LivingGLP1
Study S001835

A Phase 1, Open-Label, Multiple-Dose Study to Investigate the Comparability of the Pharmacokinetics of Orforglipron (LY3502970) Single Capsule and Multiple Capsules in Healthy Participants

Registration

Registration
NCT06692348
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
86
Start
2024-12-13
Primary completion
2025-06-09
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:Orforglipron
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J2A-JE-GZPM

Registered primary outcomes

  • Pharmacokinetics (PK): Steady-state Area Under the Concentration Versus Time Curve (AUC) of Orforglipron (Fasted State) [Week 3 Through Week 16]
  • PK: Steady-state Maximum Concentration (Cmax) of Orforglipron (Fasted State) [Week 3 Through Week 16]
  • PK: Steady-state AUC of Orforglipron (Fed State) [Week 3 Through Week 16]
  • PK: Steady-state Cmax of Orforglipron (Fed State) [Week 3 Through Week 16]

Linked records (0)

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