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NCT01940471 · ClinicalTrials.gov registry record · Phase 3

Study to Compare Tenofovir Alafenamide (TAF) Versus Tenofovir Disoproxil Fumarate (TDF) in Participants With Chronic Hepatitis B Infection Who Are Positive for Hepatitis B e Antigen

A Phase 3 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 3
Development phase
875
Enrollment target

NCT01940471 is a Phase 3 study that has completed, run by Gilead Sciences. The registered enrollment target is 875 participants.

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The verdict

NCT01940471, a Phase 3 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 3
Development phase
875 participants
Enrollment target

Study Summary

The primary objective of this study is to compare the efficacy, safety, and tolerability of tenofovir alafenamide (TAF) versus tenofovir disoproxil fumarate (TDF) in treatment-naive and treatment-experienced adults with hepatitis B e antigen (HBeAg)-positive chronic hepatitis B virus (HBV) infection.

Interventions

  • DRUG TAF
  • DRUG TDF
  • DRUG TDF Placebo
  • DRUG TAF Placebo

Trial Details

FieldValue
Enrollment Target 875 participants
Start Date 2013-09-11
Est. Completion 2022-10-13
Phase Phase 3

Sponsor

Gilead Sciences

504 total trials

What the Registry Record Tells You About NCT01940471

The ClinicalTrials.gov registry entry for NCT01940471 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 875 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 4 interventions - of which TAF is the first listed.

NCT01940471 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01940471 about?

NCT01940471 is a clinical study titled "Study to Compare Tenofovir Alafenamide (TAF) Versus Tenofovir Disoproxil Fumarate (TDF) in Participants With Chronic Hepatitis B Infection Who Are Positive for Hepatitis B e Antigen". The primary objective of this study is to compare the efficacy, safety, and tolerability of tenofovir alafenamide (TAF) versus tenofovir disoproxil fumarate (TDF) in treatment-naive and treatment-experienced adults with hepatitis B e antigen (HBeAg)-positive chronic hepatitis B virus (HBV) infection...

What is the current status of trial NCT01940471?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 875 participants. The study started on 2013-09-11. Estimated completion is 2022-10-13.

What interventions are being tested in trial NCT01940471?

The interventions under investigation include: TAF (DRUG), TDF (DRUG), TDF Placebo (DRUG), TAF Placebo (DRUG).

Who is sponsoring clinical trial NCT01940471?

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.