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Completed

NCT Number: NCT00823316

Safety and Efficacy Study of Umbilical Cord Blood-Drived Mesenchymal Stem Cells to Promote Engraftment of Unrelated Hematopoietic Stem Cell Transplantation

The purpose of this study is to evaluate the safety and efficacy of PROMOSTEM (human umbilical cord blood-derived mesenchymal stem cells) at a dose of 1 and 5x1,000,000 hMSC/kg in subject for the promotion of an engraftment and prevention of graft rejection and Graft-Versus-Host Disease after unrelated hematopoietic stem cell transplantation for children with acute leukemia.

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Key information

Conditions

Age range

2 year–19 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Samsung Medical Center

Seoul, 135-710, South Korea

About this study

  • Hematopoietic stem cell transplantation (HSCT) is a procedure in which progenitor cells capable of reconstituting normal bone marrow function are administered to a patient. This procedure has been used to treat adults and children with life-threatening hematological malignancies and congenital immunodeficiency disorders.
  • In HSCT, therapeutic goal is an elimination of disease and enrichment of regenerating capacity to achieve engraftments resulting in continued generation of functional blood elements from the engrafted living cells. Transplantation of unrelated hematopoietic stem cells originating either from adult bone marrow or from peripheral blood often leads to graft-versus host-disease (GvHD), opportunistic infections and graft failure after transplantation.
  • In HSCT, MSC have been used as a therapy for GvHD and other complications. The aim of MSC infusions in HSCT is to use the cells' immunomodulatory effects to promote engraftment and to reduce the immunological reactions giving rise to GvHD.
  • There is a growing interest in co-transplantation of MSC and HSC to improve the donor outcome in the unrelated HSCT condition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient age 2~19 years old with plan to have unrelated hematopoietic stem cell transplantation with acute leukemia
  • Patient never has an experience of hematopoietic stem cell transplantation
  • Patient must have an acute leukemia with a complete remission.
  • Patients must have an ECOG 0~2.
  • No moderate or sever organ dysfunction : Ejection fraction > 45%; Creatinine <2.0 mg/ml; Serum bilirubin < 2 mg/ml; AST/ALT < 200 IU/L.
  • Patient must not have an transplantation with different source of hematopoietic stem cell such as bone marrow and cord blood.
  • Patient must not have an infection needed an administration of non-oral antibiotics.
  • No active severe infection derived form virus or fungus.
  • Each patient / patient's guardian must sign written informed consent.

Exclusion criteria

  • Patient has previously received hematopoietic stem cell transplantation.
  • Patient plans to have a related hematopoietic stem cell transplantation.
  • Patient has a severe internal disease.
  • Patient has enrolled another clinical trial study within last 4 weeks.

Treatment and study plan

Human umbilical cord blood-derived mesenchymal stem cells

Biological

1x1,000,000 hMSC/kg, IV after unrelated HSCT

Other names: PROMOSTEM

Primary outcomes

  1. - Day of neutrophil engraftment - Day of platelet engraftment - Evaluation of chimerism - Evaluation of engraftment rate

    Time frame: 28 and 100 days

Secondary outcomes

  1. - AGVHD grade

    Time frame: 100 days

Sponsors and collaborators

Lead sponsor

Medipost Co Ltd.

Industry

Registry information

Official study title

Phase 1/2 Study of Umbilical Cord Blood-Drived Mesenchymal Stem Cells Infusion for Promotion of Engraftment and Prevention of an Graft Rejection and Graft-versus-Host Disease After Unrelated Hematopoietic Stem Cell Transplantation.

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Jan 15, 2009
Registry last updated
Apr 23, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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