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NCT03118843 · ClinicalTrials.gov registry record · Phase 3

Safety And Efficacy of Sofosbuvir/Velpatasvir/Voxilaprevir Fixed-Dose Combination for 12 Weeks in Adults Who Participated in a Prior Gilead-Sponsored HCV Treatment Study

A Phase 3 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 3
Development phase
31
Enrollment target

NCT03118843 is a Phase 3 study that has completed, run by Gilead Sciences. The registered enrollment target is 31 participants.

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The verdict

NCT03118843, a Phase 3 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 3
Development phase
31 participants
Enrollment target

Study Summary

The primary objectives of this study are to determine the efficacy, safety, and tolerability of treatment with sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) fixed-dose combination (FDC) for 12 weeks in participants with chronic hepatitis C virus (HCV) infection with or without cirrhosis, who did not achieve sustained viral response (SVR) after receiving prior treatment in a Gilead-sponsored HCV treatment study of direct-acting antiviral (DAA)-containing regimens.

Interventions

  • DRUG SOF/VEL/VOX

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2017-04-25
Est. Completion 2018-03-19
Phase Phase 3

Sponsor

Gilead Sciences

504 total trials

What the Registry Record Tells You About NCT03118843

The ClinicalTrials.gov registry entry for NCT03118843 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gilead Sciences, which has 504 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which SOF/VEL/VOX is the first listed.

NCT03118843 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03118843 about?

NCT03118843 is a clinical study titled "Safety And Efficacy of Sofosbuvir/Velpatasvir/Voxilaprevir Fixed-Dose Combination for 12 Weeks in Adults Who Participated in a Prior Gilead-Sponsored HCV Treatment Study". The primary objectives of this study are to determine the efficacy, safety, and tolerability of treatment with sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) fixed-dose combination (FDC) for 12 weeks in participants with chronic hepatitis C virus (HCV) infection with or without cirrhosis, who did...

What is the current status of trial NCT03118843?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 31 participants. The study started on 2017-04-25. Estimated completion is 2018-03-19.

What interventions are being tested in trial NCT03118843?

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

Who is sponsoring clinical trial NCT03118843?

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

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.