Takeda Pharmaceutical said on September 3 that it has obtained Japanese approval for an additional tablet version of its PARP inhibitor Zejula (niraparib), which has been available only in capsule form. A once-daily oral drug, Zejula’s capsule version was launched…
To read the full story
Related Article
- Takeda to Discontinue Zejula Capsules, Urges Switch to Tablet Version
October 12, 2022
- 2 mg Pen of Supply-Crippled Ozempic, 3rd Avastin Biosimilar Get Japan Listing
May 24, 2022
- Takeda Seeks Japan Nod for Zejula Tablet Form
November 27, 2020
BUSINESS
- PMP Returns Slam Drug Makers' Leading Products, Prazaxa Cut 45%: Jiho Poll
March 13, 2026
- Lilly to Invest Additional 20 Billion Yen in Japan's Seishin Plant
March 13, 2026
- Fujifilm Invests in Austria’s Valanx Biotech to Boost ADC Technology
March 13, 2026
- Merck, CDMO Cyto-Facto Join Hands on Cell and Gene Therapy
March 13, 2026
- Anti-PD-1 Agonist Antibody Enters PI in Australia for Autoimmune Diseases: Meiji
March 13, 2026
I recently sat down with one of the leading medical directors in Japan to discuss the critical evolution of the medical science liaison (MSL) role.The MSL has transformed from a scientific resource into a strategic partner essential for successful product…





