Decitabine in Combination With Low-dose Cytarabine in Elderly Patients With Acute Myeloid Leukemia

NCT02985372 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-12-07

No results posted yet for this study

Summary

This prospective multicenter clinical study was designed to assess the efficacy and safety of decitabine in combination with low-dose cytarabine induction treatment for elderly patients with newly diagnosed acute myeloid leukemia (AML).

Conditions

  • Acute Myeloid Leukemia, Adult

Interventions

DRUG

Decitabine

All patients were treated with decitabine of 15 mg/ m2 intravenously over 4h for 5 consecutive days (day 1-5) for priming combined with cytarabine of 10 mg/m2 q12h for 10 days (day 4-13).

DRUG

Cytarabine

Sponsors & Collaborators

  • Binzhou Medical University

    collaborator OTHER
  • Shengli Oilfield Hospital

    collaborator OTHER
  • Heze Municipal Hospital

    collaborator OTHER
  • Jinan Military Genaral Hospital

    collaborator UNKNOWN
  • Jinan Central Hospital

    collaborator OTHER
  • Jining Medical University

    collaborator OTHER
  • Linyi People's Hospital

    collaborator OTHER
  • Qingdao University

    collaborator OTHER
  • Rizhao People's Hospital

    collaborator OTHER
  • Qianfoshan Hospital

    collaborator OTHER
  • Qilu Hospital of Shandong University (Qingdao)

    collaborator OTHER
  • Taian City Central Hospital

    collaborator OTHER
  • Taishan Medical University Affiliated Hospital

    collaborator OTHER
  • Weihai Municipal Hospital

    collaborator OTHER
  • Weifang Medical University

    collaborator OTHER
  • Zibo First Hospital

    collaborator OTHER
  • Central Hospital of Zibo

    collaborator OTHER
  • Chunyan Ji

    lead OTHER

Principal Investigators

  • Chunyan Ji, Doctor · Shandong University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2016-12-31
Primary Completion
2018-12-31
Completion
2019-12-31

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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 NCT02985372 on ClinicalTrials.gov