drugset / Trial / NCT00057304

Study to Determine the Efficacy, Safety, Tolerability & Pharmacokinetics of RO 205-2349 in Patients With Type 2 Diabetes Mellitus

NCT00057304 ↗

Phase 2 Completed 190 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of the study is to determine the dose(s) of Ro 205-2349 which, when compared to placebo, are efficacious, safe and tolerable in improving glycemic control in patients with type 2 diabetes. Doses of 2 to 5 mg/day will be studied.

Timeline

Start
2003-06
Primary completion
2004-03
Completion
2004-03

Drugs

EvaluationDrugModalityDoseRoute
Subject RO 205-2349 Unknown 2 mg —
Subject RO 205-2349 Unknown 5 mg —

Indications