LivingGLP1
Study S000678

A Dose-Escalation Treatment, Phase 1, Investigator- and Participant-Blind, Placebo-controlled Study to Investigate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of LY3457263 in Combination With Tirzepatide in Overweight or Obese Participants

Registration

Registration
NCT05582096
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
38
Start
2022-11-11
Primary completion
2023-06-08
Lead sponsor
Eli Lilly and Company
Conditions
Overweight; Obesity
Interventions
DRUG:LY3457263; DRUG:Tirzepatide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1R-MC-GZFC

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 11 weeks]

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