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NCT03746769RecruitingPhase 1/2

Improving Islet Transplantation Outcomes With Gastrin for Type I Diabetes

Improving Islet Transplantation Outcomes With Gastrin

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

This clinical study will evaluate the safety and effectiveness of Gastrin treatment with islet transplantation to help patients with difficult to control type 1 diabetes make insulin again and improve blood sugar control. This study involves two investigational (experimental) products not yet approved by the U.S. Food and Drug Administration (FDA) as a treatment for any disease: 1. Human allogenic islet cells (islet cells from a deceased, unrelated human donor) 2. Gastrin-17 (Gastrin) - a hormone secreted by the gut

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
20 (estimated)
First submitted
9 Nov 2018
Start date
29 May 2019
Primary completion date
1 Aug 2028
Lead sponsor
City of Hope Medical Center
NCT number
NCT03746769

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 20
  • From 29 May 2019 to the primary completion date, 1 Aug 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous organ/tissue transplant
  • Administration of live attenuated vaccines within 60 days of enrollment.
  • Presence of a chronic disease that must be chronically treated with contraindicated medications
  • Use of investigational agents within four weeks of enrollment
  • Pregnant women, women intending future pregnancy, women of reproductive potential who are unable or unwilling to follow effective contraceptive measures (i.e., tubal ligation, two barrier methods, abstinence) for the duration of study treatment and for as long as they are on immunosuppressive medication, and women presently breastfeeding.

Other illness

  • Hypertension( \>/= 140/90) despite appropriate treatment
  • Recent unresolved acute infection (except for mild skin infection or nail fungal infection), or chronic infection, including tuberculosis, HIV, HBV, HCV, CMV or syphilis (RPR)
  • Any history of malignancy, except completely resected squamous or basal cell skin cancer or in situ cancer of the cervix
  • Evidence of active peptic ulcer disease
  • History of gastric bypass
  • Recent history of non-adherence to recommended medical therapy
  • Psychiatric illness that is untreated, or likely to interfere significantly with study compliance despite treatment
  • Any medical condition that in the opinion of the investigator will interfere with safe participation in the trial

Lab values

  • Significant kidney disease (estimated GFR from serum creatinine measurement \<65 ml/min, random spot urine microalbumin to creatinine ratio \>300mg albumin/g creatinine)
  • Significant hepatobiliary disease, including elevation of liver enzymes \> twice the upper limit of normal for each of ALT and AST (any elevation of these enzymes will be determined), bilirubin not within normal limits, albumin \< 3.5 g/dl, liver masses, portal vein thrombosis, evidence of portal hypertension, or significant, untreated gallbladder disease (i.e. gallstones)
  • Significant cardiovascular disease, including non-correctable coronary artery disease with ejection fraction \< 50% and/or recent myocardial infarction (within last 12 months); or extensive peripheral vascular disease not correctable by surgery,
  • Hyperlipidemia (total cholesterol \> 260 mg/dl, LDL \> 160 mg/dl, and/or triglycerides \> 300 mg/dl) despite appropriate treatment
  • Anemia (Hgb \< 11 g/dl) or other hematologic disorders that require medical attention
  • WBC \<3,000/ul
  • Increased risk of bleeding (platelet count \< 120,000 cells/ul; INR \> 1.5), other chronic hemostasis disorders, or treatment with chronic anticoagulant therapy (i.e. heparin or warfarin)
  • Individuals without health insurance covering the cost of immunosuppression and clinical and laboratory follow-up after completion of the study

Other

  • BMI \> 33
  • Insulin requirements \> 1.0 units/kg/day
  • Evidence of active proliferative retinopathy
  • EBV IgG negative
  • Active alcohol or substance abuse, including cigarette smoking (must be abstinent for \> 3 months)

Who the study is looking for

  • Age 18-68 years
  • Type 1 diabetes mellitus (documented with fasting C-peptide level of \</= 0.2 ng/ml before and \</= 0.3 ng/ml after IV administration of 1 mg of glucagon) for at least 5 years.
  • Unstable blood glucose characterized by:
    • Frequent hypoglycemia (blood glucose less than or equal to 54 mg/dl more than once per week)
    • -and/or- Hypoglycemia unawareness (Clarke score of 4 or more).
    • -and/or- One or more severe hypoglycemic episodes in 12 months preceding enrollment
    • -and/or- Erratic blood glucose levels that interfere with daily activities
    • -and/or- One or more hospital visits for diabetic ketoacidosis in the 12 months preceding enrollment
  • Ability and willingness to comply with post-transplant regimen, including immunosuppression, use of reliable contraception, frequent clinic visits, testing and maintaining detailed logs of blood glucose levels, insulin doses and medications, and completing detailed follow-up studies.
  • Ability to give informed consent.
  • Fully vaccinated against COVID-19

Age in the registry: 18 years to 68 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
City of Hope Medical Center
Coordinator of this site? Confirm its status
DuarteUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.