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NCT01924949 · ClinicalTrials.gov registry record · Phase 2

Ledipasvir/Sofosbuvir Fixed-Dose Combination in Adults With Nosocomial Genotype 1 HCV Infection

A Phase 2 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 2
Development phase
5
Enrollment target

NCT01924949 is a Phase 2 study that has completed, run by Gilead Sciences. The registered enrollment target is 5 participants.

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The verdict

NCT01924949, a Phase 2 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

This study is to evaluate the antiviral efficacy, safety, and tolerability of ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) in adults with nosocomial genotype 1 hepatitis C virus (HCV) infection.

Interventions

  • DRUG LDV/SOF

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2013-07
Est. Completion 2014-08
Phase Phase 2

Sponsor

Gilead Sciences

504 total trials

What the Registry Record Tells You About NCT01924949

The ClinicalTrials.gov registry entry for NCT01924949 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 5 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 LDV/SOF is the first listed.

NCT01924949 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01924949 about?

NCT01924949 is a clinical study titled "Ledipasvir/Sofosbuvir Fixed-Dose Combination in Adults With Nosocomial Genotype 1 HCV Infection". This study is to evaluate the antiviral efficacy, safety, and tolerability of ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) in adults with nosocomial genotype 1 hepatitis C virus (HCV) infection.

What is the current status of trial NCT01924949?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2013-07. Estimated completion is 2014-08.

What interventions are being tested in trial NCT01924949?

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

Who is sponsoring clinical trial NCT01924949?

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.