Vitaccess Real MG Registry
Eligible age
18+ yrs
Accepts
All genders
Locations
6 states
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
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.
Sponsor: Vitaccess Ltd
You may qualify if…
- ✓ 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.
You may not qualify if…
- ✕ Participation in a clinical trial at the time of study enrolment.
Where it's recruiting
Orange
O'Fallon
Lexington
Lumberton
Charleston
Houston
Source: ClinicalTrials.gov · NCT06064461 · last updated 2025-07-29