drugset / Trial / NCT01681290

Safety and Efficacy of CBX129801 in Patients With Type 1 Diabetes

NCT01681290 ↗

Phase 2 Completed 250 enrolled Cebix Incorporated
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to determine the beneficial effects of CBX129801 (PEGylated synthetic human C-peptide) following weekly subcutaneous administration for 12 months in type 1 diabetes mellitus patients (T1DM) with mild to moderate diabetic peripheral neuropathy (DPN).

Timeline

Start
2012-10
Primary completion
2014-11
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Subject CBX129801 Peptide 0.8 mg Subcutaneous
Subject CBX129801 Peptide 2.4 mg Subcutaneous