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

Part of paid clinical trials in Roseville, California.

Sponsor
Pfizer
Study ID
NCT07595549
Phase
PHASE3
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • PF-08653944 — DRUG
    By Subcutaneous Injection
  • Placebo — OTHER
    By 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

Start date
Jun 10, 2026
Status verified
Jun 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 1
    Participants will receive PF-08653944 by Subcutaneous Injection.
  • Experimental: Treatment Arm 2
    Participants will receive PF-08653944 by Subcutaneous Injection.
  • Experimental: Treatment Arm 3
    Participants will receive PF-08653944 by Subcutaneous Injection.
  • Experimental: Treatment Arm 4
    Participants will receive PF-08653944 by Subcutaneous Injection.
  • Placebo Comparator: Placebo
    Participants will receive matching placebo by Subcutaneous Injection.

Primary Outcome Measure

Percent change from baseline in body weight [ Time Frame: Baseline, Week 72 ]

Central Contacts

Locations (9)

FacilityCityStateZIPSite coordinators
ClearVue Eye CareRosevilleCalifornia95661-
Clinical Trials ResearchSacramentoCalifornia95821-
Nature Coast Clinical ResearchCrystal RiverFlorida34429-
West Coast Eye InstituteLecantoFlorida34461-
MediSphere Medical Research Center, LLCEvansvilleIndiana47714-
Albuquerque Clinical Trials, Inc.AlbuquerqueNew Mexico87102-
Rochester Clinical Research, LLCRochesterNew York14609-
Midwest Eye CenterCincinnatiOhio45202-
Velocity Clinical Research, Mt. AuburnCincinnatiOhio45219-

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