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DOVATO is indicated for the treatment of Human Immunodeficiency Virus type 1 (HIV-1) infection in adults and adolescents above 12 years of age weighing at least 40 kg, with no known or suspected resistance to the integrase inhibitor class, or lamivudine DOVATO is indicated as a complete regimen to treat HIV-1 infection in adults and adolescents 12 years of age and older and weighing at least 25 kg with no antiretroviral (ARV) treatment history or to replace the current ARV regimen in those who are virologically suppressed (HIV-1 RNA <50 copies mL) on a stable ARV regimen with no history of What countries does “ Europe ” mean for Dovato patent coverage? “ Europe ” in searches can mean EU member states (and sometimes the UK or EEA countries) Coverage can differ by jurisdiction because: - European patents may be validated country-by-country after grant, and - local enforcement depends on each national validation and court process View Dovato EMA approval details, including marketing authorisation, regulatory status, and therapeutic information Dovato (dolutegravir and lamivudine) information for Healthcare Professionals registered in Ireland DOVATO Film-coated tablet Ref [10718] Active ingredients: Dolutegravir Lamivudine Lamivudine and Dolutegravir Source: European Medicines Agency ( EU ) Revision Year: 2023 Publisher: ViiV Healthcare BV, Van Asch van Wijckstraat 55H, 3811 LP Amersfoort, Netherlands Jul 3, 2019 · The new regimen, dubbed Dovato , is approved in adults and adolescents above 12 years of age with HIV-1, and is based on a combination of dolutegravir and lamivudine given as a single pill once
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