TheraRadar

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Data updated: Mar 10, 2026

VOSEVI

SOFOSBUVIR RNA Replicase Inhibitors
Infectious Disease Approved 2017-07-18
2
Indications
--
Phase 3 Trials
1
Priority Reviews
8
Years on Market

Details

Status
Prescription
First Approved
2017-07-18
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: SOFOSBUVIR , VELPATASVIR , VOXILAPREVIR

VOSEVI Approval History

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What VOSEVI Treats

1 indications

VOSEVI 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

VOSEVI 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 VOSEVI. HBV reactivation has been reported in HCV/HBV coinfected patients who were undergoing or had completed treatment with HCV direct-acting antivirals (DAA) and were not receiving HBV antiviral therapy. Some cases have resulted in fulminant hepatitis, hepatic failure, and death. Monitor HCV/HBV coi...

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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.

VOSEVI FDA Label Details

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Indications & Usage

FDA Label (PDF)

VOSEVI is indicated for the treatment of adult patients with chronic hepatitis C virus (HCV) infection without cirrhosis or with compensated cirrhosis (Child-Pugh A) who have [see Dosage and Administration and Clinical Studies ]: genotype 1, 2, 3, 4, 5, or 6 infection and have previously been treated with an HCV regimen containing an NS5A inhibitor. genotype 1a or 3 infection and have previously been treated with an HCV regimen containing sofosbuvir without an NS5A inhibitor. Additional benefit of VOSEVI over sofosbuvir/velpatasvir was not shown in adults with genotype 1b, 2, 4, 5, or 6 infect...

⚠️ 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 VOSEVI. HBV reactivation has been reported in HCV/HBV coinfected patients who were undergoing ...

VOSEVI Patents & Exclusivity

Latest Patent: Nov 2037

Patents (47 active)

US11338007*PED Expires Dec 1, 2037
US11338007 Expires Jun 1, 2037
US10912814 Expires Jun 1, 2037
US11116783*PED Expires Jul 30, 2034
US9296782 Expires Jul 17, 2034
US11116783 Expires Jan 30, 2034
US8575135*PED Expires May 16, 2033
US8921341*PED Expires May 16, 2033
US8940718*PED Expires May 16, 2033
US8940718 Expires Nov 16, 2032
+ 37 more patents
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.