Ontology highlight
ABSTRACT: Background
Familial Mediterranean fever (FMF) is an inherited disorder caused by a number of mutations of the Mediterranean fever (MEFV) gene, coding a protein named pyrin that acts as a major regulatory component of the inflammasome. The first-line drug for FMF treatment is colchicine, but 10% of patients with FMF do not respond well to colchicine. Although the efficacy of tocilizumab (TCZ), which is a recombinant, humanized, antihuman interleukin 6 (IL-6) receptor monoclonal antibody, has been reported to prevent FMF attacks, the effects of TCZ on individuals with colchicine-resistant or colchicine-intolerant FMF have not been evaluated in a randomized clinical trial.Methods/design
In this phase III, investigator-initiated, multicenter, double-blind, randomized, parallel-
SUBMITTER: Koga T
PROVIDER: S-EPMC6311086 | biostudies-literature | 2018 Dec
REPOSITORIES: biostudies-literature