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Study identifier: NCT06621212 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Mitoxantrone Hydrochloride Liposome, Standard-dose of Cytarabine and Venetoclax in the Treatment of R/R AML

Condition: Relapsed/Refractory Acute Myeloid Leukaemia · Myeloid Malignancy  ·  Sponsor: First Affiliated Hospital of Zhejiang University

PhasePhase 2
Planned participants72
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this prospective, multi-center, single-arm, phase 2 study is to evaluate the efficacy and safety of a combination regimen of mitoxantrone hydrochloride liposome injection, standard-dose of cytarabine and venetoclax (MAV) in the treatment of relapsed or refractory (R/R) AML. The study plan to enroll 72 R/R AML patients who are expected to receive laboratory tests of bone marrow and blood specimens at regular times after MAV treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Jie Jin, M.D.  ·  +86 571-87236896  ·  jiej0503@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiliated Hospital, Zhejiang University School of MedicineHangzhou, Zhejiang, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06621212