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Response to certolizumab pegol in the RAPID-PsA trial was comparable to other TNF inhibitors in PsA, with 58% of the certolizumab pegol 200 mg every-2-weeks group and 51.9% of the certolizumab pegol 400 mg every-4-weeks group achieving an ACR20 at 12 weeks compared with 24.3% in the placebo arm (Figure 7-16)

For details on these policies, see section IV.B.5.c

After consideration of public comments, we are finalizing without modification our proposal at 512.705 to define specialty type as the medical specialty determined by the specialty code indicated on the plurality of a clinician's Medicare Part B claims