Patient's signs and symptoms should not be better explained by another disease process.
Prednisone dose of at least 10 mg/day (or the equivalent in alternate days) and the subject must be on a stable dose of prednisone for 30 days prior to the screening visit.
You may not be if
A history of chronic degenerative, psychiatric, or neurologic disorder other than MG that can produce weakness or fatigue.
Other major chronic or debilitating illnesses within six months prior to study entry.
Female patients who are premenopausal and are: (a) pregnant on the basis of a serum pregnancy test, (b) breast-feeding, or (c) not using an effective method of double barrier (1 hormonal plus 1 barrier method or 2 simultaneous barrier methods) birth control (birth control pills, male condom, female condom, intrauterine device, Norplant, tubal ligation, or other sterilization procedures).
Altered levels of consciousness, dementia, or abnormal mental status.
Evidence of thymoma on chest CT or MRI. Such a finding could require immediate thymectomy and would preclude entry into the study.
Thymectomy in the previous three months.
Patients who have been medicated with azathioprine, cyclosporine, cyclophosphamide, mycophenolate mofetil, IVIg, or other immunosuppressive drugs within the last 60 days.
Chest X-ray with evidence of tumor, infection, or interstitial lung disease.
Clinical history of chronic or recurrent infections.
Daily use of non-steroidal anti-inflammatory drugs (NSAIDs).
History of renal or hepatic insufficiency or liver enzymes greater than the upper limit of normal.
History of bone marrow hypoplasia, leucopenia, thrombocytopenia, significant anemia, clinical or laboratory evidence of immunodeficiency syndromes.
Forced Vital Capacity (FVC) \<50% of predicted.
MG Grade 1 (ocular only) or 5 (crisis, requiring ventilator).
Prior use of methotrexate for any condition.
Clareo Health | Efficacy of Methotrexate in Myasthenia Gravis
