BGE-102 for Obesity and Cardiovascular Risk Factors

This study is testing a new oral medication called BGE-102 in adults who have obesity and risk factors for heart disease. The main goal is to see how BGE-102 affects inflammation in the body, measured by a blood test called hsCRP. Researchers believe that BGE-102 might help improve obesity and heart health by reducing inflammation. You would receive either BGE-102 or a placebo (an inactive capsule that looks like the study drug). The study will also check how safe BGE-102 is and if people can tolerate it well. To join, you need to be an adult with a BMI between 32-42 kg/m², have high hsCRP levels, and at least one heart disease risk factor or feature of metabolic syndrome. The study is currently recruiting participants.

Study design
This is a Phase 2 interventional study with 160 planned participants. Participants will be randomly assigned to receive one of three doses of BGE-102 or a placebo.
What's involved
The study lasts about 20 weeks, with 12 weeks of treatment. You would have visits every 2 weeks for the first month of treatment, then every 4 weeks until week 16.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for 4 weeks after the 12-week treatment period.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07656727

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

Recruiting
PHASE2Ages 18+InterventionalTreatment
BioAge Labs, Inc.
~160 participants
Updated 2026-06-18 on ClinicalTrials.gov
What's tested:Oral BGE-102Oral Placebo Matching BGE-102

At a glance

Recruiting sites
12 of 13 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percent change in hsCRP (Dose A)
Measured over Week 12
+2 more outcomes measured
Obesity and Cardiovascular Risk
13 sites across 8 states
Arizona3
Florida3
Texas2
Arkansas1
Kentucky1
Maryland1
Missouri1
Puerto Rico1

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Eligibility criteria

Inclusion

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

Exclusion

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
  • Percent change in hsCRP (Dose A)Week 12

    Percent change in hsCRP of the BGE-102 Dose A daily compared to Placebo

  • Percent change in hsCRP (Dose B)Week 12

    Percent change in hsCRP of the BGE-102 Dose B daily compared to Placebo

  • Percent change in hsCRP (Dose C)Week 12

    Percent change in hsCRP of the BGE-102 Dose C daily compared to Placebo