HVA vs IA/DA or VA in the Treatment of ND HR-AML

Recruiting Phase 3 Interventional Study
Newly Diagnosed Acute Myeloid Leukemia With High Risk
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
876 (estimated)
Sponsor
Nanfang Hospital, Southern Medical University · Other
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About This Trial

The aim of this study is to evaluate the safety and efficacy of homohartonine combined with venetoclax and azacitidine (HVA) versus intensive chemotherapy (IA/DA) or venetoclax combined with azacitidine (VA) in newly diagnosed high-risk AML patients.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * According to the world health organization (WHO) classification of newly diagnosed with AML patients; * Age ≥18 years old; * High-risk patients should meet any of the following criteria: ① High risk group according to the European Leukemia Risk stratification (ELN) 2022; (2) S…
Contacts

Guopan Yu

+8615876559968

yugpp@163.com

CONTACT