Curis Resumes Patient Enrolment in the Dose Escalation Study of Emavusertib for the Treatment of Leukemia
Shots:
- The US FDA placed a partial clinical hold on the TakeAim leukemia & lymphoma study on Apr’22 which has now been lifted after the review of the comprehensive data package submitted by the company to the US FDA
- The company will now resume patient enrolment of additional patients (n=6) in the P-Ia (TakeAim) leukemia study evaluating Emavusertib (200mg), an IRAK4 kinase inhibitor. The partial hold still remains intact on the P-Ib & expansion P-IIa study until the completion of the P-Ia study & approval by the US FDA to proceed to the next phase
- The US FDA reviewed the additional data based on the risk of rhabdomyolysis provided by Curis along with its strategy to utilize objective laboratory measurements to identify rhabdomyolysis
Ref: PR Newswire | Image: Curis
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