Suggested Remit: To appraise the clinical and cost effectiveness of nintedanib with pemetrexed and cisplatin followed by nintedanib monotherapy within its marketing authorisation for untreated unresectable malignant pleural mesothelioma.

The company have informed us that they are no longer seeking regulatory approval in this indication. Therefore the appraisal is suspended.

Status:
Discontinued
Technology type:
Medicine
Decision:
Prioritised
Process:
TA
ID number:
1424

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Timeline

Key events during the development of the guidance:

Date Update
25 August 2022 Discontinued. The company have informed us that they are no longer seeking regulatory approval in this indication. Therefore the appraisal is suspended.
20 July 2020 Note added to the project documents
09 March 2020 Note added to the project documents
09 March 2020 Suspended. Topic is suspended
11 June 2018 - 09 July 2018 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators
24 April 2018 In progress. DHSC Referral Received

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