MedPath

Glecaprevir

Generic Name
Glecaprevir
Brand Names
Maviret, Mavyret
Drug Type
Small Molecule
Chemical Formula
C38H46F4N6O9S
CAS Number
1365970-03-1
Unique Ingredient Identifier
K6BUU8J72P
Background

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 .

Indication

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 .

Associated Conditions
Chronic Hepatitis C - Genotype 3, Chronic Hepatitis C Genotype 1, Chronic Hepatitis C Virus (HCV) Infection, Chronic hepatitis C genotype 2, Chronic hepatitis C genotype 5, Genotype 4 Chronic Hepatitis C, Genotype 6 chronic hepatitis C infection

Pharmacokinetics and Safety of ABT-493 and ABT-530 in Subjects With Normal and Impaired Renal Function

Phase 1
Completed
Conditions
Renal Impairment
Interventions
First Posted Date
2015-05-13
Last Posted Date
2016-02-22
Lead Sponsor
AbbVie
Target Recruit Count
46
Registration Number
NCT02442258
Locations
🇺🇸

Site Reference ID/Investigator# 132890, Miami, Florida, United States

🇳🇿

Site Reference ID/Investigator# 137332, Grafton, Auckland, New Zealand

🇺🇸

Site Reference ID/Investigator# 132889, Orlando, Florida, United States

A Study to Assess Resistance and Durability of Response to ABT-493 and/or ABT-530

Phase 2
Completed
Conditions
Hepatitis C
Interventions
First Posted Date
2015-05-12
Last Posted Date
2020-09-21
Lead Sponsor
AbbVie
Target Recruit Count
384
Registration Number
NCT02441283
Locations
🇨🇦

Toronto Liver Centre /ID# 155401, Toronto, Ontario, Canada

🇺🇸

Digestive Health Specialists of the Southeast /ID# 136725, Dothan, Alabama, United States

🇺🇸

Southern California Res. Ctr. /ID# 141799, Coronado, California, United States

and more 39 locations

Pharmacokinetics and Safety of ABT-493 and/or ABT-530 in Subjects With Normal and Impaired Hepatic Function

Phase 1
Completed
Conditions
Hepatic Impairment
Interventions
First Posted Date
2014-11-21
Last Posted Date
2015-10-21
Lead Sponsor
AbbVie
Target Recruit Count
24
Registration Number
NCT02296905
Locations
🇳🇿

Site Reference ID/Investigator# 130590, Grafton, New Zealand

🇺🇸

Site Reference ID/Investigator# 130588, San Antonio, Texas, United States

🇺🇸

Site Reference ID/Investigator# 130589, Miami, Florida, United States

and more 1 locations

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-administration of ABT-493 and ABT-530 With and Without Ribavirin in Subjects With HCV Genotype 1, 4, 5, and 6 Infection

Phase 2
Completed
Conditions
HCV
Hepatitis C Virus
Chronic Hepatitis C
Interventions
First Posted Date
2014-09-17
Last Posted Date
2021-07-13
Lead Sponsor
AbbVie
Target Recruit Count
174
Registration Number
NCT02243280

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administration of ABT-493 and ABT-530 With and Without RBV in Subjects With Chronic Hepatitis C Virus (HCV) Genotypes 2, 3, 4, 5 or 6 Infection

Phase 2
Completed
Conditions
Hepatitis C Virus
Chronic Hepatitis C
Interventions
First Posted Date
2014-09-17
Last Posted Date
2021-07-30
Lead Sponsor
AbbVie
Target Recruit Count
694
Registration Number
NCT02243293

A Study to Evaluate the Safety and Antiviral Effect of Multiple Doses of ABT-493 and ABT-530 in Adults With Genotype 1 Hepatitis C Virus (HCV)

Phase 2
Completed
Conditions
Compensated Cirrhosis
Chronic Hepatitis C
Hepatitis C Virus
Interventions
Drug: ABT-450/r/ABT-267, ABT-333
First Posted Date
2013-11-26
Last Posted Date
2021-07-12
Lead Sponsor
AbbVie
Target Recruit Count
89
Registration Number
NCT01995071
© Copyright 2025. All Rights Reserved by MedPath