LivingGLP1
Study S001813

A Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3841136 Monotherapy, and LY3841136 in Combination With Tirzepatide, in Japanese Participants With Obesity or Overweight

Registration

Registration
NCT06297616
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
128
Start
2024-04-15
Primary completion
2025-11-21
Lead sponsor
Eli Lilly and Company
Conditions
Obesity; Overweight
Interventions
DRUG:LY3841136; DRUG:LY3841136-Placebo; DRUG:Tirzepatide; DRUG:Tirzepatide-Placebo
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J3R-JE-YDAB

Registered primary outcomes

  • Part A: Number of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug Administration at Week 22 [Baseline through Week 22]
  • Part B: Number of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug Administration at Week 34 [Baseline through Week 34]

Linked records (0)

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