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NCT06328179

Clinical Study Protocol for the Treatment of ND-AML and RR-AML With KMT2A Gene Abnormalities Using VHEA.

Recruiting now NA Last updated 25 March 2024
What this trial tests

NA trial testing Venetoclax 100 mg d1,200 mg d2,400 mg d3-14; in Acute Myeloid Leukemia in 34 participants. Currently enrolling.

Timeline
24 May 2022
Primary endpoint
30 December 2027
30 December 2027

Quick facts

Lead sponsorHuai'an First People's Hospital
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment34
Start date24 May 2022
Primary completion30 December 2027
Estimated completion30 December 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Huai'an First People's Hospital

Who can join

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

Sponsor's own description

This study is a clinical trial aimed at evaluating the efficacy and safety of the VHEA(Venetoclax with Homoharringtonine,Etoposide,Cytarabine)regimen in the treatment of newly diagnosed and relapsed/refractory acute myeloid leukemia (AML) with MLL gene abnormalities. This study includes the induction and consolidation phases of AML treatment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Acute Myeloid Leukemia

Currently open trials in the same condition.

Other Huai'an First People's Hospital 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/NCT06328179.

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