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Autologous Hematopoietic Stem Cell Transplantation for Early Onset Type 1 Diabetes

Safety and Efficacy Study of Autologous Nonmyeloablative Hematopoietic Stem Cell Transplantation for Early Onset Type 1 Diabetes-a Phase II Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00807651
Enrollment
40
Registered
2008-12-12
Start date
2008-02-29
Completion date
2016-12-31
Last updated
2021-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes Mellitus

Keywords

Diabetes Mellitus, Stem cells, Autologous stem cell transplantation, Autoimmune diseases

Brief summary

This is a phase II trial in individuals who have been diagnosed with type 1 diabetes within the previous 6 months. The study is evaluating whether stem cell transplantation is safe when chemotherapy and immunotherapy are used in combination and if it has immune resetting effect that may halt the immune attack to pancreas islets and thus preserve the body's own insulin production.

Detailed description

Type 1 diabetes is an autoimmune disease in which the immune system mistakenly attacks the insulin-producing beta cells in the pancreas. Generally, at the time someone is diagnosed with type 1 diabetes, not all of a person's beta cells have been destroyed. It's important to preserving the remaining precious beta cells so as to stop the diabetes progression. The exact mechanism of action of Autologous Hematopoietic Stem Cell Transplantation(AHST) in autoimmune disorders is not fully understood. Preliminary data supported post-AHST immune resetting included an increase in thymus-derived naive T cells, decreased central-memory T cells, increased output of recent thymic emigrants, and recovery of a diverse but distinct T-cell receptor repertoire following AHST. In the patients of type 1 diabetes, decreasing titer of anti-GAD antibody may bring improvement of beta-cell function after intensive immunosuppression. Furthermore, there may exit the possibility of regeneration of beta cells from surviving beta cells or from pancreatic or bone marrow stem cells. Patients recently diagnosed (less than 6 months) with type 1 diabetes mellitus proved by positive antibody against glutamic acid decarboxylase will be included in this study. Hematopoietic stem cells will be mobilized with cyclophosphamide (2.0 g/m2) and granulocyte colonystimulating factor (10 μg/kg per day) and then collected from peripheral blood by leukapheresis and cryopreserved. The cells were injected intravenously after conditioning with cyclophosphamide (200 mg/kg) and rabbit antithymocyte globulin (4.5 mg/kg). This procedure is performed in isolated rooms at the Bone Marrow Transplantation Unit of Shanghai Ruijin Hospital affiliated to Shanghai Jiao-Tong University School of Medicine. Patients will be discharged from the hospital 1 month after transplantation and continue the follow-ups for 3 years. Patients fitting the inclusion criteria but not agreeing to perform the transplantation are the control group and they will be followed in parallel with transplanted patients.

Interventions

PROCEDUREAHSCT

All study participants given written informed consent will perform autologous hematopoietic stem cell transplantation(AHSCT) and be treated with immunosuppression.

All study participants not accepted written informed consent will received insulin therapy with consistent or multiply subcutaneous injection.

Sponsors

Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Type 1 diabetes mellitus diagnosed by clinical/metabolic parameters and positive anti-GAD antibody * Less than 6 months from diagnosis

Exclusion criteria

* Previous diabetic ketoacidosis * Pregnancy * Severe psychiatric disorder * Severe organic impairment (renal, hepatic, cardiac, pulmonary) * Active infectious disease * Previous or present neoplastic disease

Design outcomes

Primary

MeasureTime frame
Exogenous insulin dose1 month, 3 months, 6 months, 12 months, 24 months, 36 months

Secondary

MeasureTime frame
Anti-GAD titres1 month, 3 months, 6 months, 12 months, 24 months, 36 months
C-peptide level1 month, 3 months, 6 months, 12 months, 24 months, 36 months
HbA1c level3 months, 6 months, 12 months, 24 months, 36 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026