Yuflyma — CareFirst (Caremark)
Immune checkpoint inhibitor-related inflammatory arthritis
Initial criteria
- Member age ≥ 2 years (for uveitis)
 - Requested medication is used for an indication outlined in the coverage criteria section
 - Member has a documented negative tuberculosis (TB) test within 12 months of initiating therapy for persons naïve to biologic or targeted synthetic drugs associated with increased TB risk
 - If TB screening is positive, further testing confirms no active disease (e.g., chest x-ray)
 - Do not administer requested medication to members with active TB infection
 - If latent TB disease is present, TB treatment must be started before initiation of requested medication
 - Member is not using the requested medication concomitantly with any other biologic drug or targeted synthetic drug for the same indication
 - For rheumatoid arthritis: member must initiate treatment with every other week dosing
 
Reauthorization criteria
- Uveitis: Member continues to achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms, meeting any of the following:
 - • Reduced frequency of disease flares compared to baseline
 - • Stability or improvement in anterior chamber (AC) cell grade compared to baseline
 - • Stability or improvement in vitreous haze (VH) grade compared to baseline
 - • Stability or improvement in visual acuity compared to baseline
 - • Reduction in glucocorticoid requirements from baseline
 - • No new active inflammatory chorioretinal and/or inflammatory retinal vascular lesions relative to baseline
 - Immune checkpoint inhibitor-related inflammatory arthritis: Member achieves or maintains a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms
 - All other covered indications: Member achieves or maintains a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms
 
Approval duration
12 months