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:
- Adults aged 18 or older who have been diagnosed with generalised Myasthenia Gravis (a muscle weakness condition), have never previously been treated with a type of drug called a complement inhibitor, and are currently receiving a medicine called ravulizumab through a special national drug programme in Poland.
- People who are willing to take part and have signed a consent form agreeing to participate.
- People who have been vaccinated against a specific type of bacterial infection called meningococcal disease (caused by N. meningitidis).
Who may not be able to join:
- People who are planning to take part in another clinical trial for generalised Myasthenia Gravis at the same time as, or after, their first ravulizumab treatment through the national drug programme.
- People who have difficulty understanding or communicating due to cognitive (thinking or memory) difficulties, unwillingness to cooperate, or language barriers that would prevent them from fully understanding the study.
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: 1-877-240-9479
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
Change from baseline in Myasthenia Gravis-Activities of Daily Living (MG-ADL) total score
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.