LivingGLP1
Study S000016

A Multiple-Dose Drug-Drug Interaction Study to Determine the Effect of LY3437943 on Drug Metabolizing Enzymes

Registration

Registration
NCT05445232
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
32
Start
2022-07-08
Primary completion
2023-02-24
Lead sponsor
Eli Lilly and Company
Conditions
Obesity
Interventions
DRUG:LY3437943; DRUG:Midazolam; DRUG:Warfarin; DRUG:Caffeine
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1I-MC-GZBI

Registered primary outcomes

  • Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve From Zero to Infinity (AUC[0-∞]) of Midazolam [Predose up to 24 hours postdose]
  • PK: Maximum Observed Concentration (Cmax) of Midazolam [Predose up to 24 hours postdose]
  • PK: AUC[0-∞] of Warfarin [Predose up to 96 hours postdose]
  • PK: Cmax of Warfarin [Predose up to 96 hours postdose]
  • PK: AUC[0-∞] of Caffeine [Predose up to 48 hours postdose]
  • PK: Cmax of Caffeine [Predose up to 48 hours postdose]

Linked records (0)

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