TheraRadar

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Data updated: Mar 10, 2026

MAVYRET

GLECAPREVIR HCV NS3/4A Protease Inhibitors
Infectious Disease Approved 2017-08-03
7
Indications
--
Phase 3 Trials
4
Priority Reviews
8
Years on Market

Details

Status
Prescription
First Approved
2017-08-03
Routes
ORAL
Dosage Forms
PELLETS, TABLET

Companies

Active Ingredient: GLECAPREVIR , PIBRENTASVIR

MAVYRET Approval History

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What MAVYRET Treats

1 indications

MAVYRET is approved for 1 conditions since its original approval in 2017. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Hepatitis C
Source: FDA Label

MAVYRET Boxed Warning

RISK OF HEPATITIS B VIRUS REACTIVATION IN PATIENTS COINFECTED WITH HCV AND HBV Test all patients for evidence of current or prior hepatitis B virus (HBV) infection before initiating treatment with MAVYRET. HBV reactivation has been reported in HCV/HBV coinfected patients who were undergoing or had completed treatment with HCV direct-acting antivirals and were not receiving HBV antiviral therapy. Some cases have resulted in fulminant hepatitis, hepatic failure, and death. Monitor HCV/HBV coinfect...

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

MAVYRET FDA Label Details

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Indications & Usage

FDA Label (PDF)

MAVYRET is indicated for the treatment of adult and pediatric patients 3 years and older with acute or 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 indicated for the treatment of adult and pediatric patients 3 years and older 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 [see Dosage and Administration and Clinical Studies ]. MAVYRET is a fixed-dose combination of glecaprevir, a he...

⚠️ BOXED WARNING

WARNING: RISK OF HEPATITIS B VIRUS REACTIVATION IN PATIENTS COINFECTED WITH HCV AND HBV Test all patients for evidence of current or prior hepatitis B virus (HBV) infection before initiating treatment with MAVYRET. HBV reactivation has been reported in HCV/HBV coinfected patients who were undergoing...

MAVYRET Patents & Exclusivity

Latest Patent: Dec 2036
Exclusivity: Dec 2028

Patents (51 active)

US11246866*PED Expires Dec 24, 2036
US11246866 Expires Jun 24, 2036
US9321807*PED Expires Dec 5, 2035
USRE48923*PED Expires Nov 8, 2035
US9321807 Expires Jun 5, 2035
USRE48923 Expires May 8, 2035
US10286029*PED Expires Sep 14, 2034
US11484534*PED Expires Sep 14, 2034
US10286029 Expires Mar 14, 2034
US11484534 Expires Mar 14, 2034
+ 41 more patents

Exclusivity

I-967 Until Jun 2028
ODE-372 Until Jun 2028
PED Until Dec 2028
I-967 Until Jun 2028
ODE-232 Until Apr 2026
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.