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Completed Phase 3 Interventional

A Study of LY3298176 (Tirzepatide) For the Maintenance of Body Weight Reduction in Participants Who Have Obesity or Overweight With Weight-Related Comorbidities

ClinicalTrials.gov ID: NCT06047548

Public ClinicalTrials.gov record NCT06047548. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 11, 2026, 9:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3b, Randomized Controlled Study to Evaluate the Efficacy and Safety of Tirzepatide Once Weekly 5 mg and/or Maximum Tolerated Dose Versus Placebo for Maintenance of Body Weight Reduction in Participants Who Have Obesity or Overweight With Weight-Related Comorbidities (SURMOUNT-MAINTAIN)

Study identification

NCT ID
NCT06047548
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
441 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Tirzepatide Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 19, 2023
Primary completion
Jan 19, 2026
Completion
Jan 19, 2026
Last update posted
Mar 24, 2026

2023 – 2026

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Cahaba Research - Pelham Pelham Alabama 35124
Velocity Clinical Research, Westlake Los Angeles California 90057
Southern California Dermatology, Inc. Santa Ana California 92701
Encompass Clinical Research Spring Valley California 91978
New Horizon Research Center Miami Florida 33165
Oviedo Medical Research Oviedo Florida 32765
Rophe Adult and Pediatric Medicine/SKYCRNG Union City Georgia 30291
East-West Medical Research Institute Honolulu Hawaii 96814
Rocky Mountain Clinical Research Idaho Falls Idaho 83404
Asha Clinical Research - Munster Hammond Indiana 46324
Iowa Diabetes and Endocrinology Research Center West Des Moines Iowa 50265
L-MARC Research Center Louisville Kentucky 40213
Prime Health and Wellness/SKYCRNG Fayette Mississippi 39069
Alliance for Multispecialty Research, LLC Norman Oklahoma 73069
WR-Clinsearch, LLC Chattanooga Tennessee 37397
The University of Texas Health Science Center at Houston Bellaire Texas 77401
Velocity Clinical Research, Dallas Dallas Texas 75230
Southern Endocrinology Associates Mesquite Texas 75149
Pinnacle Clinical Research San Antonio Texas 78229
Consano Clinical Research, LLC Shavano Park Texas 78231

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06047548, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 24, 2026 · Synced May 11, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06047548 live on ClinicalTrials.gov.

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