Following non-submission
AWMSG advice |
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Status: Not endorsed (Statement of Advice) | ||
In the absence of a submission from the holder of the marketing authorisation, elvitegravir (Vitekta®), co-administered with ritonavir-boosted protease inhibitor and with other antiretroviral agents, cannot be endorsed for use within NHS Wales for the treatment of human immunodeficiency virus-1 (HIV-1) infection in adults who are infected with HIV-1 without known mutations associated with resistance to elvitegravir. This product is currently not marketed in the UK. |
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Medicine details |
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Medicine name | elvitegravir (Vitekta®) | |
Formulation | 85 mg and 150 mg film-coated tablet | |
Reference number | 1061 | |
Indication | Co-administered with ritonavir-boosted protease inhibitor and with other antiretroviral agents, for the treatment of human immunodeficiency virus-1 (HIV-1) infection in adults who are infected with HIV-1 without known mutations associated with resistance to elvitegravir |
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Company | Gilead Sciences Ltd | |
BNF chapter | Infections | |
Assessment type | Non-submission | |
Status | Not endorsed (Statement of Advice) | |
Date of issue | 07/05/2014 |