The US FDA has accepted for review a resubmission made by Takeda Pharmaceutical for its eosinophilic esophagitis (EoE) treatment TAK-721 (budesonide oral suspension), the company said on September 20. A decision from the regulator is expected in the first half…
To read the full story
Related Article
- Takeda Earns US Nod for Oral EoE Drug after Resubmission
February 14, 2024
- Takeda’s Eosinophilic Esophagitis Drug Rejected in US
December 23, 2021
- Takeda’s Eosinophilic Esophagitis Med Gets Priority Review in US
December 17, 2020
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…





