ClinicalTrials.Veeva

Menu

The Impact of Myasthenia Gravis in the Real World

V

Vitaccess

Status

Completed

Conditions

Myasthenia Gravis

Study type

Observational

Funder types

Industry

Identifiers

NCT04176211
5105-08-2019

Details and patient eligibility

About

An international, non-interventional, prospective, community recruited, longitudinal, lifestyle study which aims to collect Real-World Evidence (RWE) from people living with myasthenia gravis (MG) in order to map the disease's natural history, its burden on patients and their families, its treatment, as well as its medical, social and pharmacoeconomic impact.

Full description

Data was collected from people with MG using the MyRealWorld™ RWE platform , developed by the healthcare digital research company, Vitaccess. Participants downloaded a 'bring your own device' (BYOD) study app, MyRealWorld™ MG, onto their smartphones, which they used to enter data and complete surveys about their MG.

Enrollment

2,847 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults (aged 18 years and over) with any stage and any subtype of myasthenia gravis disease
  • Resident in Belgium, Canada, France, Germany, Italy, Japan, Spain, the UK, the USA, or Denmark

Exclusion criteria

  • No specific exclusion criteria

Trial contacts and locations

1

Loading...

Central trial contact

Mark JW Larkin, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems