CLAG+VEN vs CLAG in the Treatment of Relapsed/Refractory AML

NCT06763666 · Status: NOT_YET_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 172

Last updated 2025-01-08

No results posted yet for this study

Summary

This is a multicenter, prospective, randomized controlled clinical study comparing the efficacy and safety of CLAG+VEN and CLAG regimens in relapsed/refractory(r/r) AML.

Conditions

  • Relapsed/Refractory AML

Interventions

DRUG

Cladribine

Given IV

DRUG

Cytarabine

Given IV

DRUG

G-CSF

Given SC

DRUG

Venetoclax

Given PO

Sponsors & Collaborators

  • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

    collaborator OTHER
  • Guangzhou No.12 People's Hospital

    collaborator OTHER_GOV
  • Guangzhou Panyu Central Hospital

    collaborator OTHER
  • Guangzhou General Hospital of Guangzhou Military Command

    collaborator OTHER
  • Guangzhou First People's Hospital

    collaborator OTHER
  • Foresea Life Insurance Guangzhou General Hospital

    collaborator UNKNOWN
  • Guangdong Second Provincial General Hospital

    collaborator OTHER
  • Jiangmen Central Hospital

    collaborator OTHER
  • Shantou Central Hospital

    collaborator OTHER
  • Maoming People's Hospital

    collaborator OTHER
  • First Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • Hainan General Hospital

    collaborator OTHER
  • Dongguan People's Hospital

    collaborator OTHER_GOV
  • Tungwah Hospital of Sun Yat-Sen University

    collaborator UNKNOWN
  • Shenzhen Hospital of Southern Medical University

    collaborator OTHER
  • Central People's Hospital of Zhanjiang

    collaborator OTHER
  • ZhuHai Hospital

    collaborator OTHER
  • Shenzhen Second People's Hospital

    collaborator OTHER
  • Zhongshan People's Hospital, Guangdong, China

    collaborator OTHER
  • LiuZhou People's Hospital

    collaborator OTHER
  • First People's Hospital of Foshan

    collaborator OTHER
  • Southern Medical University, China

    collaborator OTHER
  • Affiliated Hospital of Guangdong Medical University

    collaborator OTHER
  • Guilin Medical University, China

    collaborator OTHER
  • Yuebei People's Hospital

    collaborator OTHER
  • Huizhou Municipal Central Hospital

    collaborator OTHER
  • Second Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • Peking University Shenzhen Hospital

    collaborator OTHER
  • Nanfang Hospital, Southern Medical University

    lead OTHER

Principal Investigators

  • Guopan Yu · Nanfang Hospital, Southern Medical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-28
Primary Completion
2025-06-30
Completion
2025-12-31

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06763666 on ClinicalTrials.gov