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elvitegravir (Vitekta®)

 

Following non-submission

AWMSG advice

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.

 Statement of Advice (SOA): elvitegravir (Vitekta) 1061 (PDF, 187Kb)

Medicine details

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

Company Gilead Sciences Ltd
BNF chapter Infections
Assessment type Non-submission
Status Not endorsed (Statement of Advice)
Date of issue 07/05/2014
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