Skip to main content
OpenTrials
Completed

NCT Number: NCT05308836

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

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)

Completed

Looking for future studies?

Notify Me

Key information

Age range

5 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Vinmec Research Institute of Stem Cell and Gene Technology

Hanoi, 10000, Vietnam

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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.
  • The time from the diagnosis of type 1 diabetes to enrollment ≤ 12 months.
  • Blood testing conducted at the time of diagnosis:
  • Fasting blood glucose ≥ 7 mmol / L,
  • HbA1C ≥ 6.5%.
  • Have at least one antibodies associated with T1D such as ICA; GAD; ZnT8 or IAA.
  • At the time of screening at Vinmec for study enrollment, patients are actively managing their blood glucose levels with insulin.
  • 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

Treatment and study plan

adipose-derived messenchymal stem cell

Combination Product

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

Primary outcomes

  1. Safety measure

    Time frame: 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 outcomes

  1. HbA1c

    Time frame: 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)

    Time frame: 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

    Time frame: up to the 6-month period following treatment

    C-peptide levels

  4. Blood insulin

    Time frame: up to the 6-month period following treatment

    Blood insulin

  5. Insulin dose

    Time frame: up to the 6-month period following treatment

    Insulin dose

Sponsors and collaborators

Lead sponsor

Vinmec Research Institute of Stem Cell and Gene Technology

Other

Collaborators

  • Gwoxi Stem cell applied technology Company

Registry information

Official study title

Phase I Open Label Clinical Trial to Evaluate Safety of Adipose Derived Mesenchymal Stem Cell Transplantation for Type 1 Diabetes Treatment

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Apr 4, 2022
Registry last updated
Aug 17, 2025

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.

Published trials that share one or more normalized conditions with this study.