Clinical Study of UCB Combined With UC-MSCs in the Treatment of Bone Marrow Failure Disorders

NCT05794425 · Status: RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2023-11-29

No results posted yet for this study

Summary

The multicenter collaborative clinical study conducted a systematic clinical observation in the treatment of bone marrow failure diseases via UCB\&UC-MSCs , in order to observe its clinical efficacy and safety.

Conditions

  • Bone Marrow Failure Disorders

Interventions

DRUG

Cyclosporine A

3-5 mg per kilogram per day.

BIOLOGICAL

Umbilical cord blood & Umbilical cord derived mesenchymal stem cells

Intravenous infusion of umbilical cord blood and umbilical cord derived mesenchymal stem cells (5-8×10\^7) at 1 week interval.

Sponsors & Collaborators

  • Shandong Province Third hospital

    collaborator OTHER
  • Dezhou People's Hospital

    collaborator OTHER
  • Children's Hospital Affiliated to Shandong University

    collaborator UNKNOWN
  • The Second Affiliated Hospital of Shandong First Medical University

    collaborator OTHER
  • Tai'an Central Hospital

    collaborator UNKNOWN
  • Linyi People's Hospital

    collaborator OTHER
  • Rizhao People's Hospital

    collaborator OTHER
  • Lanling People's Hospital

    collaborator UNKNOWN
  • Jining First People's Hospital

    collaborator OTHER
  • Jining Medical University

    collaborator OTHER
  • Zibo Municipal Hospital

    collaborator OTHER
  • Binzhou People's Hospital

    collaborator OTHER
  • The Affiliated Hospital of Binzhou Medical College

    collaborator UNKNOWN
  • Shengli Oilfield Hospital

    collaborator OTHER
  • Weihai Municipal Hospital

    collaborator OTHER
  • Weihai Central Hospital

    collaborator OTHER
  • Shandong University of Traditional Chinese Medicine

    collaborator OTHER
  • Gansu Provincial Hospital of Traditional Chinese Medicine (TCM)

    collaborator UNKNOWN
  • Wuwei People's Hospital

    collaborator UNKNOWN
  • Gansu Wuwei Tumor Hospital

    collaborator OTHER
  • The Second Affiliated Hospital of Harbin Medical University

    collaborator OTHER
  • Yuncheng Institute of Hematology

    collaborator UNKNOWN
  • Kaifeng Central Hospital

    collaborator OTHER
  • Zhengzhou Central Hospital

    collaborator OTHER
  • Air Force Hospital of Western War Zone

    collaborator UNKNOWN
  • The First People' s Hospital of Yunnan Province

    collaborator UNKNOWN
  • Zigong No.1 Peoples Hospital

    collaborator OTHER
  • The First People's Hospital of Jingzhou

    collaborator OTHER
  • Jiangxi Province Children's Hospital

    collaborator OTHER
  • Second Affiliated Hospital of Zhengzhou University

    collaborator OTHER
  • Yantai Ludong Hospital (Shandong Provincial Hospital Group)

    collaborator UNKNOWN
  • Shandong Qilu Stem Cells Engineering Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • zhe Yu, MD · Shandong Province Third hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-01
Primary Completion
2025-04-30
Completion
2026-04-30

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 NCT05794425 on ClinicalTrials.gov