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

Overview

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

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/06/27
Not Applicable
Not yet recruiting
2022/12/06
Phase 2
Recruiting
2022/10/17
Phase 4
Terminated
2022/07/07
Phase 2
Completed
2021/11/05
Not Applicable
Completed
2020/12/23
Early Phase 1
Completed
2020/11/03
Phase 4
Withdrawn
2020/10/05
Phase 4
Completed
2020/08/17
Phase 4
Terminated
2020/08/11
Phase 4
Active, not recruiting

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
AbbVie Inc.
0074-2600
ORAL
50 mg in 1 1
10/31/2023
AbbVie Inc.
0074-2625
ORAL
100 mg in 1 1
10/31/2023

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
Authorised
7/26/2017

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
MAVIRET FILM-COATED TABLET 100MG/40MG
SIN15603P
TABLET, FILM COATED
100.0 mg
12/26/2018

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

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