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
- Shionogi Eyes Faster QOL Biz Expansion with Ex-JT Researchers: CEO
February 2, 2026
- Sumitomo Flags Diabetes Pipeline Gap as Key Strategic Issue: CEO
February 2, 2026
- Astellas, MSD Seek Japan Nod for Padcev/Keytruda in Perioperative MIBC
February 2, 2026
- Alfresa Launches End-to-End Platform to Support Biotech Entry into Japan
February 2, 2026
- Nichi-Iko’s Xarelto Generic Adds VTE Use
February 2, 2026
The Japanese healthcare sector is experiencing rapid growth, demanding a highly skilled and diverse workforce. However, finding and attracting the best talent in this competitive market presents significant challenges.Enter AI. With the rise of AI-powered tools, healthcare organizations can revolutionize…





