Myasthenia Gravis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are 18 years of age or older
- You have been diagnosed with generalized Myasthenia Gravis (a muscle weakness condition), confirmed by medical records, a physical examination, and a specific blood test showing certain antibodies (AChR-Abs)
- You have received more than one round of a blood-filtering treatment (called plasma exchange/PLEX) or an intravenous antibody infusion treatment (IVIg) as part of your care
- Your muscle weakness condition has been classified as a severe level (class IV or V) by medical standards at the time of your ICU admission
- You have already been treated with at least one standard medication used for Myasthenia Gravis
- You are receiving a specific medication called Ravulizumab during your ICU stay, after plasma exchange or IVIg treatment, and this has been approved by specialists from a French rare disease medical network (FILNEMUS)
- You are able to understand and sign a consent form agreeing to take part — if muscle weakness prevents you from signing, a trusted witness may sign on your behalf
- You are willing and able to attend scheduled appointments and follow the study plan
- You are covered by a European social security/health insurance system
- You agree to take steps to prevent a serious bacterial infection called meningococcal disease, through vaccination and/or preventive antibiotics as recommended locally
- You have no medical reason preventing you from taking anti-C5 treatment (the type of drug used in this trial)
- You have no medical reason preventing you from taking antibiotics
Who may not be able to join:
- You have an active infection, or another condition causing muscle weakness, a known immune deficiency (IgA deficiency), active kidney or liver disease, significant heart disease, or a blood-thickening disorder
- You currently have any form of cancer
- You have antibodies in your blood other than the specific AChR antibodies (having anti-titin antibodies alongside AChR antibodies is permitted — confirm with trial site)
- You have a tumour of the thymus gland (called a thymoma)
- You have another health condition that the study doctor believes could interfere with the trial
- You have a positive pregnancy test (women of childbearing age will be tested)
- You have a mental health condition, dementia, or other condition that, in the study doctor's opinion, may affect your ability to understand or follow the study
- You have received a live vaccine within the past 6 weeks
- You do not wish to take part in the study
- You are legally protected or under guardianship in a way that prevents participation in a clinical study under French law
- You have a known allergy or sensitivity to the study drug or any of its ingredients
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 0492035757
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Short-term change in clinical outcomes; Short-term change in clinical outcomes; Short-term change in clinical outcomes
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.