RecruitingPhase 2NCT07570758

A Phase 2A Clinical Trial to Assess the Safety and Tolerability of ERX1000 in Men and Women for the Treatment of Obesity.

A Phase 2A, Randomized, Double-Blind, Placebo-Controlled, Clinical Study to Assess Efficacy, Safety and Tolerability of Orally Administered ERX1000 in Subjects With Obesity


Sponsor

ERX Pharmaceuticals

Enrollment

80 participants

Start Date

May 28, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The primary objective is to assess the safety and tolerability of oral dose ERX1000 in obese subjects.


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called ERX1000 and Placebo for people with obesity, overweight. The study is currently recruiting participants at 3 locations. People eligible for this study include aged 18 Years to 60 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGERX1000

2mg tablet administered orally twice weekly.

OTHERPlacebo

2mg Placebo tablet identical in appearance to 2mg ERX1000 tablet


Locations(3)

Monroe Biomedical Research

Louisville, Kentucky, United States

Monroe Biomedical Research

Monroe, North Carolina, United States

Monroe Biomedical Research

North Charleston, South Carolina, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07570758


Related Trials