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Study of DAC Combined With HAAG Regimen in Newly Diagnosed AML Patients Older Than 60

NCT04083911 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2019-09-10

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and efficacy of DAC combined with HAAG regimen in the induction treatment of newly diagnosed AML patients older than 60 years.

Conditions

Interventions

DRUG

Decitabine, Homoharringtonine, Aclarubicin, Cytarabine and G-CSF

Decitabine:20mg/m2/d, d1\~5, intravenous infusion; Homoharringtonine:1mg/d,d3\~9,intravenous infusion; Aclarubicin:10mg/d, d3\~d6, intravenous infusion; Cytarabine:10mg/m2,q12h,d3-9, subcutaneous injection; Granulocyte colony-stimulating factor: 50-300μg/d (when WBC counts are less than 20×10\^9/L ),subcutaneous injection;

Sponsors & Collaborators

  • Second Affiliated Hospital of Soochow University

    collaborator OTHER

  • Changzhou No.2 People's Hospital

    collaborator OTHER

  • The First People's Hospital of Lianyungang

    collaborator OTHER

  • Jingjiang People's Hospital

    collaborator OTHER

  • Zhangjiagang First People's Hospital

    collaborator OTHER

  • The Second People's Hospital of Huai'an

    collaborator OTHER

  • The Third People's Hospital of Kunshan

    collaborator UNKNOWN

  • The First Affiliated Hospital of Soochow University

    lead OTHER

Principal Investigators

  • Xiaowen Tang, Ph.D. · The First Affiliated Hospital of Soochow University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
60 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-04-01
Primary Completion
2021-05-31
Completion
2022-05-31

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

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 NCT04083911 on ClinicalTrials.gov