BUSINESS
FDA Accepts Nippon Shinyaku’s DMD Drug for Review, Target Date Set for Q3 2020
Nippon Shinyaku said on February 7 that the US FDA has accepted its oligonucleotide drug viltolarsen for priority review as a treatment of Duchenne muscular dystrophy (DMD), with a target action date set for the July-September quarter of 2020. The…
To read the full story
Related Article
- Nippon Shinyaku’s DMD Treatment Approved in US
August 17, 2020
- Nippon Shinyaku Submits Sakigake DMD Drug Viltolarsen in Japan, Could Be Approved by March
September 27, 2019
BUSINESS
- Novartis Japan Chief Urges Pro-Innovation Policies to Sustain Investments
April 21, 2026
- Samsca Generics Extend Label to ADPKD
April 21, 2026
- ASKA Ups Stake in MedChoice Parent to Deepen Philippines Tie-Up
April 21, 2026
- Nxera Bags US$10 Million Milestone from AbbVie in Neuro Collaboration
April 21, 2026
- Asahi Kasei Closes Aicuris Buy, Eyes US$500 Million Sales by 2030
April 21, 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…





