Megakaryocytic Progenitor Cells for Prophylaxis and Treatment of Thrombocytopenia

NCT02241031 · Status: UNKNOWN · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2014-09-16

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy of ex vivo generated megakaryocytic progenitor cells (MPs) in prophylaxis and treatment of thrombocytopenia caused by chemotherapy in patients with acute leukemia (AL).

Conditions

Interventions

BIOLOGICAL

MPs

MPs are generated from cord blood using a combination of cytokines.

DRUG

thrombopoietin (TPO) and interleukin-11

Platelet stimulating factors include thrombopoietin (TPO) and interleukin-11 and so on.

Sponsors & Collaborators

  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • Third Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • Guangzhou General Hospital of Guangzhou Military Command

    collaborator OTHER
  • Guangzhou First People's Hospital

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

    collaborator OTHER
  • Southern Medical University, China

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • Huazhong University of Science and Technology

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • Academy Military Medical Science, China

    collaborator INDUSTRY
  • Nanfang Hospital, Southern Medical University

    lead OTHER

Principal Investigators

  • Qifa Liu, MD · Nanfang Hospital, Southern Medical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2016-09-30
Completion
2016-12-31

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 NCT02241031 on ClinicalTrials.gov