NCT06717425CompletedPhase 2
A Study to Learn About the Study Medicine Called PF-07976016 in Adults With Obesity
A PHASE 2A, RANDOMIZED, DOUBLE-BLIND, SPONSOR-OPEN, PLACEBO-CONTROLLED, PARALLEL GROUP, DOSE-RANGING STUDY OF PF-07976016 TO ASSESS SAFETY AND EFFICACY IN ADULT PARTICIPANTS WITH OBESITY
Source: ClinicalTrials.gov · Last updated 6 Feb 2026
Brief summary (registry, in English)
The purpose of this clinical trial is to learn about the safety and effects of the study medicine (called PF-07976016) for the potential treatment of obesity. The study will compare the experiences of participants taking the study medicine (PF-07976016) to those of participants who take placebo (a lookalike substance that contains no active study medicine). The aim is to measure the body's response to the study medicine, including any changes in participants' body weight and how well they tolerate the study medicine.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 263 (actual)
- First submitted
- 2 Dec 2024
- Start date
- 9 Dec 2024
- Primary completion date
- 23 Oct 2025
- Lead sponsor
- Pfizer
- Diseases
- Obesity
- NCT number
- NCT06717425
- EU CT number
- 2024-513679-42-00
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 263
- From 9 Dec 2024 to the primary completion date, 23 Oct 2025
- 42 sites in 4 countries
- 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
- Use of any prohibited prior or concomitant medication(s)
Lab values
- Any medical or psychiatric condition or laboratory abnormality, or recent serious illness or hospitalization, that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study including diagnosis of type 2 diabetes mellitus, type 1 or secondary forms of diabetes.
- Presence of specified abnormalities on diagnostic assessments including clinical laboratory tests at Visit 1.
Who the study is looking for
- Male or non-pregnant, non-breastfeeding female, 18 to 74 years of age at Visit 1
- Body Mass Index ≥30.0 kg/m2 at Visit 1, with stable body weight, defined as \<5 kg change in the 12 weeks before Visit 1
- Eligible and willing to receive required background medicine
- Willing and able to comply with all study procedures
Age in the registry: 18 years to 74 years · Sex: All · Does not accept healthy volunteers
Sites (42)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dawson Clinical Research Inc. Coordinator of this site? Confirm its status | Guelph | Canada | Unknown status |
| The Wharton Medical Clinic Clinical Trials Inc Coordinator of this site? Confirm its status | Hamilton | Canada | Unknown status |
| Milestone Research Inc. Coordinator of this site? Confirm its status | London | Canada | Unknown status |
| Ocean West Research Clinic Coordinator of this site? Confirm its status | Surrey | Canada | Unknown status |
| Canadian Phase Onward Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| DRC Kft. Coordinator of this site? Confirm its status | Balatonfüred | Hungary | Completed |
| University of Debrecen Coordinator of this site? Confirm its status | Debrecen | Hungary | Completed |
| Belinus Bt. Coordinator of this site? Confirm its status | Debrecen | Hungary | Completed |
| Studium Egeszseghaz Kft Coordinator of this site? Confirm its status | Kalocsa | Hungary | Completed |
| Borbanya Praxis Egeszsegugyi Kft Coordinator of this site? Confirm its status | Nyíregyháza | Hungary | Completed |
| Centrum Badan Klinicznych PI-House sp. z o.o. Coordinator of this site? Confirm its status | Gdansk | Poland | Completed |
| Pratia S.A. Coordinator of this site? Confirm its status | Gdynia | Poland | Completed |
| EKAMED sp. z o.o. Coordinator of this site? Confirm its status | Lublin | Poland | Completed |
| Medicome Sp. z o.o. Coordinator of this site? Confirm its status | Oswiecim | Poland | Completed |
| Centrum Zdrowia Metabolicznego Paweł Bogdański Coordinator of this site? Confirm its status | Poznan | Poland | Completed |
| Anaheim Clinical Trials, LLC Coordinator of this site? Confirm its status | Anaheim | United States | Unknown status |
| University of Colorado Anschutz Medical Campus Coordinator of this site? Confirm its status | Aurora | United States | Unknown status |
| Clinical & Translational Research Center Coordinator of this site? Confirm its status | Aurora | United States | Unknown status |
| Elligo Clinical Research Center Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| Texas Diabetes & Endocrinology, P.A. Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| Pennington Biomedical Research Center Coordinator of this site? Confirm its status | Baton Rouge | United States | Unknown status |
| Capital Area Research, LLC Coordinator of this site? Confirm its status | Camp Hill | United States | Unknown status |
| StudyMetrix Research Coordinator of this site? Confirm its status | City of Saint Peters | United States | Unknown status |
| UT Southwestern Medical Center Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| Velocity Clinical Research, Dallas Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| East-West Medical Research Institute Coordinator of this site? Confirm its status | Honolulu | United States | Unknown status |
| Westside Center for Clinical Research Coordinator of this site? Confirm its status | Jacksonville | United States | Unknown status |
| L-MARC Research Center Coordinator of this site? Confirm its status | Louisville | United States | Unknown status |
| New Horizon Research Center Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| AMR Clinical Coordinator of this site? Confirm its status | Norman | United States | Unknown status |
| Cornerstone Nutrition and Diabetes Coordinator of this site? Confirm its status | Norman | United States | Unknown status |
| Renstar Medical Research Coordinator of this site? Confirm its status | Ocala | United States | Unknown status |
| Rochester Clinical Research, LLC Coordinator of this site? Confirm its status | Rochester | United States | Unknown status |
| St. Johns Center for Clinical Research Coordinator of this site? Confirm its status | Saint Augustine | United States | Unknown status |
| Artemis Institute for Clinical Research Coordinator of this site? Confirm its status | San Diego | United States | Unknown status |
| Consano Clinical Research, LLC Coordinator of this site? Confirm its status | Shavano Park | United States | Unknown status |
| Chrysalis Clinical Research Coordinator of this site? Confirm its status | St. George | United States | Unknown status |
| Southwest Internal Medicine, PC Coordinator of this site? Confirm its status | St. George | United States | Unknown status |
| Cotton O'Neil Diabetes & Endocrinology Coordinator of this site? Confirm its status | Topeka | United States | Unknown status |
| Rophe Adult and Pediatric Medicine/SKYCRNG Coordinator of this site? Confirm its status | Union City | United States | Unknown status |
| Accellacare - Wilmington Coordinator of this site? Confirm its status | Wilmington | United States | Unknown status |
| Selma Medical Associates Coordinator of this site? Confirm its status | Winchester | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.