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Study details
Enrolling now

A Study of MET233 in Combination With MET097

Metsera, a wholly owned subsidiary of Pfizer
NCT IDNCT06924320ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

132

Study length

about 11 months

Ages

18–75

Locations

1 site in CA

What this study is about

Researchers are testing a treatment combination (MET233 and MET097) for people with obesity or overweight, possibly including those with diabetes. The trial will examine the safety and how well the medication works in the body.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take MET233
  • 2.Take MET233 and MET097
  • 3.Take Placebo

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Part A: Occurrence of treatment-emergent adverse events (TEAEs), Part B: Occurrence of treatment-emergent adverse events (TEAEs), Part C: Occurrence of treatment-emergent adverse events (TEAEs)

Secondary: Part A: Area under the concentration versus time curve (AUC), Part A: Maximum observed concentration (Cmax), Part A: Percent change from baseline in body weight, Part A: Time to maximum observed concentration (Tmax), Part B: Area under the concentration versus time curve (AUC), Part B: Maximum observed concentration (Cmax), Part B: Percent change from baseline in body weight, Part B: Time to maximum observed concentration (Tmax)

Body systems

Endocrinology