A Study of Tirzepatide (LY3298176) in Adult Participants in India With Either Type 2 Diabetes Mel… (NCT07438444) | Clinical Trial Compass
RecruitingPhase 4
A Study of Tirzepatide (LY3298176) in Adult Participants in India With Either Type 2 Diabetes Mellitus or Obesity
India344 participantsStarted 2026-02-27
Plain-language summary
The main purpose of this study is to measure the safety and efficacy of tirzepatide in adult participants in India who have type 2 diabetes or who have obesity or overweight without type 2 diabetes. Participation in the study will last about 46 weeks.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Participants with Type 2 Diabetes:
* Have had type 2 diabetes for at least one year
* Insulin naive
* Have HbA1c ≥7.5% and ≤10% at screening
* Have body mass index (BMI) ≥23 kilograms per square meter (kg/m2)
Participants with Obesity or Overweight without Type 2 Diabetes:
* Have a BMI
* Greater than or equal to 30 kg/m2 OR
* Greater than or equal to 27 kg/m2 AND previously diagnosed with at least one of the following weight-related comorbidities: high blood pressure, lipid disorder, obstructive sleep apnea, heart disease
Exclusion Criteria:
Participants with Type 2 Diabetes:
* Have type 1 diabetes
* Have had any of the following heart conditions within 6 months prior to screening:
* heart attack
* stroke
* hospitalization due to heart failure
* Have New York Heart Association Functional Classification Class III or IV congestive heart failure (CHF)
* Have type 2 diabetes along with morbid obesity and being considered for bariatric surgery or any other procedure intended for weight loss
Participants with Obesity or Overweight without Type 2 Diabetes:
* Have type 1 diabetes or type 2 diabetes
* Have a self-reported change in body weight greater than 5 kilograms (kg) (11 pounds) within 3 months prior to screening
* Have a prior or planned surgical treatment for obesity
* Have had any of the following heart conditions within 6 months prior to screening:
* heart attack
* stroke
* hospitalization due to heart failure
* Have New York H…
What they're measuring
1
Number of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug Administration
Timeframe: Baseline through Week 46
Trial details
NCT IDNCT07438444
SponsorEli Lilly and Company
Sponsor typeINDUSTRY
Study typeINTERVENTIONAL
Primary completion2027-10
Contact for this trial
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or