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Clinical Trial Details

Trial ID: L7227
Source ID: NCT05377333
Associated Drug: Ly3457263
Title: A Study of LY3457263 Alone and in Combination With Dulaglutide (LY2189265) in Participants With Type 2 Diabetes
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Diabetes Mellitus, Type 2
Interventions: DRUG: LY3457263|DRUG: Placebo|DRUG: Dulaglutide
Outcome Measures: Primary: Number of Participants with One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration, A summary of TEAEs, SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module, Predose up to 16 weeks | Secondary: PK: Area Under the Concentration Versus Time Curve (AUC) of LY3457263, PK: AUC of LY3457263, Pre-dose on Day 1 up to 85 days post-dose
Sponsor/Collaborators: Sponsor: Eli Lilly and Company
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 94
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: BASIC_SCIENCE
Start Date: 2022-06-02
Completion Date: 2023-11-22
Results First Posted:
Last Update Posted: 2024-01-11
Locations: Pinnacle Research Group, LLC, Anniston, Alabama, 36207, United States|CenExel ACT, Anaheim, California, 92801, United States|Qps-Mra, Llc, South Miami, Florida, 33143, United States|Atlanta Center of Medical Research, Atlanta, Georgia, 30331 2012, United States|CenExel-HRI, Berlin, New Jersey, 08009, United States
URL: https://clinicaltrials.gov/show/NCT05377333