Takeda Pharmaceutical said on October 2 that it will voluntarily withdraw the accelerated approval granted from the US FDA for its lung cancer treatment Exkivity (mobocertinib) after the drug failed in a confirmatory trial. The Japanese juggernaut said that following…
To read the full story
Related Article
- Takeda’s Exkivity Approved in China for EGFR Exon 20+ NSCLC
January 16, 2023
- Takeda’s Exkivity Gets US Nod for EGFR Exon 20-Mutant NSCLC
September 17, 2021
BUSINESS
- Hisamitsu Starts Promotion of Yaz AGs under Bayer Alliance
March 11, 2026
- Seagen ADC Patent Dispute Ends with Daiichi Sankyo Victory
March 11, 2026
- Seikagaku Re-Files Herniated Disk Drug with US FDA
March 11, 2026
- Lotte to Step Up CVC Investments to Drive CDMO Synergies
March 10, 2026
- Ipsen to Withdraw Tazverik Overseas over Secondary Cancer Risk
March 10, 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…





