To appraise the clinical and cost effectiveness of tofacitinib within its marketing authorisation for treating active psoriatic arthritis in adults whose disease has not responded adequately to previous disease-modifying anti-rheumatic drug (DMARD) therapy, or for whom DMARDs are not tolerated or contraindicated.
 
Status Proposed
Process STA
ID number 1220

Project Team

Project lead Michelle Adhemar

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Timeline

Key events during the development of the guidance:

Date Update
19 September 2017 - 17 October 2017 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators

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