Autologous Transplantation of Expanded Pancreatic Islet Cells (YD01-2022) in Patients

Shanghai Jiao Tong University School of Medicine (Other)
Overall Status
Recruiting ID

Study Details

Study Description

Brief Summary

This study will evaluate the efficacy and safety of autologous transplantation of expanded pancreatic islet cells in patients with diabetes mellitus after total pancreatectomy.

Condition or Disease Intervention/Treatment Phase
  • Biological: YD01-2022
Phase 2

Study Design

Study Type:
Anticipated Enrollment :
3 participants
Intervention Model:
Single Group Assignment
None (Open Label)
Primary Purpose:
Official Title:
Evaluation of the Efficacy and Safety of Autologous Transplantation of Expanded Pancreatic Islet Cells (YD01-2022) in Patients With Diabetes Mellitus After Total Pancreatectomy
Actual Study Start Date :
Feb 22, 2023
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: YD01-2022

Biological: YD01-2022
Human islet cells were isolated and expanded in vitro to generate islets containing all types of pancreatic endocrine cells and possessing comparable function of human islets. These islet cells will be infused into the hepatic portal vein.

Outcome Measures

Primary Outcome Measures

  1. C-peptide change [12 months post-transplant]

    Evaluation of the magnitude of C-peptide change after transplantation

Secondary Outcome Measures

  1. the proportion of subjects with HbA1c ≤7.0% and no severe hypoglycemic events [52 weeks post-transplant]

  2. The proportion of subjects who are insulin-independent [12 weeks and 52 weeks post-transplant]

  3. The percentage reduction in insulin requirement [12 weeks and 52 weeks post-transplant]

  4. Glycemic control (MAGE) [12 weeks and 52 weeks post-transplant]

    Evaluation of the average amplitude of glycemic fluctuations (MAGE) in subjects

  5. Evaluation of the severity of hypoglycemia using the Ryan Hypoglycemia Severity Score (HYPO) [baseline and 52 weeks post-transplant]

  6. Quality of life score [baseline and 52 weeks post-transplant]

    Evaluation of the quality of life score in subjects

Eligibility Criteria


Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Inclusion Criteria:
  1. Voluntarily sign an informed consent form and comply with the trial treatment plan and visit schedule.

  2. Age ≥18 years and ≤60 years on the day of signing the informed consent form, regardless of gender.

  3. Diagnosed with chronic pancreatitis and indication for total pancreatectomy. 4. Post-total pancreatectomy, experiencing elevated blood glucose levels and meeting the diagnostic criteria for diabetes (World Health Organization, 2019 edition).

  4. Post-mixed meal stimulation, C-peptide level <0.3 ng/mL at 120 minutes. 6. Sexually active males who are not surgically sterilized or have partners of childbearing potential agree to use effective contraception during the entire trial period and for at least 6 months after the study ends; sexually active females of childbearing potential agree to use effective contraception during the entire study period and for at least 6 months after the study ends.

  5. History of diabetes or preoperative diagnosis of hyperglycemia, meeting the diagnostic criteria for diabetes.

  6. Previous pancreatic or islet transplantation.

  7. Uncontrolled hypertension, such as systolic blood pressure (SBP) >160 mmHg and/or diastolic blood pressure (DBP) >100 mmHg despite stable dose (at least 4 weeks) of antihypertensive medication.

  8. Known hemoglobin-related diseases, anemia (moderate to severe), or other known hemoglobinopathies that interfere with HbA1c measurement (such as sickle cell disease).

  9. Impaired liver or kidney function at screening (reference range from the study center's laboratory): aspartate aminotransferase (AST) >3 times the upper limit of normal (ULN), alanine aminotransferase (ALT) >3 times ULN, total bilirubin level (TBL)

2 times ULN (excluding Gilbert's syndrome). Creatinine clearance rate <45 mL/min (calculated by the Cockcroft-Gault formula).

  1. Significant albuminuria (urinary albumin excretion rate >300 mg/g) or history thereof.

  2. Uncontrolled thyroid disease or adrenal insufficiency.

  3. Positive hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) with peripheral blood hepatitis B virus (HBV) DNA ≥104 copies or ≥2000 IU/mL (HBsAg positive with HBV DNA <2000 IU/mL (<104/mL) must receive antiviral treatment throughout the study; HBcAb positive with HBV DNA <2000 IU/mL (<104/mL) require regular monitoring of HBV DNA quantification throughout the study); Hepatitis C virus (HCV) antibody positive with peripheral blood HCV RNA ≥103 IU/mL; Human immunodeficiency virus (HIV) antibody positive; Active syphilis infection (cured cases may be included); Cytomegalovirus (CMV) DNA positive; Positive nucleic acid test for novel coronavirus (COVID-19).

  4. Severe heart disease or a history of cardiovascular disease within 6 months before screening, including stroke, decompensated heart failure (NYHA class III or IV), myocardial infarction, unstable angina, or coronary artery bypass grafting.

  5. Previous history of coagulation disorders or requiring long-term anticoagulant therapy (e.g., warfarin) (low-dose aspirin therapy is allowed) or patients with INR >1.5.

  6. Substance abusers with a history of drug abuse/dependence or drug use within 1 year before screening.

  7. Received live virus vaccines within the past 6 months or planned to receive live virus vaccines during the trial or within 1 month after treatment. Live vaccines include, but are not limited to, measles, mumps, rubella, varicella, yellow fever, rabies, Bacillus Calmette-Guérin, typhoid vaccine, COVID-19 vaccine, etc.

  8. Previous history of pancreatic cancer, intraductal papillary mucinous neoplasm of the pancreas, end-stage lung disease, or liver cirrhosis.

  9. Other abnormal laboratory test results deemed clinically significant by the investigator.

  10. Patients with severe mental illness.

  11. Participated in a drug or medical device clinical trial within the past 3 months and received investigational drugs or medical devices; or within 5 half-lives of another drug before screening (if the half-life exceeds 3 months).

  12. Currently receiving long-term (continuous for ≥14 days) systemic pharmacological doses of glucocorticoids or other medications that may affect the participant's consciousness.

  13. Treatment (local, intra-articular, intraocular, or inhalation preparations) for any other factors or diseases not mentioned above, deemed unsuitable for participation in this clinical study by the investigator.

Contacts and Locations


Site City State Country Postal Code
1 Department of Endocrinology and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao-Tong University Shanghai China 200025

Sponsors and Collaborators

  • Shanghai Jiao Tong University School of Medicine


None specified.

Study Documents (Full-Text)

None provided.

More Information


None provided.
Responsible Party:
Shanghai Jiao Tong University School of Medicine Identifier:
Other Study ID Numbers:
  • YD01-2022
First Posted:
Aug 14, 2023
Last Update Posted:
Aug 14, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD:
Studies a U.S. FDA-regulated Drug Product:
Studies a U.S. FDA-regulated Device Product:

Study Results

No Results Posted as of Aug 14, 2023