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Curis Resumes Patient Enrolment in the Dose Escalation Study of Emavusertib for the Treatment of Leukemia

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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

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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