Mesenchymal Stem Cells Co-transplantation in Alternative Donor Transplantation of Severe Aplastic Anemia.

NCT02247973 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2014-09-25

No results posted yet for this study

Summary

The study is a phase II trial designed to evaluate the efficacy and safety of co-transplantation with bone marrow derived mesenchymal stem cells from related donors in alternative donor transplantation of severe aplastic anemia.

Conditions

  • Severe Aplastic Anemia

Interventions

BIOLOGICAL

mesenchymal stem cells

Intravenous administration of up to 1\~2x10\^6 MSCs per kg,for 2 times,d0 and d14

BIOLOGICAL

mesenchymal stem cells

bone marrow derived mesenchymal stem cells from related donors.

Sponsors & Collaborators

  • Guangzhou First People's Hospital

    collaborator OTHER
  • Nanfang Hospital, Southern Medical University

    collaborator OTHER
  • Southern Medical University, China

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

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

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

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

    collaborator OTHER
  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • The Second People's Hospital of GuangDong Province

    collaborator OTHER
  • First Affiliated Hospital of Jinan University

    collaborator OTHER
  • The First Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • Second Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • Peking University Shenzhen Hospital

    collaborator OTHER
  • Shenzhen Second People's Hospital

    collaborator OTHER
  • Guangzhou General Hospital of Guangzhou Military Command

    lead OTHER

Principal Investigators

  • Yang Xiao, MD · Guangzhou General Hospital of Guangzhou Military Command

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2017-02-28
Completion
2018-02-28

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 NCT02247973 on ClinicalTrials.gov