Suggested remit - To appraise the clinical and cost effectiveness of rituximab within its marketing authorisation for maintenance treatment of anti-neutrophil cytoplasmic antibody-associated vasculitis.
 
Status Awaiting development
Decision None selected
Process STA pre-2018
ID number 1320

Project Team

Project lead Emily Richards

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Timeline

Key events during the development of the guidance:

Date Update
20 March 2018 - 19 April 2018 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators

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