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Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination ± Ribavirin for the Treatment of HCV (ION-3)

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Gilead Sciences

Status and phase

Completed
Phase 3

Conditions

Chronic Hepatitis C Virus

Treatments

Drug: LDV/SOF
Drug: RBV

Study type

Interventional

Funder types

Industry

Identifiers

NCT01851330
GS-US-337-0108

Details and patient eligibility

About

This study is to evaluate the safety, tolerability, and antiviral efficacy of ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) with or without ribavirin (RBV) administered for 8 or 12 weeks in treatment-naive participants with chronic genotype 1 HCV infection.

Enrollment

647 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18, with chronic genotype 1 HCV infection
  • HCV treatment-naive
  • HCV RNA > 10,000 IU/mL at screening
  • Screening laboratory values within defined thresholds
  • Use of two effective contraception methods if female of childbearing potential or sexually active male

Exclusion criteria

  • Pregnant or nursing female or male with pregnant female partner
  • Presence of cirrhosis
  • Coinfection with HIV or hepatitis B virus (HBV)
  • Current or prior history of clinical hepatic decompensation
  • Chronic use of systemic immunosuppressive agents
  • History of clinically significant illness or any other medical disorder that may interfere with subject treatment, assessment or compliance with the protocol

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

647 participants in 3 patient groups

LDV/SOF 8 Week
Experimental group
Description:
Participants will receive LDV/SOF FDC for 8 weeks.
Treatment:
Drug: LDV/SOF
LDV/SOF+RBV 8 Week
Experimental group
Description:
Participants will receive LDV/SOF FDC plus RBV for 8 weeks.
Treatment:
Drug: RBV
Drug: LDV/SOF
LDV/SOF 12 Week
Experimental group
Description:
Participants will receive LDV/SOF FDC for 12 weeks.
Treatment:
Drug: LDV/SOF

Trial contacts and locations

52

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Data sourced from clinicaltrials.gov

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