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NCT07022977 · ClinicalTrials.gov registry record · Phase 1
A Study of MET233 in Individuals With Obesity or Overweight
A Phase 1 study of Obesity and Overweight, sponsored by Metsera, a wholly owned subsidiary of Pfizer.
- Active
- Registry status
- Phase 1
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT07022977 is a Phase 1 study of Obesity and Overweight that is active but no longer recruiting, run by Metsera, a wholly owned subsidiary of Pfizer. The registered enrollment target is 120 participants, below the 461-participant average among 27 other Obesity and Overweight trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07022977, a Phase 1 study of Obesity and Overweight, is active but no longer recruiting, sponsored by Metsera, a wholly owned subsidiary of Pfizer.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 1
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of once-weekly subcutaneous injections of MET233 in otherwise healthy adults with overweight or obesity. The trial will be conducted in three parts. Part A consists of single ascending dose (SAD) cohorts of MET233 or placebo. Part B consists of multiple ascending dose (MAD) cohorts, with participants treated with five once-weekly doses of MET233 or placebo. In Part C, participants will receive once-weekly doses of MET233 or placebo for 12 weeks, followed by a single higher, potential monthly dose.
Conditions Studied
Interventions
- BIOLOGICAL Placebo
- BIOLOGICAL MET233
Study Locations (1)
California
- MET233 Research Site 001 - Cypress
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2024-11-20 |
| Est. Completion | 2026-04-15 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07022977
The ClinicalTrials.gov registry entry for NCT07022977 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 461-participant average among 27 other Obesity and Overweight trials with a reported enrollment target (74% lower). The listed sponsor is Metsera, a wholly owned subsidiary of Pfizer, which has 7 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Obesity and Overweight appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT07022977 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT07022977 about?
NCT07022977 is a clinical study titled "A Study of MET233 in Individuals With Obesity or Overweight". The goal of this clinical trial is to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of once-weekly subcutaneous injections of MET233 in otherwise healthy adults with overweight or obesity. The trial will be conducted in three parts. Part A consists of single ascending dose...
What is the current status of trial NCT07022977?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 120 participants. The study started on 2024-11-20. Estimated completion is 2026-04-15.
What conditions does trial NCT07022977 study?
This clinical trial studies the following conditions: Obesity and Overweight.
What interventions are being tested in trial NCT07022977?
The interventions under investigation include: Placebo (BIOLOGICAL), MET233 (BIOLOGICAL).
Who is sponsoring clinical trial NCT07022977?
This trial is sponsored by Metsera, a wholly owned subsidiary of Pfizer, which has 7 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07022977 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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