Hematopoietic Stem Cell Transplantation in Type 1 Diabetes Mellitus

Sponsor
Dra. Olga Graciela Cantu Rodriguez (Other)
Overall Status
Completed
CT.gov ID
NCT01121029
Collaborator
(none)
15
1
1
31
0.5

Study Details

Study Description

Brief Summary

The purpose of this study is to determine if autologous nonmyeloablative hematopoietic stem cell transplantation is able to induce prolonged and significant increases of C-peptide levels associated with absence of or reduction of daily insulin.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Autologous hematopoietic stem cell transplantation
Phase 1/Phase 2

Detailed Description

Patients with type 1 DM depend on exogenous insulin administration for survival and for control of long-term complications. The best-established treatment is tight control of blood glucose achieved by frequent daily injections or continuous subcutaneous infusion of insulin, ie, intensive insulin therapy. Although insulin therapy has developed enormously, even the most modern technologies do not allow the maintenance of normoglycemia.

Since the establishment of the autoimmune etiology of type 1 DM in the late 1970s, many clinical trials analyzing the effects of different types of immune interventions demonstrated that beta-cell preservation is an achievable target in different degrees.

Controlled trials and further biological studies are necessary to confirm the role of this treatment in changing the natural history of type 1 DM.

This is a prospective pilot study which will enroll patients with type 1 diabetes mellitus within the first months of diagnosis, with clinical and laboratory findings. The donor stimulation will be with cyclophosphamide, filgrastim, and mesna. The cells will be recollected from peripheral blood by apheresis and refrigerated. The patients will receive a nonmyeloablative conditioning regimen with cyclophosphamide and fludarabine, and after this, the cells will be injected intravenously. They will receive a standard regimen of post-transplant prophylaxis. The duration of use of this prophylactic drugs scheme depends on the patient's recovery time. The reinfusion of stem cells will be completed after the last dose of cyclophosphamide, through a peripheral vein.

Lately, every three months, the C-Peptide levels, glucose and insulin serum levels will be measured.

Study Design

Study Type:
Interventional
Actual Enrollment :
15 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Autologous Hematopoietic Stem Cell Transplantation in Type 1 Diabetes Mellitus
Study Start Date :
May 1, 2010
Actual Primary Completion Date :
Dec 1, 2011
Actual Study Completion Date :
Dec 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Hematopoietic stem cells

Procedure: Autologous hematopoietic stem cell transplantation
Patients will receive a stimulation with filgrastim 10mcg/Kg per day during 4 days and cyclophosphamide 1.5g/m2 per day during 2 days and mesna 300mg/m2 i.v. in 4 hours for prophylaxis (uroprotection). Lately, the stem cells will be recollected by apheresis. After that, the patients will receive a conditioning regimen with cyclophosphamide 500mg/m2 per day during 4 days and fludarabine 30mg/m2 per day during 4 days. After the last dose of cyclophosphamide, the autologous hematopoietic stem cell transplantation will be done on day 0, by peripheral vein. Then, a standard regimen of prophylaxis with oral ciprofloxacin 500mg every 12 hours, acyclovir 400mg every 8 hours, fluconazole 100mg per day and omeprazole 20mg per day for the recovery time of each patient.
Other Names:
  • Stem cell therapy
  • Outcome Measures

    Primary Outcome Measures

    1. C-peptide levels before and after the hematopoietic stem cell transplantation [Every 3 months for 1 year.]

    Secondary Outcome Measures

    1. Serum levels of Hb A1C before and after the hematopoietic stem cell transplantation [Every month for 1 year.]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    2 Years to 35 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with newly diagnosed in type 1 diabetes mellitus
    Exclusion Criteria:
    • Patients with HIV

    • Patients with Hepatitis

    • Patients with hematologic disease

    • Patients with hearth failure

    • Renal, Hepatic or psychiatric disease

    • Pregnant patients

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital Universitario Dr. José Eleuterio González Monterrey Nuevo Leon Mexico 64460

    Sponsors and Collaborators

    • Dra. Olga Graciela Cantu Rodriguez

    Investigators

    • Principal Investigator: Fernando J Lavalle, MD, Hospital Universitario Dr. José Eleuterio González
    • Study Chair: David Gómez, MD, Hospital Universitario Dr. José Eleuterio González
    • Study Director: Olga G Cantú, MD, Hospital Universitario Dr. José Eleuterio González

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Dra. Olga Graciela Cantu Rodriguez, Autologous Hematopoietic Stem Cell Transplantation in Type 1 Diabetes Mellitus, Hospital Universitario Dr. Jose E. Gonzalez
    ClinicalTrials.gov Identifier:
    NCT01121029
    Other Study ID Numbers:
    • EN10-011
    First Posted:
    May 12, 2010
    Last Update Posted:
    Dec 10, 2012
    Last Verified:
    Dec 1, 2012
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 10, 2012