RecruitingPhase 1Phase 2NCT07815678

First-in-human Study of the Safety, Tolerability, Pharmacokinetics, and Food Effect of ACCG-2671

A Randomized, Double-blind, Placebo-controlled, First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Food-effect of ACCG-2671


Sponsor

Aconcagua Bio, Inc. a wholly owned subsidiary of Structure Therapeutics

Enrollment

164 participants

Start Date

Dec 29, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This first-in-human study will evaluate the safety, tolerability, and pharmacokinetics of single and multiple ascending oral doses of ACCG-2671. It will also evaluate the effect of food on the pharmacokinetics, safety, and tolerability of a single dose. Parts 1 and 2 will enroll healthy participants, and Part 3 will enroll otherwise healthy participants with obesity.


Eligibility

Min Age: 25 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called ACCG-2671 and a drug called Placebo for people with obesity. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 25 Years to 75 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.

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Interventions

DRUGACCG-2671

Administered orally

DRUGPlacebo

Administered orally


Locations(6)

Research Site

Cypress, California, United States

Research Site

Lake Forest, California, United States

Research Site

Decatur, Georgia, United States

Research Site

Dilworth, Minnesota, United States

Research Site

Springfield, Missouri, United States

Research Site

Webster, Texas, United States

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NCT07815678


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