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Durham, NC, February 5, 2024 – ViiV Healthcare, the global specialist HIV company majority owned by GSK, with Pfizer and Shionogi as shareholders, today announced Dovato (dolutegravir lamivudine) is now available in a blister pack in the U S Dovato is approved as a complete regimen to treat HIV-1 infection in adults with no antiretroviral (ARV) treatment history or to replace the current DOVATO is approved in Canada, US, Europe, Japan, Australia, and other countries worldwide Please consult the Product Monograph at --- viivhealthcare ca for complete safety information The six discrete real world cohorts have been identified, mainly located in Europe , and provide data for treatment-naïve patients, treatment experienced patients, patients with various comorbidities, and patients with a history of virologic failure Potential overlap between cohorts cannot be ruled out Treatment-Naïve Patients viivhealthcare com viiv-healthcare-presents-data-from-second-dovatous gsk com us-fda-approves-viiv-healthcare-s-dovato-dolutegravirlamivudin --- ema europa eu en documents dovato-epar-product-information_en pdfviivhealthcare com en-us media-center news dovato-blister-packDoes Dovato interact with cladribine? Should Dovato be discontinued? Is dovatoor a 2-drug regimen? finance yahoo com viiv-healthcare-announces-positive-data-120100140 html 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 EU 1 19 1370 004 Dovato 50 mg 300 mg Film-coated tablet Oral use blister (PVC PCTFE) 90 (3 x 30) tablets (multipack) Title: Dovato , INN-dolutegravir, lamivudine Administration of a single Dovato tablet with a high fat meal increased dolutegravir AUC(0-∞) and Cmax by 33% and 21%, respectively, and decreased the lamivudine Cmax by 30% compared to fasted conditions The lamivudine AUC(0-∞) was not affected by a high fat meal These changes are not clinically significant Overview Dovato is a medicine for treating infection with human immunodeficiency virus type 1 (HIV-1), a virus that causes acquired immune deficiency syndrome (AIDS) It is used to treat adults and adolescents over 12 years old who weigh at least 40 kg This medicine contains the active substances dolutegravir and lamivudine and is used to --- europeanpharmaceuticalreview com three-year-dovato-study-shows-non-in --- gsk com us-fda-approves-viiv-healthcare-s-dovato-dolutegravirlamivudi What is Dovato used for? Dovato is a once-daily, single-pill, 2DR that combines the integrase strand transfer inhibitor (INSTI) dolutegravir (Tivicay, 50mg) with the nucleoside reverse transcriptase inhibitor (NRTI) lamivudine (Epivir, 300mg) How to store Dovato? Jul 11, 2019 · ViiV Healthcare has announced that the European Commission has granted marketing authorisation for Dovato (dolutegravir lamivudine) for the treatment of HIV-1 infection in adults and adolescents above 12 years of age weighing at least 40kg, with no known or suspected resistance to the integrase inhibitor class, or lamivudine Issued: London, UK ViiV Healthcare today announced that the US Food and Drug Administration (FDA) approved Dovato, a complete, once-daily, single-tablet regimen of dolutegravir (DTG) 50 mg and lamivudine (3TC) 300 mg for the treatment of HIV-1 infection in adults with no antiretroviral (ARV) treatment history and with no known resistance to either DTG or 3TC Dovato (dolutegravir 50 mg lamivudine 300 mg tablets) is authorised in the EU for the treatment of 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 approved in the US, Europe, Japan and other countries worldwide Trademarks are owned by or licensed to the ViiV Healthcare group of companies Important Safety Information for Dovato (50mg dolutegravir 300mg lamivudine) Tablets Dovato is a medicine for treating infection with human immunodeficiency virus type 1 (HIV-1), a virus that causes acquired immune deficiency syndrome (AIDS) It is used to treat adults and adolescents over 12 years old who weigh at least 40 kg DOVATO is authorised for the treatment of HIV infection (see SmPC for the full indication) It contains dolutegravir and lamivudine as the active substances and it is given as a tablet by mouth Further information about the evaluation of DOVATO’s benefits can be found in DOVATO’s EPAR, including in its plain-language summary, available on It was approved for use in the United States in April 2019, [4] [6] [7] and in the European Union in July 2019, [5] and again with revisions in June 2022 [5] [8] The most common side effects are headache, diarrhea, nausea, and difficulty sleeping [5] The most common serious side effects are allergic reactions, including rash and severe liver --- ema europa eu en dovato-epar-risk-management-plan-summary_en pdfHow do you take Dovato? Issued: London ViiV Healthcare today announced that the US Food and Drug Administration (FDA) approved Dovato, a complete, once-daily, single-tablet regimen of dolutegravir (DTG) 50 mg and lamivudine (3TC) 300 mg for the treatment of HIV-1 infection in adults with no antiretroviral (ARV) treatment history and with no known resistance to either DTG or 3TC --- ema europa eu en medicines human EPAR dovato In the EU, dolutegravir lamivudine 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 kilograms (88 lb), with no known or suspected resistance to the integrase inhibitor class, or lamivudine [5] en wikipedia org wiki Dolutegravir lamivudinePeople also ask
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