Takeda Pharmaceutical filed an application seeking Japanese regulatory approval for an additional tablet formulation for the PARP inhibitor Zejula Capsules (niraparib) on November 26, the company said the same day. The Japanese drug giant licensed Zejula from US biotech Tesaro,…
To read the full story
Related Article
- Takeda Grabs Approval for Zejula Tablet Form
September 6, 2021
BUSINESS
- Chiba Downpours Cause No Major Disruption to Drug Operations
August 17, 2026
- Chugai Files Tecentriq for Colon Cancer Adjuvant Therapy in Japan
August 17, 2026
- Enflonsia Filed for High-Risk Children in 2nd RSV Season in Japan: MSD
August 17, 2026
- Sawai to Drop 46 Generic Products, Takata 30
August 17, 2026
- Healios to File MultiStem in Japan Without Waiting for PIII Results: CEO
August 17, 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.…





