Actinium Pharmaceuticals Announces First Patient Treated in Third and Final Dose Cohort of Actimab-A CLAG-M Combination Phase 1 Trial in Acute Myeloid Leukemia

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Mar 05, 2020
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- 86% complete remission rate with 71% of patients achieving negative minimal residual disease status with a sub-therapeutic dose of Actimab-A with CLAG-M in second dose cohort of early stage safety trial

- Preliminary remission rates achieved with Actimab-A combined with CLAG-M compare favorably to targeted agents recently approved for patients with relapsed or refractory AML

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