RAND. CLINICAL TRIAL OF HIGH DOSE IMMUNOBLATIVE THERA
$183,570N01FY2000ARNIH
Johns Hopkins University, Baltimore MD
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Abstract
This is a phase II, open label study that compares the efficacy of intravenous monthly iv. cyclophosphamide (NIH protocol) to high dose intravenous cyclophosphamide (immunoablative protocol) in the treatment of moderate to severe SLE. Patients will be followed for 24 months after therapy.
View original record on NIH RePORTER →