Ascentage Pharma Reports the US FDA’s Clearance to Commence the P-III Study of Olverembatinib for Chronic-Phase Chronic Myeloid Leukemia
Shots:
- The US FDA has granted clearance to Ascentage Pharma for commencing a global registrational P-III study of olverembatinib (HQP1351) in H1’24
- The open-label, randomized, registrational P-III study aims to evaluate the safety and efficacy of olverembatinib for the treatment of patients with CML-CP with/without T315I mutation
- Olverembatinib (approved in the Chinese mainland) is a third-generation BCR-ABL inhibitor that targets BCR-ABL and a range of BCR-ABL mutants incl. the T315I mutation
Ref: Ascentage Pharma | Image: Ascentage Pharma
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Shivani was a content writer at PharmaShots. She has a keen interest in recent innovations in the life sciences industry. She was covering news related to Product approvals, clinical trial results, and updates. We can be contacted at connect@pharmashots.com.
