LivingGLP1
Study S002309

Disposition of [¹⁴C]-LY3502970 Following Oral Administration in Healthy Male Participants

Registration

Registration
NCT04680767
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
6
Start
2021-03-29
Primary completion
2021-07-03
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:[¹⁴C]-LY3502970
Results posted
TRUE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J2A-MC-GZGF

Registered primary outcomes

  • Feces Excretion of LY3502970 Radioactivity Over Time Expressed as a Percentage of the Total Radioactive Dose Administered [0, 24, 48, 72, 96, 120, 144, 168, 192, 216, 240, 264, 288, 312, 336, 360, and 384 hours (h) postdose]
  • Urinary Excretion of LY3502970 Radioactivity Over Time Expressed as a Percentage of the Total Radioactive Dose Administered [0, 24, 48, 72, 96, 120, 144, 168, 192, 216, 240, 264, 288, 312, 336, 360, and 384 hours (h) postdose]

Linked records (0)

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