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Clinical Trials in the USA / NCT07656727
Active, not recruiting Phase 2

A Phase 2 Study to Evaluate the Pharmacodynamics, Safety and Tolerability of BGE-102 in Participants With Obesity and Cardiovascular Risk Factors

NCT07656727 · tracked via the Priya Life Science USA tracker
Sponsor
BioAge Labs, Inc.
Phase
Phase 2
Started
2026-06-11
Last updated
2026-09-10

Condition(s) studied

Obesity and Cardiovascular Risk

Investigational drug(s) / intervention(s)

Oral BGE-102 →Oral Placebo Matching BGE-102

Oral BGE-102: Capsules

Oral Placebo Matching BGE-102: Capsules

Study summary

The purpose of this study is to learn about the effects of BGE-102 on blood biomarkers including hsCRP, which is a lab value used to measure inflammation. BGE-102 decreases inflammation which may improve obesity and cardiovascular health. Participants will receive either BGE-102 or placebo. This study will be checking safety and tolerability of BGE-102.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: * Obese Male and Female adults with BMI 32-42 kg/m² * Elevated blood test for hsCRP consistent with chronic systemic inflammation * At least one cardiovascular risk factor or metabolic syndrome feature * Stable background therapies and willing to maintain stable diet/exercise habits during the study Key Exclusion Criteria: * Type 1 diabetes, * Uncontrolled Type 2 diabetes, * Uncontrolled hypertension and /or hyperlipidemia * Recent weight change of 5% or more, * Use of weight-loss medications/programs * Clinically relevant medical condition(s) that put the participant at risk or will make implementation of the protocol or interpretation of the study difficult. * Clinically significant ECG abnormalities or arrhythmias * Use of prohibited medications (including GLP-1 therapies, immunosuppressants, chronic anti-inflammatory drugs, or moderate or strong CYP3A4 modulators) * Contraindications to MRI * Clinically significant gastric emptying abnormality (e.g., severe gastroparesis or gastric outlet obstruction) or take drugs that directly affect GI motility, have undergone prior surgical treatment for obesity (e.g., gastric bypass \[bariatric\] surgery or restrictive bariatric surgery), or have an endoscopic and/or device-based therapy for obesity * Women who are pregnant or nursing

Primary outcome measure(s)

Trial sites (17)

FacilityCityRegionStatus
Site 108 Chandler Arizona
Site 115 Peoria Arizona
Site 110 Tucson Arizona
Site 100 Rogers Arkansas
Site 109 Maitland Florida
Site 102 Miami Florida
Site 104 Port Orange Florida
Site 103 Lexington Kentucky
Site 106 Rockville Maryland
Site 113 Kansas City Missouri
Site 116 Las Vegas Nevada
Site 111 Hartsdale New York
Site 112 Austin Texas
Site 114 Dallas Texas
Site 101 San Antonio Texas
Site 117 Sugar Land Texas
Site 105 San Juan Puerto Rico

More BioAge Labs, Inc. trials in the USA

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 NCT07656727 on ClinicalTrials.gov ↗ ← All trials in the USA