{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T15:05:19Z","timestamp":1791212719378,"version":"4.1.0"},"reference-count":29,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2018,10,4]],"date-time":"2018-10-04T00:00:00Z","timestamp":1538611200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Aliment Pharmacol Ther"],"published-print":{"date-parts":[[2018,11]]},"abstract":"<jats:title>Summary<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>In 2017, the hepatitis C treatment regimens sofosbuvir\/velpatasvir\/voxilaprevir (<jats:styled-content style=\"fixed-case\">SOF<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VEL<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VOX<\/jats:styled-content>) and glecaprevir\/pibrentasvir (G\/P) received approval from the U.S. Food and Drug Administration. Although both <jats:styled-content style=\"fixed-case\">SOF<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VEL<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VOX<\/jats:styled-content> (<jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>5B polymerase inhibitor\/<jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>5A inhibitor\/<jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>3\/4A protease inhibitor) and G\/P (<jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>3\/4A protease inhibitor\/<jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>5A inhibitor) are pangenotypic regimens, they are indicated for distinct subsets of patients with hepatitis C.<\/jats:p><\/jats:sec><jats:sec><jats:title>Aim<\/jats:title><jats:p>To compare and contrast available safety and efficacy data for <jats:styled-content style=\"fixed-case\">SOF<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VEL<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VOX<\/jats:styled-content> and G\/P and outline their clinical utility.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>For each of the regimens, this review outlines the indications, safety information, and the major clinical studies in which <jats:styled-content style=\"fixed-case\">SOF<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VEL<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VOX<\/jats:styled-content> and G\/P were evaluated.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">SOF<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VEL<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VOX<\/jats:styled-content> is positioned as a salvage regimen for patients previously treated with <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>5A inhibitors and for genotype 1a\u2010 and 3\u2010infected patients who had failed other sofosbuvir\u2010containing regimens. G\/P is the first pangenotypic regimen with an 8\u2010week duration for treatment\u2010na\u00efve, non\u2010cirrhotic patients, and it is indicated for patients with any genotype who have advanced kidney disease, including those on dialysis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The addition of <jats:styled-content style=\"fixed-case\">SOF<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VEL<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VOX<\/jats:styled-content> and G\/P to existing hepatitis C treatment options will expand the number of patients who are eligible for and responsive to treatment, thus increasing the possibility of eliminating hepatitis C as a public health issue.<\/jats:p><\/jats:sec>","DOI":"10.1111\/apt.14977","type":"journal-article","created":{"date-parts":[[2018,10,6]],"date-time":"2018-10-06T04:00:25Z","timestamp":1538798425000},"page":"914-923","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":16,"title":["Review article: novel antivirals for hepatitis C\u2014sofosbuvir\/velpatasvir\/voxilaprevir, glecaprevir\/pibrentasvir"],"prefix":"10.1111","volume":"48","author":[{"given":"Brian L.","family":"Pearlman","sequence":"first","affiliation":[{"name":"Center for Hepatitis C Wellstar Atlanta Medical Center Atlanta Georgia"},{"name":"The Medical College of Georgia Augusta Georgia"},{"name":"Emory School of Medicine Atlanta Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew E.","family":"Hinds","sequence":"additional","affiliation":[{"name":"Center for Hepatitis C Wellstar Atlanta Medical Center Atlanta Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2018,10,4]]},"reference":[{"key":"e_1_2_8_2_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-0031-1297928"},{"key":"e_1_2_8_3_1","doi-asserted-by":"publisher","DOI":"10.1001\/jama.2014.7085"},{"key":"e_1_2_8_4_1","doi-asserted-by":"publisher","DOI":"10.2147\/IJGM.S127689"},{"key":"e_1_2_8_5_1","doi-asserted-by":"publisher","DOI":"10.1080\/17474124.2017.1351295"},{"key":"e_1_2_8_6_1","unstructured":"Gilead Sciences.VOSEVI: Highlights of Prescribing Information.http:\/\/www.gilead.com\/~\/media\/files\/pdfs\/medicines\/liver-disease\/vosevi\/vosevi_pi.pdf. 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