MSCs Combined With CD25 Monoclonal Antibody and Calcineurin Inhibitors for Treatment of Steroid-resistant aGVHD

NCT02241018 · Status: UNKNOWN · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2014-09-16

No results posted yet for this study

Summary

The purpose of this study is to compare the efficacy of CD25 monoclonal antibody and calcineurin inhibitors with or without mesenchymal stem cells (MSCs) in treating patients with steroid-resistant acute graft-versus-host disease (aGVHD) after allogeneic hematopoietic stem cell transplantation.

Conditions

  • Acute Graft-versus-host Disease

Interventions

DRUG

CD25 monoclonal antibody

DRUG

calcineurin inhibitors

BIOLOGICAL

MSCs

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
2018-09-30
Completion
2018-12-31

Countries

  • China

Study Locations

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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 NCT02241018 on ClinicalTrials.gov