OncoMatch

OncoMatch/Clinical Trials/NCT03629171

Liposome-encapsulated Daunorubicin-Cytarabine and Venetoclax in Treating Participants With Relapsed, Refractory or Untreated Acute Myeloid Leukemia

Is NCT03629171 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Liposome-encapsulated Daunorubicin-Cytarabine and Venetoclax for recurrent acute myeloid leukemia.

Phase 2RecruitingM.D. Anderson Cancer CenterNCT03629171Data as of May 2026

Treatment: Liposome-encapsulated Daunorubicin-Cytarabine · VenetoclaxThis phase II trial studies how well liposome-encapsulated daunorubicin-cytarabine and venetoclax work in treating participants with acute myeloid leukemia that has come back (relapsed), does not respond to treatment (refractory), or has not been treated (untreated). Drugs used in chemotherapy, such as liposome-encapsulated daunorubicin-cytarabine and venetoclax, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.

Check if I qualify

Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Cannot have received: CPX-351 (CPX-351)

Prior treatment with CPX-351

Cannot have received: BCL2 inhibitor (venetoclax)

Exception: Patients with prior treatment with venetoclax will be allowed in patients with relapsed/refractory (R/R) disease including those in the lead-in phase as well as those in cohort A

Prior treatment with venetoclax. Patients with prior treatment with venetoclax will be allowed in patients with relapsed/refractory (R/R) disease including those in the lead-in phase as well as those in cohort A

Lab requirements

Kidney function

Creatinine <= 1.5 x ULN

Liver function

Bilirubin <= 2 mg/dL; AST and/or ALT <= 3 x ULN or < 5 x ULN if related to leukemic involvement

Cardiac function

Known cardiac ejection fraction of >= 45% within the past 3 months

Bilirubin <= 2 mg/dL; AST and/or ALT <= 3 x ULN or < 5 x ULN if related to leukemic involvement; Creatinine <= 1.5 x ULN; Known cardiac ejection fraction of >= 45% within the past 3 months

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • M D Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify