The GiACTA study evaluated the safety and efficacy of ACTEMRA for the treatment of GCA in 251 patients with new onset or relapsing GCA (cranial GCA and large vessel vasculitis) who were enrolled and assigned to one of four treatment arms. The study consisted of a 52 week blinded period (Part 1), followed by a 104 week open label extension (Part 2). Relationships between ACTEMRA concentrations to safety and efficacy endpoints were assessed.
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