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NCT06050941

Reduced Intensive Idarubicin and Cytarabine Plus Venetoclax as First-line Treatment for Adults AML and MDS

Not yet recruiting Phase 2 Last updated 5 March 2024
What this trial tests

Phase 2 trial testing idarubicin in Acute Myeloid Leukemia in 60 participants. Not yet recruiting.

Timeline
2 April 2024
Primary endpoint
2 April 2026
2 April 2027

Quick facts

Lead sponsorFirst Affiliated Hospital of Zhejiang University
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment60
Start date2 April 2024
Primary completion2 April 2026
Estimated completion2 April 2027

Drugs / interventions tested

Conditions studied

Sponsor

First Affiliated Hospital of Zhejiang University

Who can join

Adults 18 to 60, any sex, with Acute Myeloid Leukemia or Myelodysplastic Syndromes. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Reduced intensive 3 + 5 idarubicin and cytarabine chemotherapy plus venetoclax as first-line treatment for adults with acute myeloid leukaemia and high-risk myelodysplastic syndrome

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Advances in the Treatment of Acute Myeloid Leukemia: Implications for Low- and Middle-Income Countries.
    Morcos-Sandino M, Quezada-Ramírez SI, Gómez-De León A. · · 2025 · cited 1× · PMID 40427048 · DOI 10.3390/biomedicines13051221

Verify or expand the search:

Other trials of idarubicin

Trials testing the same drug.

Other recruiting trials for Acute Myeloid Leukemia

Currently open trials in the same condition.

Other First Affiliated Hospital of Zhejiang University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06050941.

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