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NCT01909245Active, not recruitingPhase 2

Islet Cell Transplant for Type 1 Diabetes

Islet Transplantation Using a T-Cell Depleting Immunosuppression Induction Regimen

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

City of Hope National Medical Center, located in Duarte, CA, is hosting a clinical study on islet cell transplantation, an experimental procedure being evaluated as a treatment for patients with type 1 diabetes. Islet cell transplantation involves taking insulin-producing cells from organ donors and transplanting them into the liver of a patient with diabetes. Once transplanted, the islets produce insulin, which can improve blood sugar control and eliminate the need to inject insulin or use an insulin pump. Anti-thymocyte globulin (ATG) and alemtuzumab (Campath) are anti-rejection medications that work by decreasing a patient's T-cells. T-cells are special white blood cells that recognize and destroy unwanted things like infections but can also attack transplanted cells and organs. Reducing the number of T-cells at the time of transplant may protect islets and improve long-term transplant success. In previous research studies, islet transplantation has been successful in reducing low blood sugar episodes, improving overall blood sugar control, and in some cases, allowing patients with type 1 diabetes to stop taking insulin. The purpose of this study is to determine if islet cell transplantation using ATG or alemtuzumab, along with additional medications to prevent the body from rejecting the transplanted cells, is a safe and effective treatment for type 1 diabetes. Study participants may receive up to three islet transplants and will be followed for five years to monitor blood sugar control, islet transplant function, and changes in quality of life.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
10 (actual)
First submitted
22 Jul 2013
Start date
10 Jul 2015
Primary completion date
31 Aug 2027
Lead sponsor
City of Hope Medical Center
NCT number
NCT01909245

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 10
  • From 10 Jul 2015 to the primary completion date, 31 Aug 2027
  • 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

  • Increased risk of bleeding, other chronic hemostasis disorders, or treatment with chronic anticoagulant therapy
  • Previous organ/tissue transplant, except as noted above
  • Administration of live attenuated vaccines within 2 months of enrollment
  • Presence of a chronic disease that must be chronically treated with a contraindicated agent
  • 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 prior to study entry and for as long as they are on immunosuppression medication, and women presently breast feeding are excluded

Other illness

  • Significant liver/gall bladder disease
  • Significant cardiovascular disease
  • Anemia or other blood disorders that require medical treatment
  • Recent unresolved acute infection (except for mild skin infection or nail fungal infection), or chronic infection
  • Any history of malignancy, except for completely resected squamous or basal cell carcinoma of the skin or in situ cancer of the cervix
  • Recent history of non-adherence to medical treatment, or inability to demonstrate capacity to comply with strict blood glycemic control and insulin therapy
  • Psychiatric illness that is untreated, or likely to interfere significantly with study compliance despite treatment
  • History of gastric bypass
  • Any medical condition that in the opinion of the investigator will interfere with safe participation in the trial

Lab values

  • WBC \<3,000/ul

Other

  • Body Mass Index (BMI) \> 33
  • Insulin requirements \> 1.2 units/kg/day
  • Known sensitization to both rATG -and- alemtuzumab
  • Significant kidney dysfunction
  • Active proliferative retinopathy
  • High blood pressure despite appropriate treatment
  • High cholesterol/triglycerides despite appropriate treatment
  • Epstein-Barr Virus (EBV) IgG negative
  • Active alcohol or substance abuse, including cigarette smoking
  • Individuals without health insurance

Who the study is looking for

  • Age 18-68 years
  • Type 1 diabetes mellitus for at least 5 years
  • Ability and willingness to comply with post-transplant regimen, including taking anti-rejection medications, use of reliable contraception, frequent clinic visits, lab tests, careful recording of blood glucose values, insulin doses and medications, and completing detailed follow-up studies
    • Additional Inclusion Criteria nITA Candidates Only
  • Unstable blood sugar control characterized by:
    • Frequent hypoglycemia (blood glucose ≤ 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
    • Additional Inclusion Criteria for RT Candidates Only
  • One or two or previous islet transplants \> 1 month prior to screening with continuing insulin requirements and/or HbA1c \> 6.5%
    • Additional Inclusion Criteria for IAK Candidates Only
  • Successful kidney transplant \> 3 months prior to screening
  • Stable maintenance immunosuppression consisting of tacrolimus alone or in conjunction with sirolimus, mycophenolate mofetil, myfortic or azathoprine; or cyclosporine in conjunction with sirolimus, mycophenolate mofetil, or myfortic +/- ≤ 10 mg/day corticosteroids
  • No history of acute rejection related to kidney graft in last 12 months and low risk of rejection
  • Under continuing care of physician for kidney graft, who has provided letter in support of candidate's consideration for study participation

Criteria the registry did not label

  • Three different categories of patients with Type 1 Diabetes will be considered for study participation:
  • Naïve islet transplant alone (nITA) candidates: T1D patients complicated by frequent/severe hypoglycemia, hypoglycemia unawareness, AND/OR otherwise unstable blood glucose control who have not received a previous transplant (except for a failed pancreas more than 6 months prior to screening)
  • Repeat transplant (RT) candidates: T1D patients who have received two or fewer previous islet transplants \> 1 month prior to screening, but continue to require exogenous insulin treatment or have an HbA1c \> 6.5%
  • Islet after kidney transplant (IAK) candidates: T1D patients with a history of successful renal transplant \> 3 months prior to screening

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 StatesUnknown status

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