Analysis of individual placements across 43 companies over the past 18 months paints a vivid picture of Japan’s evolving healthcare industry. This comprehensive snapshot illuminates current market demands, strategic shifts, and the enduring appeal of this pivotal Asian market.Rare Diseases…
Kyowa Kirin said on November 5 that European regulators have accepted for review its application seeking an expanded indication for anti-FGF23 monoclonal IgG1 antibody Crysvita (burosumab) for the treatment of X-linked hypophosphatemia (XLH) in adults. The drug was granted conditional…
To read the full story
Related Article
- Crysvita Approved in Europe for Adult XLH: Kyowa Kirin
October 6, 2020
- EU Panel Backs Kyowa Kirin’s Crysvita for Adult XLH
July 28, 2020
- Kyowa Kirin’s Burosumab Earns Conditional Approval in Europe
February 27, 2018
BUSINESS
- Daiichi Sankyo H1 Revenue Zooms 20% as ADCs Drive Growth
November 2, 2026
- Meiji Pharma Wins Defamation Suit over Kostaive Remarks
November 2, 2026
- Senju Licenses Late-Stage CRAO Drug to Kiora in Ex-Asia Deal
November 2, 2026
- Towa Pushes Back Tanabe Factory Buyout by One Month
November 2, 2026
- Fatal Drug Mix-Up Prompts Safety Alert on Two Amphotericin B Products
November 2, 2026





