Takeda Pharmaceutical said on December 22 that the US FDA has issued a complete response letter (CRL) rejecting approval of its eosinophilic esophagitis treatment TAK-721 (budesonide oral suspension).The drug maker said that the FDA concluded that an application for the…
To read the full story
Related Article
- Takeda Earns US Nod for Oral EoE Drug after Resubmission
February 14, 2024
- FDA Accepts Takeda’s Resubmission for Eosinophilic Esophagitis Drug
September 22, 2023
- Takeda’s Eosinophilic Esophagitis Med Gets Priority Review in US
December 17, 2020
BUSINESS
- Sanofi Debuts Sarclisa SC, Cutting Dosing Time
August 28, 2026
- Daiichi Starts Global PIII of Datroway in Adjuvant Urothelial Cancer
August 28, 2026
- FDA Accepts Kowa’s Glaucoma Drug K-911 for Review
August 28, 2026
- Hokuriku Downpours Cripple Some Drug Deliveries; Wholesalers Report No Damage
August 28, 2026
- Shionogi, Susmed End Sales Partnership for Insomnia App
August 27, 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.…





