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NCT07142707 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MBX 4291 in Adult Participants With Obesity

A Phase 1 study of Obesity, sponsored by MBX Biosciences.

Recruiting
Registry status
Phase 1
Development phase
64
Enrollment target
1
Study location

NCT07142707: Recruiting Phase 1 study of Obesity, sponsored by MBX Biosciences.

NCT07142707 is a Phase 1 study of Obesity that is actively recruiting participants, run by MBX Biosciences. The registered enrollment target is 64 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07142707, a Phase 1 study of Obesity, is actively recruiting participants, sponsored by MBX Biosciences.

RECRUITING
Registry status
Phase 1
Development phase
64 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the safety and tolerability of single and multiple subcutaneous (SC) doses of MBX 4291 in adults with obesity.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG MBX 4291

Study Locations (1)

Tennessee

  • MBX Biosciences Investigational Site - Knoxville

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2025-09-03
Est. Completion 2026-05-30
Phase Phase 1
MBX Biosciences

7 total trials

What NCT07142707 shows while recruiting

NCT07142707 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (92% lower).

The record links to 1 condition, with Obesity appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07142707 reports a single indexed study location in Tennessee.

Frequently Asked Questions

What is clinical trial NCT07142707 about?

NCT07142707 is a clinical study titled "A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MBX 4291 in Adult Participants With Obesity". The purpose of this study is to evaluate the safety and tolerability of single and multiple subcutaneous (SC) doses of MBX 4291 in adults with obesity.

What is the current status of trial NCT07142707?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2025-09-03. Estimated completion is 2026-05-30.

What conditions does trial NCT07142707 study?

This clinical trial studies the following conditions: Obesity.

What interventions are being tested in trial NCT07142707?

The interventions under investigation include: Placebo (DRUG), MBX 4291 (DRUG).

Who is sponsoring clinical trial NCT07142707?

This trial is sponsored by MBX Biosciences, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07142707 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Obesity

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07142707's enrollment target sits among peer trials

64 623rd of 1053 higher than 428 of 1,053 other Obesity trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Obesity trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07142707, the US trial registry maintained by the National Library of Medicine. NCT07142707 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.