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2 Information about avapritinib

Marketing authorisation indication

2.1 On 24 September 2020 the European Medicines Agency (EMA) granted conditional marketing authorisation for avapritinib for the treatment of unresectable or metastatic gastrointestinal stromal tumours (GIST) that have the platelet-derived growth factor receptor alpha (PDGFRA) D842V mutation.

Dosage in the marketing authorisation

2.2 The dosage schedule will be available in the summary of product characteristics [add hyperlink when available].

Price

2.3 Avapritinib costs £26,666.67 for 30 tablets (100 mg, 200 mg or 300 mg; excluding VAT; company submission).

The company has a commercial arrangement, which would have applied if the technology had been recommended.