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Clinical Trials in the UK / NCT07284875
Recruiting Phase 3

Efficacy and Safety of Ribupatide in Participants Living With Obesity or Overweight With Weight-Related Comorbidities Who Do Not Have Diabetes

NCT07284875 · tracked via the Priya Life Science UK tracker
Sponsor
Kailera
Phase
Phase 3
Started
2025-12-18
Last updated
2026-09-03

Condition(s) studied

ObesityOverweight

Investigational drug(s) / intervention(s)

RibupatidePlacebo

Ribupatide: SC Injection

Placebo: SC Injection

Study summary

The primary objective of the study is to determine the effects of ribupatide (KAI-9531) subcutaneous (SC) injection once weekly compared to placebo on percent change in body weight.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * BMI ≥30 kg/m\^2 or BMI ≥27 kg/m\^2 and previously diagnosed with at least 1 of the following: 1. hypertension, 2. dyslipidemia, 3. obstructive sleep apnea, or 4. cardiovascular (CV) disease. * History of being unresponsive to at least 1 self-reported effort to lose weight with diet and/or exercise in the last 6 months. Exclusion Criteria: * Current diagnosis or history of diabetes mellitus. * Started medications within 3 months prior to Screening that may cause significant weight change, including, but not limited to: tricyclic antidepressants, atypical antipsychotics, mood stabilizers, or phentermine. * Unstable weight defined as self-reported change in body weight exceeding 5% within 3 months prior to Screening. * Family or personal history of multiple endocrine neoplasia Type 2 or medullary thyroid cancer. * Uncontrolled hypertension or unstable cardiovascular disease. * History of chronic or acute pancreatitis. * Known clinically significant gastric-emptying abnormality or chronic treatment with medications that directly affect gastrointestinal motility. * History of suicide attempt. * History of significant active or unstable Major Depressive Disorder (MDD) or other severe psychiatric disorder. * Received treatment with semaglutide, tirzepatide, GLP-1 receptor agonist, GLP-1/glucose-dependent insulinotropic polypeptide (GIP), or glucagon receptor agonist within 3 months prior to Screening. Note: Additional inclusion/exclusion criteria may apply, per protocol.

Primary outcome measure(s)

Trial sites (104)

FacilityCityRegionStatus
Kailera Clinical Site Anniston Alabama Recruiting
Kailera Clinical Site Birmingham Alabama Recruiting
Kailera Clinical Site Cullman Alabama Recruiting
Kailera Clinical Site Sun City Arizona Recruiting
Kailera Clinical Site Escondido California Recruiting
Kailera Clinical Site Toluca Lake California Recruiting
Kailera Clinical Site Aurora Colorado Recruiting
Kailera Clinical Site Bridgeport Connecticut Recruiting
Kailera Clinical Site Jupiter Florida Recruiting
Kailera Clinical Site Lilburn Georgia Recruiting
Kailera Clinical Site Springfield Illinois Recruiting
Kailera Clinical Site Columbia Maryland Recruiting
Kailera Clinical Site Las Vegas Nevada Recruiting
Kailera Clinical Site Rochester New York Recruiting
Kailera Clinical Site Morehead City North Carolina Recruiting
Kailera Clinical Site Chickasha Oklahoma Recruiting
Kailera Clinical Site Mauldin South Carolina Recruiting
Kailera Clinical Site Chattanooga Tennessee Recruiting
Kailera Clinical Site Amarillo Texas Recruiting
Kailera Clinical Site Bellaire Texas Recruiting
Kailera Clinical Site DeSoto Texas Recruiting
Kailera Clinical Site Tomball Texas Recruiting
Kailera Clinical Site Salt Lake City Utah Recruiting
Kailera Clinical Site Danville Virginia Recruiting
Kailera Clinical Site La Plata Buenos Aires Recruiting
Kailera Clinical Site San Nicolás de los Arroyos Buenos Aires Recruiting
Kailera Clinical Site Buenos Aires Buenos Aires F.D. Recruiting
Kailera Clinical Site Buenos Aires Buenos Aires F.D. Recruiting
Kailera Clinical Site Buenos Aires Buenos Aires F.D. Recruiting
Kailera Clinical Site Godoy Cruz Mendoza Province Recruiting
Kailera Clinical Site Rosario Santa Fe Province Recruiting
Kailera Clinical Site CABA Argentina Recruiting
Kailera Clinical Site Córdoba Argentina Recruiting
Kailera Clinical Site Charlestown New South Wales Recruiting
Kailera Clinical Site Sydney New South Wales Recruiting
Kailera Clinical Site Sydney New South Wales Recruiting
Kailera Clinical Site Sydney New South Wales Recruiting
Kailera Clinical Site Wollongong New South Wales Recruiting
Kailera Clinical Site Sippy Downs Queensland Recruiting
Kailera Clinical Site Norwood South Australia Recruiting

+ 64 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07284875 on ClinicalTrials.gov ↗ ← All trials in the UK