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Clinical Trial Details

Trial ID: L3655
Source ID: NCT00532610
Associated Drug: Gsk189075
Title: A Study to Compare the Effect on Heart Rhythm of 3 Days of GSK189075, Placebo, or Moxifloxacin in Healthy Adults
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Type 2 Diabetes Mellitus|Diabetes Mellitus, Type 2
Interventions: DRUG: GSK189075
Outcome Measures: Primary: Continuous holter monitor & ECG each treatment period:, Days 1 & 3 | Secondary: Drug plasma levels each treatment period:, Days 2 & 3|Safety ECG, labs, vital signs & adverse events:, each treatment period & follow-up|Day 3 change from baseline in QTcB, QTci, QT, and HR.|Blood drug levels of GSK189075 (pro-drug), GSK189074 (active entity), GSK279782 (active metabolite), GSK333081 (metabolite; may be analyzed as indicated by data from the dose escalation study) and moxifloxacin.|12-lead ECGs, vital signs, adverse events, and clinical laboratory tests.
Sponsor/Collaborators: Sponsor: GlaxoSmithKline
Gender: ALL
Age: ADULT
Phases: PHASE1
Enrollment: 78
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: DOUBLE|Primary Purpose: TREATMENT
Start Date: 2007-09
Completion Date: 2008-02
Results First Posted:
Last Update Posted: 2012-03-19
Locations: GSK Investigational Site, Madison, Wisconsin, 53704, United States
URL: https://clinicaltrials.gov/show/NCT00532610