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Clinical Trial Details

Trial ID: L6324
Source ID: NCT04586907
Associated Drug: Ly3537021
Title: A Study of LY3537021 in Healthy Participants and Participants With Type 2 Diabetes Mellitus
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Healthy|Type 2 Diabetes Mellitus
Interventions: DRUG: LY3537021|DRUG: Placebo
Outcome Measures: Primary: Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration, A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module, Baseline through Day 119 (Part A) and Day 57 (Part B) | Secondary: Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3537021, PK: AUC of LY3537021, Predose Day 1 through Day 119 (Part A) and Day 57 (Part B)|PK: Maximum Concentration (Cmax) of LY3537021, PK: Cmax of LY3537021, Predose Day 1 through Day 119 (Part A) and Day 57 (Part B)
Sponsor/Collaborators: Sponsor: Eli Lilly and Company
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 85
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: BASIC_SCIENCE
Start Date: 2020-11-23
Completion Date: 2021-11-30
Results First Posted:
Last Update Posted: 2021-12-17
Locations: Lilly Centre for Clinical Pharmacology, Singapore, 138623, Singapore
URL: https://clinicaltrials.gov/show/NCT04586907