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NCT06810791

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

Recruiting now Phase 3 Last updated 6 February 2025
What this trial tests

Phase 3 trial testing HVA in Newly Diagnosed Acute Myeloid Leukemia With High Risk in 876 participants. Currently enrolling.

Timeline
1 January 2025
Primary endpoint
30 June 2026
31 December 2026

Quick facts

Lead sponsorNanfang Hospital, Southern Medical University
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment876
Start date1 January 2025
Primary completion30 June 2026
Estimated completion31 December 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Nanfang Hospital, Southern Medical University

Who can join

18 and older, any sex, with Newly Diagnosed Acute Myeloid Leukemia With High Risk. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of HVA

Trials testing the same drug.

Other Nanfang Hospital, Southern Medical 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/NCT06810791.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing