A Study to Learn About the Study Medicine Called Berobenatide (PF-08653944) in People With Overweight or Obesity
Part of paid clinical trials in Canoga Park, California.
- Sponsor
- Pfizer
- Study ID
- NCT07595549
- Phase
- PHASE3
- Status
- Recruiting
Conditions
- Obesity
- Overweight
- Overweight and/or Obesity
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- PF-08653944 — DRUGBy Subcutaneous Injection
- Placebo — OTHERBy Subcutaneous Injection
Study Details
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.
Key Dates
- First listed
- May 19, 2026
- Start date
- Jun 10, 2026
- Status verified
- Sep 2026
- Primary completion
- May 4, 2028
- Completion
- Jun 21, 2028
Study Design
- Enrollment
- 954 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment Arm 1Participants will receive PF-08653944 by Subcutaneous Injection.
- Experimental: Treatment Arm 2Participants will receive PF-08653944 by Subcutaneous Injection.
- Experimental: Treatment Arm 3Participants will receive PF-08653944 by Subcutaneous Injection.
- Experimental: Treatment Arm 4Participants will receive PF-08653944 by Subcutaneous Injection.
- Placebo Comparator: PlaceboParticipants will receive matching placebo by Subcutaneous Injection.
Primary Outcome Measure
Percent change from baseline in body weight [ Time Frame: Baseline, Week 72 ]
Central Contacts
- Pfizer CT.gov Call Center1-800-718-1021
Locations (34)
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