LivingGLP1
Study S001347

A Single- and Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3502970 in Healthy Subjects

Registration

Registration
NCT03929744
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
133
Start
2019-06-12
Primary completion
2020-11-02
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:LY3502970; DRUG:Placebo; DRUG:Atorvastatin; DRUG:Simvastatin; DRUG:Midazolam
Results posted
TRUE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J2A-MC-GZGA

Registered primary outcomes

  • Parts A and B: Number of Participants With One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug [Baseline through Follow-up (up to Day 42)]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0004741Effect of Food Consumption on the Pharmacokinetics, Safety, and Tolerability of Once-Daily Orally Administered Orforglipron (LY3502970), a Non-peptide GLP-1 Receptor Agonist.
Ma X, Diabetes therapy : research, treatment and education of diabetes and related disorders
2024Randomized trialPMID 38402332DOIcites ClinicalTrials.gov:NCT03929744; registry reference DERIVED:38402332
R0055527336-OR: A First-in-Human Single- and Multiple-Ascending Dose Study Evaluating Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of a Novel Oral Nonpeptide GLP-1 Receptor Agonist in Healthy Subjects
EDWARD J. PRATT, Diabetes
2022Randomized trialDOIcites ClinicalTrials.gov:NCT03929744