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NCT02607735 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy of Sofosbuvir/Velpatasvir/Voxilaprevir in Adults With Chronic HCV Infection Who Have Previously Received Treatment With Direct-Acting Antiviral Therapy

A Phase 3 study of Hepatitis C, sponsored by Gilead Sciences.

Completed
Registry status
Phase 3
Development phase
416
Enrollment target
20
Study locations

NCT02607735 is a Phase 3 study of Hepatitis C that has completed, run by Gilead Sciences. The registered enrollment target is 416 participants, below the 1,886-participant average among 106 other Hepatitis C trials with a reported enrollment target (78% lower). The trial reports 20 study locations across 8 states.

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The verdict

NCT02607735, a Phase 3 study of Hepatitis C, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 3
Development phase
416 participants
Enrollment target
20
Study locations

Study Summary

The primary objectives of this study are to evaluate the safety and efficacy of treatment with sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) in adults with chronic hepatitis C virus (HCV) infection who have previously received treatment with direct-acting antiviral therapy. Participants randomized to placebo may be eligible for deferred treatment with active SOF/VEL/VOX.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG SOF/VEL/VOX

Study Locations (20)

California

  • - Long Beach
  • - Los Angeles
  • - Palo Alto
  • - Pasadena
  • - Rialto
  • - San Diego
  • - San Francisco

Florida

  • - Gainesville
  • - Miami
  • - Orlando
  • - Wellington

Colorado

  • - Aurora
  • - Englewood

Georgia

  • - Atlanta
  • - Marietta

Maryland

  • - Baltimore
  • - Catonsville

District of Columbia

  • - Washington D.C.

Illinois

  • - Chicago

Indiana

  • - Indianapolis

Trial Details

FieldValue
Enrollment Target 416 participants
Start Date 2015-11-11
Est. Completion 2017-06-21
Phase Phase 3

Sponsor

Gilead Sciences

504 total trials

What the Registry Record Tells You About NCT02607735

The ClinicalTrials.gov registry entry for NCT02607735 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 416 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,886-participant average among 106 other Hepatitis C trials with a reported enrollment target (78% lower). The listed sponsor is Gilead Sciences, which has 504 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hepatitis C appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT02607735 reports 20 study locations spanning 8 distinct geographic areas - top geographies include California, Florida, Colorado.

Frequently Asked Questions

What is clinical trial NCT02607735 about?

NCT02607735 is a clinical study titled "Safety and Efficacy of Sofosbuvir/Velpatasvir/Voxilaprevir in Adults With Chronic HCV Infection Who Have Previously Received Treatment With Direct-Acting Antiviral Therapy". The primary objectives of this study are to evaluate the safety and efficacy of treatment with sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) in adults with chronic hepatitis C virus (HCV) infection who have previously received treatment with direct-acting antiviral therapy. Participants randomi...

What is the current status of trial NCT02607735?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 416 participants. The study started on 2015-11-11. Estimated completion is 2017-06-21.

What conditions does trial NCT02607735 study?

This clinical trial studies the following conditions: Hepatitis C.

What interventions are being tested in trial NCT02607735?

The interventions under investigation include: Placebo (DRUG), SOF/VEL/VOX (DRUG).

Who is sponsoring clinical trial NCT02607735?

This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02607735 being conducted?

This trial has 20 study locations across California, Colorado, District of Columbia, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.