RecruitingPhase 3NCT07570316

A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves' Disease

A Phase 3, Randomized, Double-Masked, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves' Disease Inadequately Controlled With Antithyroid Drugs


Sponsor

argenx

Enrollment

230 participants

Start Date

Jun 10, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The main purpose of this study is to look at how efgartigimod affects thyroid function in adults with Graves' Disease (GD). The study will also check whether efgartigimod is safe and well tolerated. It will look at how efgartigimod is distributed and eliminated in the body, how it changes antibody levels, and how the immune system responds to it. The study consists of a part A double-blinded treatment period, a part B treatment/observation period and a part C open-label treatment/observation period. During the part A and part B treatment periods, participants will receive efgartigimod PH20 SC via Prefilled Syringe (PFS) or placebo. During the part C open-label treatment period, participants will receive efgartigimod PH20 SC PFS. Participation in the different parts of the study will depend on the participant's response to treatment. The total study duration for participants ranges from 63 to 135 weeks, depending on the response to treatment. More information can be found here: https://clinicaltrials.argenx.com/vitalithy


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a biological treatment called Efgartigimod PH20 SC and Placebo PH20 SC for people with graves disease. The study is currently recruiting participants at 18 locations.

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

BIOLOGICALEfgartigimod PH20 SC

Subcutaneous injection of Efgartigimod PH20 Via Prefilled Syringe (PFS)

OTHERPlacebo PH20 SC

Subcutaneous injection of placebo PH20 via Prefilled Syringe (PFS)


Locations(18)

Diabetes Associates Medical Group

Orange, California, United States

Havana Research Institute LLC.

Pasadena, California, United States

Northeast Florida Endocrine & Diabetes Associates (NEFEDA) - Orange Park Location

Fleming Island, Florida, United States

The Center for Diabetes and Endocrine Care

Fort Lauderdale, Florida, United States

Ilumina Medical Research LLC

Kissimmee, Florida, United States

Johnson County Clin-Trials, Inc.

Lenexa, Kansas, United States

Metro Detroit Endocrinology Center

Dearborn, Michigan, United States

Profound Research

Farmington Hills, Michigan, United States

Endocrine Associates of West Village PC

New York, New York, United States

Research Institute of Dallas

Dallas, Texas, United States

Juno Research

Houston, Texas, United States

Tekton Research Irving

Irving, Texas, United States

Biopharma Informatic, LLC

McAllen, Texas, United States

Tekton Research - McKinney

McKinney, Texas, United States

Southern Endocrinology Associates PA

Mesquite, Texas, United States

Consano Clinical Research

Shavano Park, Texas, United States

New Hospitals

Tbilisi, Georgia

LLC Todua Clinic

Tbilisi, Georgia

View Full Details on ClinicalTrials.gov

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NCT07570316


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