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NCT01999725 · ClinicalTrials.gov registry record · Phase 1

Evaluation of the Safety and Pharmacokinetics of a Single Oral Dose of EDP-788

A Phase 1 study, sponsored by Enanta Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
80
Enrollment target

NCT01999725 is a Phase 1 study that has completed, run by Enanta Pharmaceuticals. The registered enrollment target is 80 participants.

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The verdict

NCT01999725, a Phase 1 study, has completed, sponsored by Enanta Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
80 participants
Enrollment target

Study Summary

The primary objective of the study is to determine the safety of single doses of orally administered EDP-788. Secondary objectives of the study are: * To describe the pharmacokinetics of EDP-788 (and its metabolite EDP-322) after single doses of orally administered drug * To estimate the bioavailability of EDP-788 capsules relative to an oral liquid suspension * To estimate the effect of co-administration of food on the absorption of EDP-788

Interventions

  • DRUG Placebo
  • DRUG EDP-788

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2014-01
Est. Completion 2014-09
Phase Phase 1

Sponsor

Enanta Pharmaceuticals

36 total trials

What the Registry Record Tells You About NCT01999725

The ClinicalTrials.gov registry entry for NCT01999725 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Enanta Pharmaceuticals, which has 36 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01999725 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01999725 about?

NCT01999725 is a clinical study titled "Evaluation of the Safety and Pharmacokinetics of a Single Oral Dose of EDP-788". The primary objective of the study is to determine the safety of single doses of orally administered EDP-788. Secondary objectives of the study are: * To describe the pharmacokinetics of EDP-788 (and its metabolite EDP-322) after single doses of orally administered drug * To estimate the bioavaila...

What is the current status of trial NCT01999725?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2014-01. Estimated completion is 2014-09.

What interventions are being tested in trial NCT01999725?

The interventions under investigation include: Placebo (DRUG), EDP-788 (DRUG).

Who is sponsoring clinical trial NCT01999725?

This trial is sponsored by Enanta Pharmaceuticals, which has 36 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.