Ireland
--:--IST
Recruiting Observational

Ravulizumab Treatment Outcomes in Patients With Generalized Myasthenia Gravis

NCT06909253 · tracked via the Priya Life Science Poland tracker
Phase
Observational
Started
2025-05-15
Last updated
2026-09-16

Condition(s) studied

Myasthenia Gravis, Generalized

Investigational drug(s) / intervention(s)

Ravulizumab →

Ravulizumab: Ravulizumab, concentrate for solution for infusion

Study summary

The Polish multicentre observational (non-interventional) study aiming to collect data on the management and clinical outcomes of patients with gMG that received ravulizumab.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult (aged ≥18 years) patients with gMG, naive to complement inhibitors, receiving ravulizumab treatment in the frames of NDP in Poland. * Patients willing to participate in the study and signed Informed Consent Form (ICF). * Vaccination against N. meningitidis Exclusion Criteria: * Those who plan to participate in gMG clinical trial on/after the date of first ravulizumab infusion through NDP. * Cognitive incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.

Primary outcome measure(s)

  • Change from baseline in Myasthenia Gravis-Activities of Daily Living (MG-ADL) total score — at 6 month

Trial sites (11)

FacilityCityRegionStatus
Research Site Bydgoszcz Poland Recruiting
Research Site Gdansk Poland Recruiting
Research Site Katowice Poland Recruiting
Research Site Krakow Poland Recruiting
Research Site L DZ Poland Recruiting
Research Site Lublin Poland Recruiting
Research Site Poznan Poland Recruiting
Research Site Szczecin Poland Recruiting
Research Site Szczecin Poland Withdrawn
Research Site Warsaw Poland Recruiting
Research Site Wroclaw Poland Recruiting
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 NCT06909253 on ClinicalTrials.gov ↗ ← All trials in Poland