RecruitingPhase 1NCT07487376

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of a Single Dose of IBIO-600 in Overweight or Obese Adults

A Phase I, First-in-Human, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of IBIO-600 in Overweight or Obese Adult Participants (IBIO-600-CT001).


Sponsor

iBio, Inc.

Enrollment

32 participants

Start Date

May 24, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to learn which dose of study drug IBIO-600 has the right balance of safety, tolerability and impact on body composition in overweight and obese adult participants.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called IBIO-600 and a drug called Placebo for people with overweight/obesity. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 65 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

DRUGIBIO-600

IBIO-600 Subcutaneous injection

DRUGPlacebo

Matching placebo; subcutaneous injection


Locations(1)

Veritus Research

Bayswater, Victoria, Australia

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NCT07487376


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