LivingGLP1
Study S002235

A Single-Group, Open-Label, Single-Period, Phase 1 Study to Determine the Absolute Bioavailability of LY3502970 in Healthy Participants

Registration

Registration
NCT06085482
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
10
Start
2023-10-19
Primary completion
2024-01-05
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:LY3502970; DRUG:[14C]-LY3502970
Results posted
TRUE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J2A-MC-GZGO

Registered primary outcomes

  • Pharmacokinetics (PK): Absolute Bioavailability of LY3502970 [Pre-oral dose, 0.5, 1, 2, 4, 6, 6.5, 7, 8, 10, 12, 16, 24, 36, 48, 72, 96, 120 hours post-oral dose; 0 (immediately after IV dosing), 2, 5, 10, 15 minutes and 0.5, 1, 2, 4, 6, 10, 18, 30, 42, 66, 90, 114, 138, 162, 186 hours post-IV dose.]

Linked records (0)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.

No records link to this registration yet.