💬In plain words
What the trial is, and whether it could suit you
This is an open-label, multicenter, interventional phase 3b study in participants with AChR+ gMG and severe exacerbation that require hospitalization. Patients will receive subcutaneous zilucoplan injections daily for 12 weeks. Participation in the study will last for approximately 18 weeks.
Sign in to get the eligibility rules as simple questions to take to your doctor.
📋 Eligibility rules (as published)
Inclusion Criteria:
* Patient determined to have severe MG exacerbation (e.g. bulbar and/or respiratory symptoms requiring hospitalization, neck extension weakness)
* MGFA class II - IVb
* Male or female aged ≥18
* MG-ADL ≥6 in non-ocular domains
* Serology - AChR antibody positive (or historically available data)
* If female of child-bearing potential (i.e., not surgically sterile or post-menopausal defined as age \> 51 years without menses for ≥ 2 years), negative serum pregnancy test at screening
* Women of child-bearing potential or men with sexual partners of childbearing potential must be willing to use an acceptable method of birth control for the duration of the study and for 40 days after the last dose of study drug therapy. Acceptable methods of birth control include abstinence, oral contraceptives, the contraceptive patch, intra-uterine device, the contraceptive ring, and or barrier contraception such as condoms with spermicide.
* Completed or updated meningococcal vaccination or initiated meningococcal vaccination with appropriate antibiotic prophylaxis according to current USPI and ACIP guidelines
Exclusion Criteria:
* History of meningococcal disease
* Participants requiring intubation prior to study start.
* Recent significant infections which could have caused exacerbation e.g. sepsis and wound infections
* Pregnancy or lactating
* Recent surgery (\<4 weeks). Minor procedures/surgeries allowed at the discretion of the site principal investigator
* Current use or known failure of C5 inhibitors in the previous 3 months
* Initiation of plasma exchange or IVIG in the past 4 weeks
* Participation in concurrent clinical trial with a therapeutic medication
* Rituximab use in the previous 9 months
* Any clinically significant condition or illness, which, in the opinion of the PI, would pose a risk to the subject or might confound the study
University of South Florida/Tampa General Hospital
Tampa, United States
University of Kansas Medical Center
Kansas City, United States
The Ohio State University
Columbus, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.