CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 21 enrolled
Drug / intervention
Islets of Langerhans transplantationbiological
Likely dose
Islets of Langerhans transplantation 20 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00679042
NCT00679042Phase 3Active

Islet Transplantation in Type 1 Diabetic Patients Using the UIC Protocol, Phase 3

CellTrans Inc.·interventional·Posted May 16, 2008·Updated Apr 6, 2026

In Brief

A Phase 3 clinical trial evaluating Islets of Langerhans transplantation for Type 1 Diabetes Mellitus. Active but no longer recruiting, targeting 21 participants across 1 site.

Detailed Summary

In an earlier Phase 1/2 clinical trial using the Edmonton Protocol of steroid free immunosuppression, investigators at University of Illinois at Chicago (UIC) demonstrated the safety of islet preparation, iset transplantation, and medical treatment at UIC. Therefore, the primary purpose of the present Phase 3 clinical trial is to demonstrate the safety and efficacy of allogeneic islet transplantation in improving glycemic control in Type 1 diabetic patients using the UIC protocol that was developed and proven effective during the Phase 1/2 clinical trial.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 3ActiveOverdue
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 16, 2008
Enrollment StartSep 5, 2007
Primary CompletionJul 19, 2017
Study CompletionJun 14, 2026
TodayJul 2, 2026
Enrollment to primary: 9.9 yearsPosted 18.1 years ago

Interventions

Islets of Langerhans transplantationbiological

Each subject may receive 1-3 transplantations of allogeneic human islets of Langerhans and the following medications: Basiliximab 20 mg iv 2 hours before transplant and 20 mg iv 2 weeks post-transplant; Tacrolimus 1 mg p.o. bid adjusted to reach target trough levels of 3-6 ng/ml; Sirolimus 0.2 mg/kg loading dose, then 0.1 mg/kg p.o. daily adjusted to reach target trough levels of 10-15 ng/ml during the first 3 months post transplant and 7-10 ng/ml thereafter; Etanercept 50 mg iv 1 hour before transplant and 25 mg s.c. on days 3, 7,and 10 post-transplant; Exenatide 5-mcg s.c. bid for 1 week, then 10 mcg bid for 6 months after each transplant