PHARMA JAPAN welcomes JETRO New York’s Shunsuke Tani as a guest columnist. In occasional contributions, Tani will share his perspectives on US pharmaceutical policy, industry developments, and life in America, drawing on his firsthand experience in the US.---Hello from New…
The US FDA has rejected the approval of vadadustat, a renal anemia treatment jointly developed by Akebia Therapeutics and Otsuka Pharmaceutical, citing safety concerns in a complete response letter (CRL) issued to the US drug maker on March 30. In…
To read the full story
Related Article
- Otsuka Ends Vadadustat Global License Deal with Akebia
May 16, 2022
- Otsuka Files HIF-PH Inhibitor Vadadustat in Europe
November 1, 2021
- FDA Target Date for Vadadustat Set for March 29: Otsuka/Akebia
June 2, 2021
- Otsuka Partner Akebia Files HIF-PH Inhibitor Vadadustat in US
March 31, 2021
- Akebia/Otsuka’s HIF-PH Inhibitor Vadadustat to Be Filed in US in Early 2021
September 7, 2020
- Akebia/Otsuka's Vadadustat Hits Primary Target in Multinational PIII
May 8, 2020
- Otsuka, Akebia Expand Licensing Pact for Anemia Med Vadadustat
April 27, 2017
- Otsuka, Akebia Form US Collaboration on Anemia Med Vadadustat
December 22, 2016
- Mitsubishi Tanabe Gains Exclusive Rights to Akebia’s Anemia Drug in Asia
December 16, 2015
BUSINESS
- Sumitomo’s Enzomenib Earns US Breakthrough Therapy Tag for Leukemia
October 28, 2026
- PDRadiopharma to Build 16.5 Billion Yen Plant in Chiba
October 28, 2026
- FRONTEO, Otsuka Tie Up on AI-Driven Kidney Drug Target Discovery
October 28, 2026
- Enhertu Reels in EU OK for Adjuvant Use in HER2 Breast Cancer
October 28, 2026
- Silchester Boosts Santen Stake Past 10%
October 28, 2026





