Under construction – not a live service
Sign in
Taking people in United StatesPhase 1

Tirzepatide and Stomach Emptying in Adults With Type 1 Diabetes and Excess Weight

Tests how tirzepatide affects stomach emptying in adults with type 1 diabetes and overweight.

Plain-language title generated from the registry record
Registry title: A Study of Tirzepatide (LY3298176) in Participants With Type 1 Diabetes Mellitus and Overweight or Obesity

Key facts

Where
Miami, United StatesSee the site
Phase
Phase 1

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 70 years old?

Source: NCT07803744, who can take part

Where in United States

  • Clinical Pharmacology of MiamiMiami, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Eli Lilly and Company
Trial code
NCT07803744
Record updated
23 September 2026
Original description
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.Read full original descriptionShow less

A Phase 1, Investigator- and Participant- Blinded, Randomized, Placebo-Controlled, Single-Dose Study to Investigate the Impact of Tirzepatide on Gastric Emptying in Adult Participants With Type 1 Diabetes Mellitus and Overweight or Obesity

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.

Inclusion: Have a diagnosis of type 1 diabetes mellitus (T1DM) and have been treated with insulin for at least 1 year prior to screening; Have a body mass index (BMI) greater than or equal to 25.0 kilograms per square meter (kg/m2) at screening; Are of stable weight, that is a self-reported change of 5 kg or less, for at least 90 days prior to screening.

Exclusion: Have undergone weight loss surgery such as gastric bypass (bariatric) surgery or restrictive bariatric surgery; Have known allergies or intolerance to acetaminophen, tirzepatide, or glucagon-like peptide-1 (GLP-1) receptor agonists; Participants who have a known clinically significant gastric emptying abnormality.

ClinicalTrials.gov NCT07803744