drugset / Trial / NCT01176097

To Assess Safety, Tolerability, Pharmacokinetics/Pharmacodynamics and the Effect of Fasting After Single Oral Doses of AZD5658 in Type 2 Diabetes

NCT01176097 ↗

Phase 1 Completed 24 enrolled AstraZeneca
RandomizedSingle-groupSingle-blindTreatment

Summary

The purpose of this study is to investigate the safety and tolerability of AZD5658 following ascending single oral doses in Type 2 Diabetics. It will also estimate the maximum tolerated dose.

Timeline

Start
2010-07
Primary completion
2011-02
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator AZD5658 Unknown — Oral