CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 6 enrolled
Drug / intervention
14C Tirzepatidedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04311424
NCT04311424Phase 1Completed

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

Eli Lilly and Company·interventional·Posted Mar 17, 2020·Updated Mar 24, 2023

In Brief

A Phase 1 clinical trial evaluating 14C Tirzepatide for Healthy. Completed, enrolled 6 participants across 1 site.

Detailed Summary

The purpose of this study is to look at how much tirzepatide gets into the bloodstream and how long the body takes to get rid of it. This study will involve a single dose of 14C radiolabelled tirzepatide. This means that a radioactive tracer substance, C14, will be incorporated into the study drug to investigate the study drug and its breakdown products and to find out how much of these pass from blood into urine, feces and expired air. Screening is required within 28 days prior to the start of the study. For each participant, the total duration of the clinical trial will be approximately 15 weeks, including screening.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited Kingdom
Collaborators--

Timeline

Phase 1CompletedFinished
202120222023202420252026
First PostedMar 17, 2020
Enrollment StartJul 28, 2020
Primary CompletionOct 2, 2020
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 6.3 years ago

Interventions

14C Tirzepatidedrug

Administered SC.