A Study of Investigational Dulaglutide Doses in Participants With Type 2 Diabetes on Metformin Monotherapy
Part of paid clinical trials in Glendale, California.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT02973100
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Dulaglutide — DRUGAdministered SC
- Placebo — DRUGAdministered SC
Study Details
The purpose of this study is to evaluate the efficacy and safety of investigational doses of dulaglutide in participants with type 2 diabetes on metformin monotherapy.
Key Dates
- Start date
- Dec 31, 2016
- Status verified
- Sep 2019
- Primary completion
- Jul 15, 2017
- Completion
- Aug 14, 2017
Study Design
- Enrollment
- 318 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Dulaglutide 4.5mg4.5mg of Dulaglutide administered subcutaneously (SC)
- Experimental: Dulaglutide 3.0mg3.0mg of Dulaglutide administered SC
- Active Comparator: Dulaglutide 1.5mg1.5mg of Dulaglutide administered SC
- Placebo Comparator: PlaceboPlacebo administered SC
Primary Outcome Measure
Change From Baseline in Hemoglobin A1c (HbA1c) [ Time Frame: Baseline, Week 18 ]
Locations (38)
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