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Completed Phase 3 Interventional

A Study of Orforglipron for the Maintenance of Body Weight Reduction in Participants Who Have Obesity or Overweight With Weight-Related Comorbidities (ATTAIN-MAINTAIN)

ClinicalTrials.gov ID: NCT06584916

Public ClinicalTrials.gov record NCT06584916. 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 Oct 23, 2026, 3:42 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, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Orforglipron Once Daily Versus Placebo for Maintenance of Body Weight Reduction in Participants Who Have Obesity or Overweight With Weight-Related Comorbidities

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main purpose of this study is to evaluate the efficacy and safety of orforglipron on maintenance of body weight reduction in participants who previously completed treatment with injectable tirzepatide (Zepbound) or injectable semaglutide (Wegovy) in the SURMOUNT-5 trial (NCT05822830).

Study identification

NCT ID
NCT06584916
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
376 participants

Conditions and interventions

Interventions

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 13, 2024 (Actual)
Primary completion
Nov 21, 2025 (Actual)
Completion
Nov 21, 2025 (Actual)
Last update posted
Jun 4, 2026

2024 – 2025

United States locations

U.S. sites
27
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Cahaba Research Birmingham Alabama 35242 —
Cahaba Research - Pelham Pelham Alabama 35124 —
Southern California Dermatology, Inc. Santa Ana California 92701 —
Encompass Clinical Research Spring Valley California 91978 —
University Clinical Investigators, Inc. Tustin California 92780 —
New Horizon Research Center Miami Florida 33165 —
Rophe Adult and Pediatric Medicine/SKYCRNG Union City Georgia 30291 —
Rocky Mountain Clinical Research Idaho Falls Idaho 83404 —
Iowa Diabetes and Endocrinology Research Center West Des Moines Iowa 50265 —
L-MARC Research Center Louisville Kentucky 40213 —
Arcturus Healthcare , PLC, Troy Internal Medicine Research Division Troy Michigan 48098 —
Prime Health and Wellness/SKYCRNG Fayette Mississippi 39069 —
StudyMetrix Research City of Saint Peters Missouri 63303 —
Palm Research Center Tenaya Las Vegas Nevada 89128 —
Palm Research Center Sunset Las Vegas Nevada 89148 —
Weill Cornell Medical College New York New York 10021 —
PharmQuest Life Sciences, LLC Greensboro North Carolina 27408 —
Lillestol Research Fargo North Dakota 58104 —
Alliance for Multispecialty Research, LLC Norman Oklahoma 73069 —
Tribe Clinical Research, LLC Greenville South Carolina 29607 —
WR-Clinsearch, LLC Chattanooga Tennessee 37421 —
The University of Texas Health Science Center at Houston Bellaire Texas 77401 —
Velocity Clinical Research, Dallas Dallas Texas 75230 —
North Texas Endocrine Center Dallas Texas 75231 —
Biopharma Informatic, LLC Houston Texas 77043 —
PlanIt Research, PLLC Houston Texas 77079 —
Southern Endocrinology Associates Mesquite Texas 75149 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06584916, 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 Jun 4, 2026 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06584916 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →