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NCT01856426 · ClinicalTrials.gov registry record · Phase 1

Proof of Concept Study for Safety and Efficacy of EDP239 in Hepatitis C Subjects

A Phase 1 study of Hepatitis C, sponsored by Enanta Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
28
Enrollment target
5
Study locations

NCT01856426 is a Phase 1 study of Hepatitis C that has completed, run by Enanta Pharmaceuticals. The registered enrollment target is 28 participants, below the 1,890-participant average among 106 other Hepatitis C trials with a reported enrollment target (99% lower). The trial reports 5 study locations across 4 states.

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The verdict

NCT01856426, a Phase 1 study of Hepatitis C, has completed, sponsored by Enanta Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
28 participants
Enrollment target
5
Study locations

Study Summary

The purpose of this study is, to assess whether EDP239 can reduce the HCV viral load in HCV gentotype-1 in chronically infected subjects and to further evaluate the safety profile of EDP239.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG EDP239

Study Locations (5)

Other

  • Investigative Site - Frankfurt
  • Investigative Site - Hamburg

Florida

  • Investigative Site - Miami

Texas

  • Investigative Site - San Antonio

Utah

  • Investigative Site - Murray

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2013-06
Est. Completion 2015-10
Phase Phase 1

Sponsor

Enanta Pharmaceuticals

36 total trials

What the Registry Record Tells You About NCT01856426

The ClinicalTrials.gov registry entry for NCT01856426 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,890-participant average among 106 other Hepatitis C trials with a reported enrollment target (99% lower). The listed sponsor is Enanta Pharmaceuticals, which has 36 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.

NCT01856426 reports 5 study locations spanning 4 distinct geographic areas - top geographies include Other, Florida, Texas.

Frequently Asked Questions

What is clinical trial NCT01856426 about?

NCT01856426 is a clinical study titled "Proof of Concept Study for Safety and Efficacy of EDP239 in Hepatitis C Subjects". The purpose of this study is, to assess whether EDP239 can reduce the HCV viral load in HCV gentotype-1 in chronically infected subjects and to further evaluate the safety profile of EDP239.

What is the current status of trial NCT01856426?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2013-06. Estimated completion is 2015-10.

What conditions does trial NCT01856426 study?

This clinical trial studies the following conditions: Hepatitis C.

What interventions are being tested in trial NCT01856426?

The interventions under investigation include: Placebo (DRUG), EDP239 (DRUG).

Who is sponsoring clinical trial NCT01856426?

This trial is sponsored by Enanta Pharmaceuticals, which has 36 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01856426 being conducted?

This trial has 5 study locations across Florida, Texas, Utah. 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.