Simponi — CareFirst (Caremark)
Immunotherapy-related inflammatory arthritis
Initial criteria
- Member is using the requested medication for immunotherapy-related inflammatory arthritis
 - Member achieves or maintains a positive clinical response with the requested medication as evidenced by low disease activity or improvement in signs and symptoms of the condition
 - Member has had a documented negative tuberculosis (TB) test (tuberculosis skin test [TST] or interferon-release assay [IGRA]) within 12 months of initiating therapy for persons naïve to biologic drugs or targeted synthetic drugs associated with increased risk of TB
 - If TB screening is positive, further testing confirms no active disease (e.g., chest x-ray)
 - Do not administer the requested medication to members with active TB infection
 - If there is latent TB disease, TB treatment must be started before initiation of the requested medication
 - Member cannot use the requested medication concomitantly with any other biologic drug or targeted synthetic drug for the same indication
 
Reauthorization criteria
- Member continues to achieve or maintain a positive clinical response with the requested medication as evidenced by low disease activity or improvement in signs and symptoms of the condition
 
Approval duration
12 months