drugset / Trial / NCT01293461

Safety and Pharmacokinetics of CBX129801 in Patients With Type 1 Diabetes

NCT01293461 ↗

Phase 1/2 Completed 72 enrolled Cebix Incorporated
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess safety and tolerability and determine the pharmacokinetics of subcutaneous single and multiple (up to 12) dose administration of CBX129801 (long-acting synthetic C-peptide) in type 1 diabetes patients.

Timeline

Start
2011-04
Primary completion
2012-08
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject CBX129801 Peptide — Subcutaneous