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Umbilical Cord Blood-derived Mesenchymal Stem Cells for the Treatment of Steroid-refractory Acute or Chronic Graft-versus-host-disease (GVHD-MSC)

Primary Purpose

Graft-Versus-Host Disease, GVHD, Allogeneic Hematopoietic Transplant

Status
Unknown status
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Human umbilical cord blood-derived mesenchymal stem cells
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Graft-Versus-Host Disease focused on measuring Graft-Versus-Host Disease, GVHD, Hematopoietic Stem Cell Transplantation, Stem Cell Transplantation, Allogeneic hematopoietic transplant, Mesenchymal Stem Cells, Unrelated Donors, Cord Blood Stem Cell Transplantation

Eligibility Criteria

1 Day - 30 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Steroid-refractory acute or chronic graft-versus-host-disease
  • Acquisition of consent form
  • 0-30 years of age

Exclusion Criteria:

  • Withdrawal from the study
  • Progression of underlying hematologic diseases
  • Severe adverse effects related to the investigational drug

Sites / Locations

  • Department of Pediatrics, Samsung Medical CenterRecruiting

Outcomes

Primary Outcome Measures

Safety of UCB-MSC in SR-GVHD
Vital sign Physical examination ECOG performance status Mixed Lymphocyte Reaction(MLR) Adverse effects related to infusion

Secondary Outcome Measures

Complete, Partial Response Rate at 28 and 180 Days in participants with SR-GVHD treated with UCB-MSC
Complete Response(CR) rate(%) = (Number of CR/Number of Participants)x100 Partial Response(PR)rate(%) = (Number of PR/Number of Participants)x100

Full Information

First Posted
February 23, 2012
Last Updated
March 14, 2012
Sponsor
Samsung Medical Center
Collaborators
Medipost Co Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT01549665
Brief Title
Umbilical Cord Blood-derived Mesenchymal Stem Cells for the Treatment of Steroid-refractory Acute or Chronic Graft-versus-host-disease
Acronym
GVHD-MSC
Official Title
Umbilical Cord Blood-derived Mesenchymal Stem Cells for the Treatment of Steroid-refractory Acute or Chronic Graft-versus-host-disease
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Unknown status
Study Start Date
January 2012 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center
Collaborators
Medipost Co Ltd.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Graft-versus-host-disease (GVHD) is a major complication following allogeneic hematopoietic stem cell transplantation (allo-HSCT) which may cause acute life-threatening morbidity or chronic disabilities. Although corticosteroid, the primary agent to treat GVHD, may be effective for some patients, outcomes of those who are refractory to corticosteroid are dismal. Secondary agents can be used for steroid-refractory cases; however, their efficacy is variable and usually limited. The quality of life issue of chronic GVHD is especially important for pediatric survivors who have longer life expectancy than adults. Many in-vitro and in-vivo data support immunoregulatory properties of mesenchymal stem cells(MSCs)and possibilities of treating diseases caused by immune dysregulation such as GVHD. Recent data revealed that bone marrow-derived MSCs were very useful to treat steroid-refractory acute GVHD, which led to improved overall survival compared with controls. More recently, a number of reports suggest MSCs may also be useful in treating chronic GVHD as well as acute GVHD. It has been also reported that third party MSCs are also useful as well as those from autologous or HLA-matched donors. The investigator recently demonstrated that MSCs obtained from umbilical cord blood (UCB) have similar immunosuppressive properties as bone marrow-MSCs. UCB-MSCs can be obtained without doing any harm to donors that it may be more appropriate source of MSCs than bone marrow for off-the-shelf use. However, little is known about the safety and efficacy of UCB-MSCs in treating GVHD. Therefore, the investigator designed this study to evaluate the safety and efficacy of UCB-MSCs in treating pediatric patients with steroid-refractory acute or chronic GVHD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft-Versus-Host Disease, GVHD, Allogeneic Hematopoietic Transplant, Disorder Related to Transplantation
Keywords
Graft-Versus-Host Disease, GVHD, Hematopoietic Stem Cell Transplantation, Stem Cell Transplantation, Allogeneic hematopoietic transplant, Mesenchymal Stem Cells, Unrelated Donors, Cord Blood Stem Cell Transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Human umbilical cord blood-derived mesenchymal stem cells
Other Intervention Name(s)
PROMOSTEM®
Intervention Description
1st infusion(1x1,000,000 hMSC/kg)IV, 2nd infusion(2x1,000,000 hMSC/kg)IV and 3rd infusion(3x1,000,000 hMSC/kg)IV if no complete response at 28 days.
Primary Outcome Measure Information:
Title
Safety of UCB-MSC in SR-GVHD
Description
Vital sign Physical examination ECOG performance status Mixed Lymphocyte Reaction(MLR) Adverse effects related to infusion
Time Frame
180 days
Secondary Outcome Measure Information:
Title
Complete, Partial Response Rate at 28 and 180 Days in participants with SR-GVHD treated with UCB-MSC
Description
Complete Response(CR) rate(%) = (Number of CR/Number of Participants)x100 Partial Response(PR)rate(%) = (Number of PR/Number of Participants)x100
Time Frame
180 Days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Steroid-refractory acute or chronic graft-versus-host-disease Acquisition of consent form 0-30 years of age Exclusion Criteria: Withdrawal from the study Progression of underlying hematologic diseases Severe adverse effects related to the investigational drug
Facility Information:
Facility Name
Department of Pediatrics, Samsung Medical Center
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hong Hoe Koo, MD, PhD
Phone
+82-2-3410-3524
Email
hhkoo.koo@samsung.com
First Name & Middle Initial & Last Name & Degree
Keon Hee Yoo, M.D., Ph.D.
Phone
+82-2-3410-3532
Email
hema2170@skku.edu
First Name & Middle Initial & Last Name & Degree
Hong Hoe Koo, MD, PhD

12. IPD Sharing Statement

Learn more about this trial

Umbilical Cord Blood-derived Mesenchymal Stem Cells for the Treatment of Steroid-refractory Acute or Chronic Graft-versus-host-disease

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