Skip to main content
OpenTrials
Completed

NCT Number: NCT06867718

Study of Once-Daily Oral RGT001-075 Compared With Placebo in Adults With Obesity or Are Overweight With Weight-Related Health Conditions

This is a phase 2, 36-week randomized, double-blind, placebo-controlled, parallel arm study that will evaluate the safety, tolerability, weight loss efficacy, pharmacodynamic effects, and pharmacokinetics of RGT001-075 in adults who are obese (BMI ≥30 kg/m²) or who are overweight (BMI ≥27 kg/m²) with at least one weight-related comorbidity. RGT001-075 or matching placebo will be administered once daily.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Alliance for Multispecialty Research, LLC, Mobile, Alabama, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female, age 18-75 years (inclusive) at the time of signing informed consent.
  • Hemoglobin A1c (HbA1c) <6.5% at screening.
  • BMI ≥30 kg/m².
  • BMI ≥27 kg/m² and <30 kg/m² with at least 1 weight-related comorbidity:
  • hypertension
  • dyslipidemia
  • cardiovascular (CV) disease
  • obstructive sleep apnea
  • Have a stable body weight (< 5% change) for the 3 months prior to randomization.

Exclusion criteria

(Obesity Related):

  • Have obesity induced by other endocrine disorders (for example, Cushing's syndrome) or diagnosed monogenetic or syndromic forms of obesity (for example, Melanocortin 4 Receptor deficiency or Prader-Willi Syndrome).
  • Have a prior or planned surgical treatment for obesity.
  • Have or plan to have endoscopic and/or device-based therapy for obesity or have had device removal within the last 6 months before screening such as mucosal ablation, gastric artery embolization, intragastric balloon, duodenal-jejunal endoluminal liner.
  • Have been treated with prescribed or OTC drugs or alternative remedies that promote weight loss within the last 3 months before screening.

Exclusion criteria

(Medical Conditions)

  • Diabetes.
  • Have a history of acute or chronic pancreatitis.
  • Have current symptomatic gallbladder disease or biliary disease.
  • Have known liver disease other than MASLD.
  • Have a known self or family history (first-degree relative) of multiple endocrine neoplasia type 2A or type 2B, thyroid C-cell hyperplasia, or medullary thyroid carcinoma (MTC).
  • Have a serum calcitonin ≥20 pg/mL.
  • Have an eGFR <30 mL/min/1.73 m², as determined by the central laboratory at screening.
  • Have a history of Major Depressive Disorder (MDD) or other severe psychiatric disorders (e.g., schizophrenia or bipolar disorder) within the last 2 years.
  • Have had any exposure to GLP-1 analogs, or other related compounds within the prior 3 months or any prior history of clinically significant side effects from GLP-1 receptor agonist (GLP-1 RA) or other related compounds containing GLP-1.

Treatment and study plan

RGT001-075

Drug

RGT001-075 is a small molecule GLP-1 agonist

placebo comparator

Drug

Placebo comparator

Primary outcomes

  1. Percent change from baseline in body weight at Week 36

    Time frame: Baseline and 36 weeks

    Least Squares (LS) mean using mixed model repeated measures (MMRM)

Secondary outcomes

  1. Percent change from baseline in body weight at Week 26

    Time frame: Baseline and 26 weeks

    Least Squares (LS) mean using mixed model repeated measures (MMRM)

  2. Incidence of treatment emergent adverse events (TEAEs), TESAEs, TEAESIs overall

    Time frame: Baseline through week 36

    To evaluate the safety and tolerability of RGT001-075 for weight loss in adults who are obese, or overweight with at least one weight-related comorbidity

  3. Ambulatory Blood Pressure Monitoring (ABPM)

    Time frame: Baseline, 26 weeks

    The ABPM device will be attached to the nondominant arm, and participants will be instructed to wear the monitor for a 24- to 27-hour period.

  4. AUC0-last

    Time frame: week 15

    Area under the serum concentration curve from time-zero to the last quantifiable concentration of RGT001-075

  5. AUC0-inf

    Time frame: week 15

    Area under curve from time zero to time infinite

  6. Cmax

    Time frame: week15

    Maximum concentration of RT001-075

  7. Tmax

    Time frame: week 15

    Time to achieve maximum concentration of RT001-075

  8. t1/2

    Time frame: week 15

    Terminal half-life of RGT001-075

Sponsors and collaborators

Lead sponsor

Regor Pharmaceuticals Inc.

Industry

Registry information

Official study title

A Phase 2 Study of Once-Daily RGT001-075 Compared With Placebo in Participants Who Have Obesity or Are Overweight With Weight-Related Comorbidities (COMO-1)

Acronym: COMO-1

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Mar 10, 2025
Registry last updated
May 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.