LivingGLP1
Study S001597

A Double-blind, Placebo-controlled Titration Study to Investigate the Tolerability, Safety and Pharmacodynamic Profile of a GLP-1 Analogue in Patients With Type 2 Diabetes Mellitus Treated With a Stable Dose of Metformin.

Registration

Registration
NCT00460941
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
133
Start
2007-04
Primary completion
2008-01
Lead sponsor
Hoffmann-La Roche
Conditions
Diabetes Mellitus Type 2
Interventions
DRUG:Placebo; DRUG:Taspoglutide 20mg; DRUG:Taspoglutide 20mg-30mg; DRUG:Taspoglutide 20mg-40mg
Results posted
FALSE

Registered primary outcomes

  • Percentage of patients withdrawn because of gastrointestinal effects [Week 9]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0021258Safety and tolerability of high doses of taspoglutide, a once-weekly human GLP-1 analogue, in diabetic patients treated with metformin: a randomized double-blind placebo-controlled study.
Ratner R, Diabetic medicine : a journal of the British Diabetic Association
2010Randomized trialPMID 20536952DOIcites ClinicalTrials.gov:NCT00460941; registry reference DERIVED:20536952