STOD3: Repeated Infusions of Mesenchymal Stromal Cells in Children With Osteogenesis Imperfecta

Sponsor
Nationwide Children's Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01061099
Collaborator
(none)
5
1
2
48
0.1

Study Details

Study Description

Brief Summary

This is a study to evaluate the safety and effectiveness of repeated Mesenchymal Stromal Cells (MSC) infusions to patients with Type II or III osteogenesis imperfecta (OI).

Participants will receive MSC infusions approximately every 4 months to complete a total of 6 infusions over 20 months. Participants will be followed for 4 months post their last MSC infusion.

Condition or Disease Intervention/Treatment Phase
  • Biological: Mesenchymal Stromal Cells
Phase 1

Detailed Description

This is a pilot study to evaluate the safety and efficacy of repeated MSC infusions to subjects with OI. This study will evaluate subjects on two separate strata. Stratum A will include subjects with a diagnosis of Type II or Type III osteogenesis imperfecta who have previously undergone a bone marrow transplant. Stratum A may use previously harvested and cryopreserved bone marrow mononuclear cells from original BMT donor or freshly harvested or cryopreserved bone marrow mononuclear cells obtained from a haploidentical healthy parent or sibling. Stratum B will include subjects with Type II or III osteogenesis imperfecta who have not undergone a bone marrow transplant. Stratum B will only receive freshly harvested or cryopreserved bone marrow mononuclear cells from a haploidentical healthy parent or sibling.

Participants will receive MSC infusions approximately every 4 months to complete a total of 6 infusions over 20 months. Participants will be followed for 12 months post their last MSC infusion.

Study Design

Study Type:
Interventional
Actual Enrollment :
5 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Pilot Study to Assess the Safety and Feasibility of Repeated Infusions of Mesenchymal Stromal Cells (MSC) in Children With Osteogenesis Imperfecta
Study Start Date :
Feb 1, 2010
Actual Primary Completion Date :
Mar 1, 2013
Actual Study Completion Date :
Feb 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Stratum A

Subjects with a diagnosis of Type II or Type III osteogenesis imperfecta who have previously undergone a bone marrow transplant. Intervention: Mesenchymal Stromal Cells.

Biological: Mesenchymal Stromal Cells
Both cohorts will receive multiple infusions of ex-vivo expanded MSCs. Stratum A may use previously harvested and cryopreserved bone marrow mononuclear cells from original BMT donor or freshly harvested or cryopreserved bone marrow mononuclear cells obtained from a haploidentical healthy parent or sibling. Stratum B will only receive freshly harvested or cryopreserved bone marrow
Other Names:
  • ex-vivo expanded MSCs
  • Active Comparator: Stratum B

    Subjects with Type II or III osteogenesis imperfecta who have not undergone a bone marrow transplant. Intervention: Mesenchymal Stromal Cells.

    Biological: Mesenchymal Stromal Cells
    Both cohorts will receive multiple infusions of ex-vivo expanded MSCs. Stratum A may use previously harvested and cryopreserved bone marrow mononuclear cells from original BMT donor or freshly harvested or cryopreserved bone marrow mononuclear cells obtained from a haploidentical healthy parent or sibling. Stratum B will only receive freshly harvested or cryopreserved bone marrow
    Other Names:
  • ex-vivo expanded MSCs
  • Outcome Measures

    Primary Outcome Measures

    1. To determine the safety or repeated infusions of donor-derived and MSCs in subjects with severe osteogenesis imperfecta > 5years after an allogeneic bone marrow transplant and no prior bone marrow transplant. [Completion of study]

    Secondary Outcome Measures

    1. To determine if MSCs elicit an immune response after repeated infusions. [Completion of study]

    2. To determine the change in clinical course (growth, bone mineral content, fracture rate, development/activities) of subjects after experimental MSC intervention therapy as compared with each subject's own pre-MSC intervention therapy. [Completion of Study]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 19 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Subjects less than or equal to 19 years of age at the time of enrollment

    • Children with a diagnosis of severe of Type II or III osteogenesis imperfecta

    • Parent or sibling greater than or equal to 18 years of age, donor willing to or has already undergone HLA typing, and willing and able to provide bone marrow

    • BMT greater than 5 years ago for Stratum A

    Exclusion Criteria:
    • Dependent on supplemental oxygen

    • Concurrent Infection

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Children's Hospital of Philadelphia Philadelphia Pennsylvania United States 19104

    Sponsors and Collaborators

    • Nationwide Children's Hospital

    Investigators

    • Principal Investigator: Alix Seif, MD, Children's Hospital of Philadelphia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Edwin Horwitz, Attending Physician, Nationwide Children's Hospital
    ClinicalTrials.gov Identifier:
    NCT01061099
    Other Study ID Numbers:
    • 2008-4-5947
    First Posted:
    Feb 2, 2010
    Last Update Posted:
    Apr 24, 2015
    Last Verified:
    Apr 1, 2015
    Keywords provided by Edwin Horwitz, Attending Physician, Nationwide Children's Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 24, 2015