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Completed Phase 3 Interventional Results available

An Open-label Study to Investigate the Clinical Efficacy of Different Dosing Regimens of Efgartigimod IV in Patients With Generalized Myasthenia Gravis

ClinicalTrials.gov ID: NCT04980495

Public ClinicalTrials.gov record NCT04980495. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:52 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3b, Randomized, Open-label, Parallel-Group Study to Evaluate Different Dosing Regimens of Intravenous Efgartigimod to Maximize and Maintain Clinical Benefit in Patients With Generalized Myasthenia Gravis

Study identification

NCT ID
NCT04980495
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
argenx
Industry
Enrollment
69 participants

Conditions and interventions

Interventions

  • Efgartigimod IV Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 15, 2021
Primary completion
Aug 23, 2023
Completion
Oct 5, 2025
Last update posted
May 26, 2026

2021 – 2025

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Investigator Site 10 - US0010007 Carlsbad California 92011
Investigator Site 7 - US0010001 Orange California 92868
Investigator Site 9 - 0010006 Boca Raton Florida 33487
Investigator Site 15 - US0010014 Coral Springs Florida 33067
Investigator Site 16 - US0010009 Augusta Georgia 30910
Investigator Site 8 - US0010003 Chicago Illinois 60611
Investigator Site 6 - US0010008 Meadows Illinois 60008
Investigator Site 12 - US0010004 Kansas City Kansas 66160
Investigator Site 13 - US0010013 Portland Oregon 97239
Investigator Site 17 - US0010012 Philadelphia Pennsylvania 19104
Investigator Site 11 - US0010011 Austin Texas 78756
Investigator Site 14 - US0010010 Richmond Virginia 23219

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04980495, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 26, 2026 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04980495 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →