LivingGLP1
Study S000166

A Phase 1, Double-Blind, Randomized, Placebo-Controlled, Study to Evaluate the Safety and Tolerability of LY3537021 When Combined With GLP-1 Receptor Agonist in Healthy Participants

Registration

Registration
NCT05444569
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
47
Start
2022-08-08
Primary completion
2023-02-24
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:LY3537021; DRUG:Liraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J2R-MC-YAAC

Registered primary outcomes

  • 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 [Baseline up to Week 22]

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