LivingGLP1
Study S000177

Effect of Injection Site on the Relative Bioavailability of a Single Dose of Tirzepatide in Subjects With Low and High Body Mass Indices

Registration

Registration
NCT04050670
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
54
Start
2019-09-13
Primary completion
2020-04-03
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:Tirzepatide
Results posted
TRUE
Individual participant data sharing
NO
Secondary identifiers
OTHER:I8F-MC-GPHI

Registered primary outcomes

  • Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve of Tirzepatide From Time Zero to Infinity (AUC[0-∞]) [Predose, 8, 12, 24, 36, 48, 72, 96, 120, 144, 168, 336, 480 hours post dose]
  • PK: Maximum Concentration (Cmax) of Tirzepatide [Predose, 8, 12, 24, 36, 48, 72, 96, 120, 144, 168, 336, 480 hours post dose]

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