• Mashup Score: 0

    The FDA has granted permission for enrollment to resume in the monotherapy phase 1a portion of the phase 1/2 TakeAim Leukemia trial evaluating emavusertib in relapsed/refractory acute myeloid leukemia or high-risk myelodysplastic syndromes.

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    • The @US_FDA has granted permission for enrollment to resume in the monotherapy phase 1a portion of the phase 1/2 TakeAim Leukemia trial evaluating emavusertib in R/R AML or high-risk myelodysplastic syndromes. #mdsm https://t.co/I4JbfQp26h

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    Dan Pollyea, MD, MS, discussed the difficulties in developing new agents for the treatment of high-risk MDS, the objective of the ENHANCE trial, and the potential for other therapies to emerge in the treatment paradigm.

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    • Magrolimab represents a potential step forward in the treatment of patients with high-risk MDS, where the current standard of care of azacitidine or decitabine fails to generate significant responses. @DanPollyea @CUMedicalSchool #mdsm https://t.co/21UZCAjFX2 https://t.co/NR9OfZ3I5P

  • Mashup Score: 0

    Dan Pollyea, MD, MS, discussed the difficulties in developing new agents for the treatment of high-risk MDS, the objective of the ENHANCE trial, and the potential for other therapies to emerge in the treatment paradigm.

    Tweet Tweets with this article
    • Dan Pollyea, MD, MS, discussed the difficulties in developing new agents for the treatment of high-risk MDS, the objective of the ENHANCE trial, and the potential for other therapies to emerge in the treatment paradigm.@DanPollyea @CUMedicalSchool #mdsm https://t.co/x6y0eY5bZk