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Clinical Trials in the USA / NCT06064461
Recruiting Observational

Vitaccess Real MG Registry

NCT06064461 · tracked via the Priya Life Science USA tracker
Sponsor
Vitaccess Ltd
Phase
Observational
Started
2024-07-31
Last updated
2025-07-29

Condition(s) studied

Myasthenia Gravis

Study summary

Vitaccess Real MG (VRMG) is a patient registry designed to capture longitudinal observational data on myasthenia gravis (MG), its treatment, and impact on symptoms, daily activities, and quality of life (QoL). The duration of the registry is 10 years from launch, and approximately 600 patients will be recruited in the US and Europe with no defined upper limit. The registry will link relevant patient- and healthcare professional (HCP)-reported data with clinical data from medical records.

Patients will be recruited at clinical sites in all participating countries. In the US only, patients can additionally be recruited via community neurologists or direct-to-patient recruitment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Adult (age ≥18 years) with a clinically-confirmed diagnosis of myasthenia gravis (MG). * Resident in one of the scope countries. * Access to a smartphone/tablet/computer/laptop * Willing and able to provide informed consent in their local language to take part in the study. Exclusion Criteria: * Participation in a clinical trial at the time of study enrolment.

Primary outcome measure(s)

Trial sites (8)

FacilityCityRegionStatus
UCI Health Orange California Recruiting
HSHS St. Elizabeth's Hospital O'Fallon Illinois Recruiting
UK HealthCare - University of Kentucky Lexington Kentucky Recruiting
Neurology Associates of South Jersey Lumberton New Jersey Recruiting
Medical University South Carolina Charleston South Carolina Recruiting
University of Texas Health Science Center at Houston Houston Texas Recruiting
Vitaccess Ltd London London Recruiting
University Hospitals Birmingham Birmingham United Kingdom Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06064461 on ClinicalTrials.gov ↗ ← All trials in the USA