Safety and Efficacy of Sofosbuvir/Velpatasvir/Voxilaprevir and Sofosbuvir/Velpatasvir in Adults With Chronic HCV Infection Who Have Not Previously Received Treatment With Direct-Acting Antiviral Therapy

PHASE3CompletedINTERVENTIONAL
Enrollment

943

Participants

Timeline

Start Date

November 16, 2015

Primary Completion Date

October 10, 2016

Study Completion Date

January 11, 2017

Conditions
Hepatitis C
Interventions
DRUG

SOF/VEL/VOX

400/100/100 mg tablet administered orally once daily with food

DRUG

SOF/VEL

400/100 mg tablet administered orally once daily with or without food

Trial Locations (93)

Unknown

Long Beach

Los Angeles

Palo Alto

Pasadena

Rialto

San Diego

San Francisco

Aurora

Englewood

Washington D.C.

Gainesville

Miami

Orlando

Wellington

Atlanta

Marietta

Chicago

Indianapolis

Bastrop

Baltimore

Catonsville

Boston

Ann Arbor

Detroit

Kansas City

St Louis

Hillsborough

Manhasset

New York

The Bronx

Asheville

Fayetteville

Philadelphia

Pittsburgh

Providence

Germantown

Knoxville

Nashville

Houston

Live Oak

San Antonio

Murray

Falls Church

Norfolk

Richmond

Seattle

Madison

Darlinghurst

Herston

Fitzroy

Melbourne

Perth

Calgary

Edmonton

Vancouver

Brampton

Ottawa

Toronto

Montreal

Bobigny

Clermont-Ferrand

Clichy

Créteil

Grenoble

Lille

Limoges

Lyon

Marseille

Montpellier

Nice

Orléans

Paris

Pessac

Rennes

Rouen

Strasbourg

Toulouse

Vandœuvre-lès-Nancy

Villejuif

Berlin

Bonn

Cologne

Frankfurt am Main

Hamburg

Hanover

Christchurch

Grafton

San Juan

London

Manchester

Nottingham

Oxford

Portsmouth

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY

NCT02607800 - Safety and Efficacy of Sofosbuvir/Velpatasvir/Voxilaprevir and Sofosbuvir/Velpatasvir in Adults With Chronic HCV Infection Who Have Not Previously Received Treatment With Direct-Acting Antiviral Therapy | Biotech Hunter | Biotech Hunter