippon Shinyaku Exercises Option for AB2 Bio’s Tadekinig Alfa in US
July 31, 2026
- Alfresa Takes Stake in Ember to Bolster Pharma Cold Chain in Japan
July 31, 2026
- Sanwa Kagaku Says Kumamoto Plant Remains Shut, Drug Supplies Stable
July 31, 2026
A few weeks ago, I had coffee with a very talented executive. Let’s call him Kenji. He has a great job, a big salary, and a solid team. But he was unhappy. He felt bored and wanted a new challenge.…





