NCT06373146CompletedPhase 2
A Study of Tirzepatide (LY3298176) Plus Mibavademab Compared With Tirzepatide Alone in Adult Participants With Obesity
A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Proof-of-Concept Study of Once-Weekly Tirzepatide Plus Mibavademab Compared With Tirzepatide Alone in Adult Participants With Obesity
Source: ClinicalTrials.gov · Last updated 6 May 2026
Brief summary (registry, in English)
The main purpose of this study is to determine if combining tirzepatide with mibavademab will result in more weight loss in adult participants than tirzepatide alone. The study will last about 74 weeks and may include up to 19 visits.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 392 (actual)
- First submitted
- 16 Apr 2024
- Start date
- 24 Apr 2024
- Primary completion date
- 15 Dec 2025
- Lead sponsor
- Eli Lilly and Company
- Diseases
- Obesity
- NCT number
- NCT06373146
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 392
- From 24 Apr 2024 to the primary completion date, 15 Dec 2025
- 17 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Have a self-reported change (increase or decrease) in body weight \>5 kilogram (kg) within 3 months prior to screening
Other illness
- Have a history of diabetes mellitus, including Type 1 Diabetes Mellitus (T1DM) or Type 2 Diabetes Mellitus (T2DM), history of ketoacidosis, or hyperosmolar state/coma
- Have a family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia (MEN) syndrome type 2
- Have acute or chronic hepatitis
- Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years
Who the study is looking for
- Have a body mass index (BMI) of ≥30 kilogram/square meter (kg/m²) and ≤40 kg/m²
- Willing to learn how to self-inject study intervention (visually impaired persons who are not able to perform the injections must have the assistance of a sighted individual trained to inject the study intervention; persons with physical limitations who are not able to perform the injections must have the assistance of an individual trained to inject the study intervention)
- Male or female contraceptive use by participant should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (17)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Northwest Clinical Research Center Coordinator of this site? Confirm its status | Bellevue | United States | Unknown status |
| CTI Clinical Research Center Coordinator of this site? Confirm its status | Cincinnati | United States | Unknown status |
| South Texas Clinical Research Coordinator of this site? Confirm its status | Corpus Christi | United States | Unknown status |
| Velocity Clinical Research, Dallas Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| Lillestol Research Coordinator of this site? Confirm its status | Fargo | United States | Unknown status |
| Velocity Clinical Research, Gardena Coordinator of this site? Confirm its status | Gardena | United States | Unknown status |
| Juno Research Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| Irvine Clinical Research Coordinator of this site? Confirm its status | Irvine | United States | Unknown status |
| Velocity Clinical Research, Los Angeles Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Hassman Research Institute Marlton Site Coordinator of this site? Confirm its status | Marlton | United States | Unknown status |
| Tandem Clinical Research Coordinator of this site? Confirm its status | Marrero | United States | Unknown status |
| Solaris Clinical Research Coordinator of this site? Confirm its status | Meridian | United States | Unknown status |
| Velocity Clinical Research, New Orleans Coordinator of this site? Confirm its status | New Orleans | United States | Unknown status |
| Velocity Clinical Research - North Hollywood Coordinator of this site? Confirm its status | North Hollywood | United States | Unknown status |
| Velocity Clinical Research, Santa Ana Coordinator of this site? Confirm its status | Santa Ana | United States | Unknown status |
| Velocity Clinical Research, Panorama City Coordinator of this site? Confirm its status | Van Nuys | United States | Unknown status |
| Diablo Clinical Research, Inc. Coordinator of this site? Confirm its status | Walnut Creek | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.