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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

Full criteria on ClinicalTrials.gov

Sites (17)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Northwest Clinical Research Center
Coordinator of this site? Confirm its status
BellevueUnited StatesUnknown status
CTI Clinical Research Center
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CincinnatiUnited StatesUnknown status
South Texas Clinical Research
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Corpus ChristiUnited StatesUnknown status
Velocity Clinical Research, Dallas
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DallasUnited StatesUnknown status
Lillestol Research
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FargoUnited StatesUnknown status
Velocity Clinical Research, Gardena
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GardenaUnited StatesUnknown status
Juno Research
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HoustonUnited StatesUnknown status
Irvine Clinical Research
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IrvineUnited StatesUnknown status
Velocity Clinical Research, Los Angeles
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Los AngelesUnited StatesUnknown status
Hassman Research Institute Marlton Site
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MarltonUnited StatesUnknown status
Tandem Clinical Research
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MarreroUnited StatesUnknown status
Solaris Clinical Research
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MeridianUnited StatesUnknown status
Velocity Clinical Research, New Orleans
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New OrleansUnited StatesUnknown status
Velocity Clinical Research - North Hollywood
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North HollywoodUnited StatesUnknown status
Velocity Clinical Research, Santa Ana
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Santa AnaUnited StatesUnknown status
Velocity Clinical Research, Panorama City
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Van NuysUnited StatesUnknown status
Diablo Clinical Research, Inc.
Coordinator of this site? Confirm its status
Walnut CreekUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.