LivingGLP1
Study S001099

Disposition of [14C]-Tirzepatide Following Subcutaneous Administration in Healthy Male Subjects

Registration

Registration
NCT04311424
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
6
Start
2020-07-28
Primary completion
2020-10-02
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:14C Tirzepatide
Results posted
TRUE
Individual participant data sharing
NO
Secondary identifiers
OTHER:I8F-MC-GPHX; EUDRACT_NUMBER:2019-003664-44; NIH:2019

Registered primary outcomes

  • Urinary Excretion of Tirzepatide Radioactivity Over Time Expressed As A Percentage of the Total Radioactive Dose Administered [Pre-dose and up to 63 days post-dose]
  • Fecal Excretion of Tirzepatide Radioactivity Over Time Expressed As A Percentage of the Total Radioactive Dose Administered [Pre-dose and up to 63 days post-dose]

Linked records (0)

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