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Life sciences · Phase 1 Trial
ClinicalTrials.gov · September 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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Registry record from ClinicalTrials.gov (NCT07803744). This is a study registration, not published results. Lead sponsor: Eli Lilly and Company. Recruitment status: RECRUITING. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 18 participants (ESTIMATED). Conditions: Diabetes Mellitus, Type 1, Overweight, Obesity. Interventions: DRUG: Tirzepatide; DRUG: Acetaminophen; DRUG: Placebo. Primary outcome measures: Pharmacokinetics (PK): Time of Maximum Observed Drug Concentration (Tmax) of Acetaminophen , Predose on Day 1 through 36 hours post dose; PK: Area Under the Concentration Versus Time Curve from Time Zero to Time t (AUC0-tlast) of Acetaminophen , Predose on Day 1 through 36 hours post dose; PK: Maximum Observed Drug Concentration (Cmax) of Acetaminophen , Predose on Day 1 through 36 hours post dose. Brief summary: The main purpose of this study is to learn more how tirzepatide affects stomach emptying in participants with Type 1 Diabetes Mellitus (T1DM) and overweight or obesity. Participation in this study will last about 8 weeks, including screening and follow-up.