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Active, not recruiting Phase 3 Interventional

A Study to Learn About the Study Medicine (PF-08653944) in People With Obesity or Overweight and Type 2 Diabetes (T2D)

ClinicalTrials.gov ID: NCT07400653

Public ClinicalTrials.gov record NCT07400653. 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 Sep 1, 2026, 10:17 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

EVALUATING THE EFFICACY AND SAFETY OF MET097, A FULLY-BIASED ULTRA LONG-ACTING GLP-1RA, IN PEOPLE WITH OVERWEIGHT OR OBESITY AND TYPE 2 DIABETES: A PHASE 3, MULTI-CENTER RANDOMIZED PLACEBO-CONTROLLED TRIAL (VESPER-5)

Brief summary

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

The purpose of this clinical study is to learn about the safety and effects of the study medicine to help adults with obesity or overweight and type 2 diabetes lose weight. Being overweight or obese means carrying too much body weight. Type 2 diabetes is a condition where there is too much sugar in the blood. The study medicine is given by a shot under the skin in the belly area. The participants will be trained to do this at home once every week. About 660 out of 1000 adults will also receive the study medicine and about 330 out of 1000 adults will receive placebo. A placebo does not have any medicine in it but looks just like the medicine being studied. The investigators will compare the experiences of people receiving the study medicine to those of the people who do not. This will help us assess if the study medicine is safe and effective. People will take part in this study for about 21 months. During this time, they will have about 14 study visits at the site and 5 over the phone.

Study identification

NCT ID
NCT07400653
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
1,044 participants

Conditions and interventions

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
Feb 23, 2026
Primary completion
Oct 11, 2027
Completion
May 15, 2028
Last update posted
Jul 26, 2026

2026 – 2028

United States locations

U.S. sites
48
U.S. states
14
U.S. cities
44
Facility City State ZIP Site status
CenExel Anaheim Clinical Trials Anaheim California 92801
Alliance Research Institute Canoga Park California 91304
Core Healthcare Group Cerritos California 90703
CenExel CNS - Collaborative Neuroscience Research Los Alamitos California 90720
Catalina Research Institute, LLC Montclair California 91763
Cure Clinical Research Orange California 92866
CenExel CIT Riverside California 92506
Lundquist Institute for Biomedical Innovation at Harbor- UCLA Medical Center Torrance California 90502
CenExcel Rocky Mountain Clinical Research, LLC Englewood Colorado 80113
CenExel Denver CO (Rocky Mountain Clinical Research) Englewood Colorado 80113
Neuro-Sight Vision Care Lakewood Colorado 80226
AMR Clinical Fort Myers Florida 33912
Pedro P. Ylisastigui, MD Fort Myers Florida 33912
Private Practice Adjacent to For Eyes Optical Hialeah Florida 33014
Miami Eye Institute Hollywood Florida 33024
Research Centers of America Hollywood Florida 33024
Future Medical Research (Civia Health) Longwood Florida 32750
Advanced Clinical Research Miami Florida 33156
Indago Research & Health Center, Inc Miami Lakes Florida 33016
Optimal Research Sites, LLC Orange City Florida 32763
Oviedo Medical Research Oviedo Florida 32765
CenExel FCR - ForCare Clinical Research Tampa Florida 33613
DelRicht Research Atlanta Georgia 30329
CenExel iResearch, LLC Decatur Georgia 30030
CenExel iResearch, LLC Savannah Georgia 31405
Patient First Clinical Trials (PFCTRIALS) Lutherville Maryland 21093
DelRicht Research Springfield Missouri 65807
Quality Clinical Research Inc Omaha Nebraska 68114
Primary clinical Research Papillion Nebraska 68046
Hassman Research Institute Marlton New Jersey 08053
Forum Health_Cary (Civia) Cary North Carolina 27511
Eximia EquiHealth Research Durham North Carolina 27704
Sahana Optometry PLLC dba Family Eye Wellness Holly Springs North Carolina 27540
Burke Primary Care Morganton North Carolina 28655
Eximia Research - NC, LLC Raleigh North Carolina 27607
Tribe Clinical Research LLC.- Greenville Greenville South Carolina 29607
Tribe Clinical Research LLC. - Spartanburg Spartanburg South Carolina 29301
Civia Health Goodlettsville Goodlettsville Tennessee 37072
Civia Health Nashville La Vergne Tennessee 37086
Amarillo Medical Specialists LLP Amarillo Texas 79124
Forum Austin (Civia Health) Austin Texas 78578
GLRI El Paso Research El Paso Texas 79936
Cardiovascular Specialists of Willowbrook Houston Texas 77070
Dallas Clinical Research Center (Pillar Clinical Research) Richardson Texas 75080
Pantheon Clinical Research Bountiful Utah 84010
CenExel Salt Lake City UT (JBR Clinical Research) Salt Lake City Utah 84107
Murray Vision Center PC Salt Lake City Utah 84107
ERA Health Research Redmond Washington 98052

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 135 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07400653, 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 Jul 26, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07400653 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →