Written question asked by Lord Beamish (Labour) on Monday, 5 September 2022, in the House of Commons. It was due for an answer on Thursday, 8 September 2022 (named day). A holding answer was provided on Thursday, 8 September 2022. A substantive answer was provided by Robert Jenrick (Conservative) on Tuesday, 20 September 2022 on behalf of the Department of Health and Social Care.
Tixagevimab/cilgavimab
- Question
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To ask the Secretary of State for Health and Social Care, when he expects NICE's review of Evusheld to be concluded.
- Answer
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On 10 August 2022, the Department referred tixagevimab and cilgavimab (Evusheld) to the National Institute for Health and Care Excellence (NICE) to evaluate its clinical and cost effectiveness for preventing COVID-19. Between 29 July and 12 August, NICE consulted with stakeholders on the suggested remit, draft scope and list of consultees and commentators.
NICE has commenced this evaluation and currently expects to publish draft guidance in April 2023, with final guidance to follow in May 2023. In discussion with AstraZeneca, NICE is expediting the appraisal process by bringing forward the deadline for the manufacturer’s evidence submission.
Secondary information
- Type
- Written question
- Reference
- 47379
- Session
- 2022-23
- Subjects
- Testing Tixagevimab/cilgavimab
- Link
- View this Written question on www.parliament.uk
Librarians' tools
- Timestamp
- 2024-05-24 10:03:43 +0100
- URI
- http://data.parliament.uk/writtenparliamentaryquestion/commons/2022-23/47379
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- http://indexing.parliament.uk/Content/Edit/1?uri=http://data.parliament.uk/writtenparliamentaryquestion/commons/2022-23/47379
- In Solr
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