Evaluate Safety of Adipose Derived Mesenchymal Stem Cell Transplantation for Type 1 Diabetes Treatment

Sponsor
Vinmec Research Institute of Stem Cell and Gene Technology (Other)
Overall Status
Recruiting
CT.gov ID
NCT05308836
Collaborator
Gwoxi Stem cell applied technology Company (Other)
10
1
1
24.8
0.4

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the safety of intravenously (IV) administered adipose-derived mesenchymal stem cell (AD-MSC) in patients with type 1 diabetes mellitus (T1D)

Condition or Disease Intervention/Treatment Phase
  • Combination Product: adipose-derived messenchymal stem cell
Phase 1

Detailed Description

Adipose derived mesenchymal stem cells (AD-MSCs) has many advantages, i.e. the greater ease of access and harvesting by means such as subcutaneous lipoaspiration, a much less painful procedure than harvesting bone marrow stem cells, and a much less ethical concern because they are harvested from autologous fat. The purpose of this study is to evaluate the safety of intravenously (IV) administered adipose-derived mesenchymal stem cell (AD-MSC) in treatment 10 patients with type 1 diabetes mellitus (T1D) at Vinmec International Hospital, Hanoi, Vietnam.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Phase I Open Label Clinical Trial to Evaluate Safety of Adipose Derived Mesenchymal Stem Cell Transplantation for Type 1 Diabetes Treatment
Actual Study Start Date :
Oct 4, 2021
Anticipated Primary Completion Date :
Oct 30, 2022
Anticipated Study Completion Date :
Oct 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Adipose-derived messenchymal stem cell (AD-MSC)

Intervention: Intravenousling (IV) AD-MSC in 10 patients with type 1 diabetes mellitus.

Combination Product: adipose-derived messenchymal stem cell
Collaborative research program between Vinmec Research Institute of Stem Cell and Gene Technology with the National Yang-Ming University in Taiwan The adipose mesenchymal stem cell line (GXIPC1) was collected from healthy donors who have screened for infectious diseases and then multiplied in large numbers. These products were produced following the GMP laboratory system and approved by Taiwan FDA for preclinical and clinical trials with completed certificates

Outcome Measures

Primary Outcome Measures

  1. Safety measure [up to the 6-month period following treatment]

    Safety is recognized as number of adverse events (AE) and serious adverse events (SAE) appear from the time that patients sign in ICF

Secondary Outcome Measures

  1. HbA1c [up to the 6-month period following treatment]

    A hemoglobin A1c (HbA1c) test measures the amount of blood sugar (glucose) attached to hemoglobin

  2. Fasting blood glucose (FPG) [up to the 6-month period following treatment]

    Fasting blood glucose (FPG) measures the levels of glucose (sugar) in the blood

  3. C-peptide levels [up to the 6-month period following treatment]

    C-peptide levels

  4. Blood insulin [up to the 6-month period following treatment]

    Blood insulin

  5. Insulin dose [up to the 6-month period following treatment]

    Insulin dose

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient diagnosed T1D (according to the instructions of the Ministry of Health No: 5481/QD-BYT dated December 30, 2020)

  • Aged from 5 years and over.

  • Be within 12 months of diagnosis with T1D

  • Blood test:

  • Fasting blood glucose > 7 mmol / L,

  • 7,5% < HbA1C <10%.

  • Have at least one antibodies associated with T1D such as ICA or GAD

  • The patient does not have other serious acute illness requiring treatment

  • The patient agrees to use stem cell transplant for treatment

  • The patient's parent (parent or legal guardian) can read, write, understand the ICF form and agree to sign a consent to participate in the study.

Exclusion Criteria:
  • Having evidence related to renal dysfunction: creatinine > 1.5 mg/dl or (>133 mmol/L) for boys, creatinine > 1.4 mg/dl or (>124 mmol/L) for girls

  • In case of kidney failure. Proteinuria within the range of nephrotic syndrome (>3.5 g/day or ratio of protein/creatinine in urine >2.7)

  • In case of kidney failure

  • Having severe infection or infected with hepatitis B virus, hepatitis C virus, HIV virus, or tuberculosis

  • Cardiovascular disease, respiratory disease (pulmonary, fibrosis, chronic respiratory failure), liver disease, cancer or neurological disease

  • Blood clotting disorders (INR> 1,5, PTT> 40, PT> 15).

  • Taking any anticoagulant

  • Taking systemic steroids

  • Participate in another clinical study involving experimenting drugs and/or medical equipment

  • History of allergic reaction to anesthetic agents and/or antibiotics

Contacts and Locations

Locations

Site City State Country Postal Code
1 Vinmec Research Institute of Stem Cell and Gene Technology Hanoi Vietnam 10000

Sponsors and Collaborators

  • Vinmec Research Institute of Stem Cell and Gene Technology
  • Gwoxi Stem cell applied technology Company

Investigators

  • Principal Investigator: Liem T Nguyen, Prof, Vinmec Research Institute of Stem Cell and Gene Technology

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Vinmec Research Institute of Stem Cell and Gene Technology
ClinicalTrials.gov Identifier:
NCT05308836
Other Study ID Numbers:
  • ISC20.01
First Posted:
Apr 4, 2022
Last Update Posted:
Apr 4, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Vinmec Research Institute of Stem Cell and Gene Technology
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 4, 2022