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A Phase II Randomized, Double-Blind, Dose-Ranging Study to Determine the Efficacy, Safety, Tolerability & Pharmacokinetics of RO 205-2349 in Patients With Type 2 Diabetes Mellitus

NCT00057304 Phase 2 COMPLETED

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.

Details

Lead sponsorHoffmann-La Roche
PhasePhase 2
StatusCOMPLETED
Enrolment190
Start date2003-06
Completion2004-03

Conditions

Interventions

Countries

United States, Bulgaria, Estonia, Mexico, Panama, Puerto Rico, Romania, Switzerland, United Kingdom