Last reviewed · How we verify

NCT06643962

Venetoclax Combined with Intensive Therapy for Acute Myeloid Leukemia Patients with Lower Early Peripheral Blast Clearance Rate After Standard Induction Therapy

Recruiting now NA Last updated 12 November 2024
What this trial tests

NA trial testing Venetoclax in Leukemia in 83 participants. Currently enrolling.

Timeline
31 October 2024
Primary endpoint
31 December 2025
31 October 2027

Quick facts

Lead sponsorAffiliated Hospital of Nantong University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment83
Start date31 October 2024
Primary completion31 December 2025
Estimated completion31 October 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Affiliated Hospital of Nantong University

Who can join

Adults 18 to 70, any sex, with Leukemia or Leukemia, Myeloid. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This single-center prospective cohort study aims to evaluate the efficacy and safety of Intensifying treatment with Venetoclax along with intensive chemotherapy in patients with newly diagnosed acute myeloid leukemia (AML) except acute promyelocytic leukemia (non-APL) and exhibiting lower early peripheral blast clearance rate (EPBCR) after standard Intensive Induction therapy (3+7 regimen).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Venetoclax

Trials testing the same drug.

Other recruiting trials for Leukemia

Currently open trials in the same condition.

Other Affiliated Hospital of Nantong 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/NCT06643962.

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