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Clinical Trial Details

Trial ID: L3896
Source ID: NCT04823208
Associated Drug: Ly3437943
Title: A Study of LY3437943 in Japanese Participants With Type 2 Diabetes Mellitus (T2DM)
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Diabetes Mellitus, Type 2
Interventions: DRUG: LY3437943|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 106 | Secondary: Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3437943, PK: Cmax of LY3437943, Predose on Day 1 through Day 81|PK: Area Under the Concentration Versus Time Curve (AUC) of LY3437943, PK: AUC of LY3437943, Predose on Day 1 through Day 81|Change from Baseline in Mean Daily Plasma Glucose (PG), Change from baseline in mean daily PG from 6-point PG profile, Baseline through Day 80|Change from Baseline in Glycated Hemoglobin (HbA1c), Change from Baseline in HbA1c, Baseline through Day 78|Change from Baseline in Fasting Glucose, Change from Baseline in Fasting Glucose, Baseline through Day 78|Change from Baseline in Body Weight, Change from Baseline in Body Weight, Baseline through Day 78
Sponsor/Collaborators: Sponsor: Eli Lilly and Company
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 64
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: BASIC_SCIENCE
Start Date: 2021-05-24
Completion Date: 2022-06-23
Results First Posted:
Last Update Posted: 2022-08-22
Locations: Medical Corporation Heishinkai OCROM Clinic, Suita-shi, Osaka, 565-0853, Japan|P-one clinic, Hachioji, Tokyo, 192-0071, Japan|Clinical Research Hospital Tokyo, Shinjuku-ku, Tokyo, 162-0053, Japan|Yokohama Minoru Clinic, Yokohama, 232-0064, Japan
URL: https://clinicaltrials.gov/show/NCT04823208