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A drug, AB8939, alone and in combination with venetoclax, to treat acute myeloid leukemia (AML) that has come back (relapsed) or not gotten better with treatment (refractory)

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18 and older

Phase 1, Phase 2

1 Location

NCT05211570

Clinical Trial Goal


To find out:
  • The highest dose of AB8939 that's safe to give 
  • If AB8939 is safe and works well to treat AML that has relapsed or is refractory

You may be able to join this trial if you:


  • Are 18 years or older
  • Have AML that has relapsed or is refractory
  • Do not have acute promyelocytic leukemia
  • Are not eligible for an autologous (your own cells) or an allogeneic (cells from a donor) blood or marrow transplant (BMT)
  • Are not eligible for standard treatment options
  • Agree to have other standard tests done to see if you can be in the clinical trial 

Trial Details


AB8939 is a small molecule synthesized tubulin inhibitor. 
Venetoclax is a small molecule inhibitor that blocks BCL2 in certain cells.

You'll get:
  • AB8939 – Given as intravenous (IV) infusions . The dose you'll get depends on when you start the trial and how safe it has been
  • Venetoclax –  A pill that you take by mouth. The dose you'll get depends on when you start the trial and how safe it has been

You'll have biopsies to see how well the treatment is working. The clinical trial doctors will check your health for about 2 months.

The Food and Drug Administration (FDA) has  not yet approved AB8939. 

Contacts


Clinical Study Coordinator, +33(0)147200014, clinical@ab-science.com

Locations


MD Anderson Cancer CenterNOT_YET_RECRUITING

Houston, Texas

ClinicalTrials.gov record


NCT05211570. First posted on 1/27/22

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