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FDA Approves New Dosing Option for CRYSVITA
®
(burosumab-twza) in Adults With XLH
FDA Approves New Dosing Option for CRYSVITA
®
(burosumab-twza) in Adults With XLH
May 14, 2026
Read more
Kura Oncology and Kyowa Kirin to Present Updated Frontline Ziftomenib / 7+3 Combination Data at EHA 2026 Congress
May 12, 2026
CRYSVITA
®
Now Publicly Reimbursed for the Treatment of Adults with XLH in Four Provinces and Federal Non-Insured Health Benefits Program
May 6, 2026
Kyowa Kirin Announces Discontinuation of Rocatinlimab Clinical Trials
March 3, 2026
Kyowa Kirin to Regain Control of Rocatinlimab Development and Commercialization Program, Demonstrating Strong Commitment to Address High Unmet Medical Need in Atopic Dermatitis
January 30, 2026
Kyowa Kirin Announces Proposed Appointment of Abdul Mullick to President and Chief Executive Officer, While Former CEO Masashi Miyamoto to Remain Chairman
December 11, 2025
Kura Oncology and Kyowa Kirin Report Combination Data for KOMZIFTI™ (Ziftomenib) with Venetoclax and Azacitidine in Newly Diagnosed and Relapsed/Refractory AML
December 8, 2025
KOMZIFTI™ (ziftomenib) Added to National Comprehensive Cancer Network
®
(NCCN) Guidelines for Acute Myeloid Leukemia (AML)
November 25, 2025
Kyowa Kirin to Present New Research Highlighting Mogamulizumab’s Clinical Utility and Strategic Potential in T-Cell Lymphomas at 2025 ASH Annual Meeting
November 18, 2025
Kura Oncology and Kyowa Kirin Announce FDA Approval of KOMZIFTI™ (ziftomenib), the First and Only Once-Daily Targeted Therapy for Adults with Relapsed or Refractory NPM1-Mutated Acute Myeloid Leukemia
November 13, 2025
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