Aptevo Stock Gains on Encouraging Single-Agent Activity for APVO436 In Leukemia Patients

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  • Aptevo Therapeutics Inc APVO has announced positive results from Phase 1 dose-escalation trial evaluating lead ADAPTIR candidate, APVO436, for acute myeloid leukemia and myelodysplastic syndromes (AML/MDS).
  • The study met its primary endpoint of identification of an active dose level for advanced studies.
  • The Company plans to submit the data for publication later this year.
  • Of seven evaluable relapsed AML patients treated in Cohort 6, four showed stabilization of their leukemias.
  • Of those four patients with disease stabilization, three patients lived over 246 days, over 261 days, and over 281 days, respectively, and one progressed after a month.
  • Two relapsed AML patients, who experienced stabilization of their leukemia, achieved partial remission and subsequently a complete remission.
  • No partial or complete remissions have been observed at APVO436 dose levels either lower or higher than the Cohort 6 dose level.
  • APVO436 was generally well tolerated and demonstrated a favorable side effect profile, including the absence of severe or prolonged neutropenia, an often serious condition associated with CD123-targeting therapies.
  • Price Action: APVO shares are up 9.7% at $27.71 during the market session on the last check Wednesday.
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Posted In: BiotechNewsHealth CareGeneralBriefsleukemia
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