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Recruiting Phase 1Phase 2 Interventional

Study of Aritinercept in Patients With Generalized Myasthenia Gravis

ClinicalTrials.gov ID: NCT07596901

Public ClinicalTrials.gov record NCT07596901. 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 Sep 20, 2026, 8:21 AM 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 Double-Blind, Randomized, Placebo-Controlled Study to Investigate the Safety and Efficacy of Aritinercept, a Dual BAFF/APRIL Inhibitor, in Patients With Generalized Myasthenia Gravis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This clinical study will enroll patients with generalized myasthenia gravis (gMG). The goal of this clinical study is to assess the safety, tolerability, effectiveness, pharmacokinetics (how the body processes the drug) and pharmacodynamics (how the drug affects the body) of aritinercept.

Study identification

NCT ID
NCT07596901
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Aurinia Pharmaceuticals Inc.
Industry
Enrollment
81 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 85 Years
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
Apr 21, 2026
Primary completion
Mar 1, 2029
Completion
Mar 1, 2029
Last update posted
Aug 2, 2026

2026 – 2029

United States locations

U.S. sites
11
U.S. states
5
U.S. cities
10
Facility City State ZIP Site status
Aurinia Investigational Site Pasadena California 91106 Recruiting
Aurinia Investigational Site Altamonte Springs Florida 32714 Recruiting
Aurinia Investigational Site Boca Raton Florida 33487 Recruiting
Aurinia Investigational Site Homestead Florida 33033 Recruiting
Aurinia Investigational Site Miami Florida 33155 Recruiting
Aurinia Investigational Site Miami Florida 33173 Recruiting
Aurinia Investigational Site Chicago Illinois 60616 Recruiting
Aurinia Investigational Site O'Fallon Illinois 62269 Recruiting
Aurinia Investigational Site Dearborn Michigan 48126 Recruiting
Aurinia Investigational Site Flint Michigan 48507 Recruiting
Aurinia Investigational Site Houston Texas 77027 Recruiting

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07596901, 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 Aug 2, 2026 · Synced Sep 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07596901 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →