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. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
MAVIRET glecaprevir/pibrentasvir 100 mg/40 mg film-coated tablet blister pack | 284948 | Medicine | A | 1/2/2018 | |
MAVIRET glecaprevir/pibrentasvir 100 mg/40 mg film-coated tablet bottle | 325401 | Medicine | A | 1/16/2020 | |
MAVIRET glecaprevir 50 mg / pibrentasvir 20 mg granules sachet | 352573 | Medicine | A | 2/7/2022 |
Help Us Improve
Your feedback helps us provide better drug information and insights.