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

A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adults With Chronic Hepatitis C Virus Infection

Phase 3
Completed
Conditions
Chronic Hepatitis C Virus
Hepatitis C Virus
Interventions
First Posted Date
2016-03-14
Last Posted Date
2021-07-16
Lead Sponsor
AbbVie
Target Recruit Count
295
Registration Number
NCT02707952

A Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Liver or Post-Renal Transplant Recipients With Chronic Hepatitis C Virus (MAGELLAN-2)

Phase 3
Completed
Conditions
HCV
Hepatitis C Virus
Chronic Hepatitis C
Interventions
First Posted Date
2016-02-26
Last Posted Date
2021-07-13
Lead Sponsor
AbbVie
Target Recruit Count
100
Registration Number
NCT02692703

A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Renally Impaired Adults With Chronic Hepatitis C Virus Genotype 1 - 6 Infection

Phase 3
Completed
Conditions
Chronic Hepatitis C Virus (HCV) Infection
Interventions
First Posted Date
2016-01-08
Last Posted Date
2017-10-16
Lead Sponsor
AbbVie
Target Recruit Count
104
Registration Number
NCT02651194

A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C Virus Genotype 1, 2, 4, 5 or 6 Infection and Compensated Cirrhosis

Phase 3
Completed
Conditions
Compensated Cirrhosis
Chronic Hepatitis C
Hepatitis C Virus Infection
Interventions
First Posted Date
2015-12-30
Last Posted Date
2021-07-13
Lead Sponsor
AbbVie
Target Recruit Count
146
Registration Number
NCT02642432

A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C Virus (HCV) Genotype 2 Infection

Phase 3
Completed
Conditions
Chronic Hepatitis C Virus (HCV) Infection
Interventions
Drug: Placebo for ABT-493/ABT-530
First Posted Date
2015-12-29
Last Posted Date
2021-07-16
Lead Sponsor
AbbVie
Target Recruit Count
304
Registration Number
NCT02640482

A Study Comparing Efficacy and Safety of ABT-493/ABT-530 to Sofosbuvir Dosed With Daclatasvir in Adults With HCV Genotype 3 Infection

Phase 3
Completed
Conditions
Chronic Hepatitis C
Hepatitis C Virus
Genotype 3 Hepatitis C Virus
Interventions
First Posted Date
2015-12-28
Last Posted Date
2021-07-30
Lead Sponsor
AbbVie
Target Recruit Count
506
Registration Number
NCT02640157

The Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C Virus Genotype 4, 5, or 6 Infection (ENDURANCE-4)

Phase 3
Completed
Conditions
Hepatitis C Virus
Interventions
First Posted Date
2015-12-22
Last Posted Date
2021-07-13
Lead Sponsor
AbbVie
Target Recruit Count
121
Registration Number
NCT02636595

Treatment of Recently Acquired Hepatitis C With the 3D Regimen or G/P

Phase 3
Completed
Conditions
Hepatitis C, Acute
Interventions
First Posted Date
2015-12-17
Last Posted Date
2022-08-22
Lead Sponsor
Kirby Institute
Target Recruit Count
83
Registration Number
NCT02634008
Locations
🇦🇺

Royal Adelaide Hospital, Adelaide, South Australia, Australia

🇦🇺

St Vincent's Hospital, Sydney, New South Wales, Australia

🇬🇧

Pennine Acute Hospital, Manchester, United Kingdom

and more 8 locations

A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Subjects With Genotype 1 Infection

Phase 3
Completed
Conditions
HCV
Hepatitis C Virus
Chronic Hepatitis C
Interventions
First Posted Date
2015-11-13
Last Posted Date
2021-07-13
Lead Sponsor
AbbVie
Target Recruit Count
703
Registration Number
NCT02604017

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of ABT-493 and ABT-530 With and Without Ribavirin in Adults With HCV Who Failed a Prior DAA Containing Therapy

Phase 2
Completed
Conditions
Chronic Hepatitis C
Hepatitis C Virus
HCV
Direct-Acting Antiviral Agent (DAA)-Experienced
Interventions
First Posted Date
2015-05-18
Last Posted Date
2017-09-15
Lead Sponsor
AbbVie
Target Recruit Count
141
Registration Number
NCT02446717
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