Glecaprevir is a direct acting antiviral agent and Hepatitis C virus (HCV) NS3/4A protease inhibitor that targets the the viral RNA replication. In combination with Pibrentasvir, glecaprevir is a useful therapy for patients who experienced therapeutic failure from other NS3/4A protease inhibitors. It demonstrates a high genetic barrier against resistance mutations of the virus. In cell cultures, the emergence of amino acid substitutions at NS3 resistance-associated positions A156 or D/Q168 in HCV genotype 1a, 2a or 3a replicons led to reduced susceptibility to glecaprevir . The combinations of amino acid substitutions at NS3 position Y65H and D/Q168 also results in greater reductions in glecaprevir susceptibility, and NS3 Q80R in genotype 3a patients also leads to glecaprevir resistance .
Glecaprevir is available as an oral combination therapy with Pibrentasvir under the brand name Mavyret. This fixed-dose combination therapy was FDA-approved in August 2017 to treat adults with chronic hepatitis C virus (HCV) genotypes 1-6 without cirrhosis (liver disease) or with mild cirrhosis, including patients with moderate to severe kidney disease and those who are on dialysis . Mavyret is also indicated for HCV genotype 1-infected patients who have been previously treated with regimens either containing an NS5A inhibitor or an NS3/4A protease inhibitor, but not both . Hepatitis C viral infection often leads to decreased liver function and subsequent liver failure, causing a significantly negative impact on the patients' quality of life. The ultimate goal of the combination treatment is to achieve sustained virologic response (SVR) and cure the patients from the infection. In clinical trials, this combination therapy achieved SVR12 rate, or undetectable Hepatitis C for twelve or more weeks after the end of treatment, of ≥93% across genotypes 1a, 2a, 3a, 4, 5 and 6 .
Indicated for the treatment of adult patients with chronic hepatitis C virus (HCV) genotype 1, 2, 3, 4, 5 or 6 infection without cirrhosis or with compensated cirrhosis (Child-Pugh
A). MAVYRET is also indicated for the treatment of adult patients with HCV genotype 1 infection, who previously have been treated with a regimen containing an HCV NS5A inhibitor
or an NS3/4A protease inhibitor (PI), but not both .
National Taiwan University Hospital, Yun-Lin Branch, Douliu, Taiwan
National Taiwan University Hospital, Taipei, Taiwan
University Health Network Toronto General Hospital, Toronto, Ontario, Canada
Jullums Lismore Aboriginal Medical Service, Lismore, New South Wales, Australia
Walhallow Aboriginal Corporation, Quirindi, New South Wales, Australia
Pangula Mannamurna Aboriginal Corporation, Mount Gambier, South Australia, Australia
New York University School of Medicine, New York, New York, United States
NUAA NSP, Sydney, New South Wales, Australia
Guangdong General Hospital /ID# 156827, Guangzhou, Guangdong, China
The First Hosp of Jilin Univ /ID# 156825, Changchun, Jilin, China
West China Hospital /ID# 156835, Chengdu, Sichuan, China
The Third Affiliated Hospital Of Sun Yat-Sen University /ID# 156900, Guangzhou, Guangdong, China
Xiangya Hospital Central South University /ID# 156901, Changsha, Hunan, China
Jiangsu Province People's Hospital /ID# 156861, Nanjing, Jiangsu, China
Hospital de Clinicas de Porto Alegre /ID# 163167, Porto Alegre, Rio Grande Do Sul, Brazil
Hospital Ernesto Dornelles /ID# 163171, Porto Alegre, Rio Grande Do Sul, Brazil
Hospital de Clinicas de Porto Alegre /ID# 163166, Porto Alegre, Rio Grande Do Sul, Brazil
Univ Maryland School Medicine /ID# 161157, Baltimore, Maryland, United States
Digestive Disease Associates - Baltimore /ID# 161260, Baltimore, Maryland, United States
University of Vermont Medical Center /ID# 161263, Burlington, Vermont, United States
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