drugset / Trial / NCT00886821

A Safety and Pharmacokinetic Study of CVX-096 in Type 2 Diabetics

NCT00886821 ↗

Phase 1 Completed 114 enrolled Pfizer
RandomizedSingle-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine safety and tolerability of CVX-096 in adult, type 2 diabetic patients.

Timeline

Start
2008-10
Primary completion
2011-06
Completion
2011-06

Drugs

EvaluationDrugModalityDoseRoute
Subject CVX-096 Unknown 0.1 mg Subcutaneous
Subject CVX-096 Unknown 36 mg Subcutaneous