LivingGLP1
Study S000167

Disposition of [14C]-LY3437943 Following Subcutaneous Administration in Healthy Male Participants

Registration

Registration
NCT05757531
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
7
Start
2023-03-17
Primary completion
2023-06-23
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:[¹⁴C]-LY3437943
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1I-MC-GZBG

Registered primary outcomes

  • Urinary Excretion of LY3437943 Radioactivity Over Time Expressed as a Percentage of the Total Radioactive Dose Administered [Predose up to 63 days post dose]
  • Fecal Excretion of LY3437943 Radioactivity Over Time Expressed as a Percentage of the Total Radioactive Dose Administered [Predose up to 63 days post dose]

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