Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06990321

Effectiveness of Medium-Dose Cytarabine Combined With Venetoclax for Consolidation Therapy in Elderly Patients With Intermediate to High-Risk Acute Myeloid Leukemia

A Single-center, Single-arm, Prospective Clinical Study of Intermediate-dose Cytarabine in Combination With Venetoclax for Consolidation Therapy of Middle- and High-risk Acute Myeloid Leukemia in The Elderly

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
68 (estimated)
Sponsor
Yehui Tan · Academic / Other
Sex
All
Age
60 Years – 75 Years
Healthy volunteers
Not accepted

Summary

A Single-center, Single-arm, Prospective Clinical Study of Intermediate-dose Cytarabine in Combination with Venetoclax for Consolidation Therapy of Middle- and High-risk Acute Myeloid Leukemia in the Elderly

Detailed description

This study is designed to be a prospective cohort study conducted at the First Hospital of Jilin University. The target populations of this study are patients with Middle- and High-risk Acute Myeloid Leukemia in the elderly who received intermediate-dose cytarabine in combination with venetoclax for consolidation therapy from June 1, 2025to December 31, 2026. It is expected to enroll 68 subjects in this study. The subjects' data such as demographics and other baseline characteristics, medications, prognosis, will be collected, and statistical analysis of data will be conducted to compare the effectiveness outcome measures

Conditions

Interventions

TypeNameDescription
DRUGIntermediate-dose Cytarabine in Combination with VenetoclaxElderly patients with Middle- and High-risk Acute Myeloid Leukemia who received the Intermediate-dose Cytarabine in Combination with Venetoclax at the First Hospital of Jilin University from March 1, 2024 to December 31, 2026.

Timeline

Start date
2025-06-01
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2025-05-25
Last updated
2025-08-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06990321. Inclusion in this directory is not an endorsement.