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A Study to Learn About the Study Medicine Called Berobenatide (PF-08653944) in People With Overweight or Obesity

RecruitingPhase 3

A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO ASSESS THE EFFICACY AND SAFETY OF ONCE-MONTHLY PF-08653944 IN ADULTS WITH OVERWEIGHT OR OBESITY (VESPER-6)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Aged ≥18 years.
* BMI of: ≥30 kg/m2 or ≥27.0 kg/m2 to \<30.0 kg/m2 and must have at least 1 of the following weight-related co-morbidities: hypertension, dyslipidemia, obstructive sleep apnea, cardiovascular disease, or T2D.

Exclusion Criteria:

* Have a self-reported body weight change greater than 5% within 90 days prior to Screening.
* Diagnosis of type 1 diabetes or any other form of diabetes other than T2D.
* History of acute or chronic pancreatitis.
* Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN-2).

About the study

The purpose of this clinical study is to learn about the effects and safety of berobenatide (PF-08653944). This may help people with overweight or obesity lose weight. People in this study may also have type 2 diabetes.

About 950 adults will be in this study. Berobenatide will be compared to a placebo. A placebo does not have any medicine in it but looks just like the medicine being studied. Berobenatide or placebo is given by a shot under the skin in the belly area. The objective of the study is to compare the experiences of people receiving berobenatide to those of the people who do not to assess if the study medicine is effective and safe.

People will take part in this study for about 20 months. During this time, they will have about 15 study visits at the site. They will also have 2 study visits over the phone.

What is being tested

Sponsor: Pfizer · Participants: 954 · Started: Jun 10, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07595549

Locations in the U.S.

CaliforniaSan Fernando Valley Health Institute, Canoga Park
Headlands Research California, LLC, Escondido
ImmuniMet, LLC, Modesto
Clinical Trials Research, Sacramento
University Clinical Investigators, Inc., Tustin
Diablo Clinical Research, Inc., Walnut Creek
Southern California Retina Specialists, West Hills
FloridaNature Coast Clinical Research, Crystal River
West Coast Eye Institute, Lecanto
South Broward Research, Miramar
Suncoast Clinical Research, Inc., New Port Richey
West Coast Medical Associates, New Port Richey
Center for Diabetes, Obesity and Metabolism Inc, Pembroke Pines
IllinoisCedar Crosse Research Center, Chicago
Northwestern University, Chicago
Endeavor Health - Family Medicine Administration, Evanston
Endeavor Health- Endocrinology Research, Skokie
IndianaMediSphere Medical Research Center, LLC, Evansville
KentuckyMonroe Biomedical Research, Louisville
MarylandAscension Saint Agnes Heart Care, Baltimore
MichiganAa Mrc Llc, Flint
NebraskaUniversity Of Nebraska Medical Center, Omaha
New MexicoAlbuquerque Clinical Trials, Inc., Albuquerque
New YorkWeill Cornell Medicine - Comprehensive Weight Control Center, New York
Rochester Clinical Research, LLC, Rochester
North CarolinaMedication Management, LLC, Greensboro
Accellacare - Wilmington, Wilmington
Jeffrey Coleman, OD, Wilmington
OhioMidwest Eye Center, Cincinnati
Velocity Clinical Research, Mt. Auburn, Cincinnati
TexasPlanIt Research, LLC, Houston
PlanIt Research, LLC (Monitoring Room), Houston
VIP Trials, San Antonio
VirginiaYork Clinical Research, LLC, Norfolk

Conditions

From ClinicalTrials.gov, data retrieved Oct 1, 2026. Each study sets its own eligibility; the study team decides who can join.