Otsuka Pharmaceutical said on January 27 that the US FDA has accepted its new drug application for centanafadine, an investigational treatment for attention-deficit hyperactivity disorder (ADHD), covering children, adolescents, and adults. The FDA has granted the application priority review, setting…
To read the full story
Related Article
- Otsuka Files Novel ADHD Drug Centanafadine in US
November 26, 2025
- Otsuka’s ADHD Med Hits Mark in PIII Pediatric Trials in US
October 30, 2023
- Otsuka’s ADHD Med Hits Primary Goal in US PIII Trials
June 15, 2020
- Otsuka to Buy Neurovance, Gets Its Hands on Non-Stimulant ADHD Med
March 6, 2017
BUSINESS
- J&J’s Tremfya Now Available for Self-Injection in IBD
June 2, 2026
- J&J Taps Leading Cancer Centers to Bolster Japan Trial Environment
June 2, 2026
- BMS Files Breyanzi for Relapsed/Refractory CLL, SLL in Japan
June 1, 2026
- Astellas Rebuts ISS Opposition to Outside Director Nominee
June 1, 2026
- Meiji Backs US Fund Supporting Pandemic Preparedness
June 1, 2026
In the complex landscape of the Japanese pharmaceutical market, the “status quo” is often the safest harbor. But for leaders like Kennet Brysting, former president of Gilead Japan, the status quo is the most dangerous place to stay.Innovation in Japan…





