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NCT01442831 · ClinicalTrials.gov registry record · Phase 1

Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects

A Phase 1 study, sponsored by Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA).

Completed
Registry status
Phase 1
Development phase
6
Enrollment target

NCT01442831 is a Phase 1 study that has completed, run by Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA). The registered enrollment target is 6 participants.

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The verdict

NCT01442831, a Phase 1 study, has completed, sponsored by Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA).

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

The purpose of this study is to describe the single dose pharmacokinetics of total radioactivity in plasma and whole blood following PO administration of \[14C\] TR-701 in healthy adult male subjects.

Interventions

  • DRUG Human ADME

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2010-09-09
Est. Completion 2010-09-22
Phase Phase 1

What the Registry Record Tells You About NCT01442831

The ClinicalTrials.gov registry entry for NCT01442831 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 18 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Human ADME is the first listed.

NCT01442831 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01442831 about?

NCT01442831 is a clinical study titled "Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects". The purpose of this study is to describe the single dose pharmacokinetics of total radioactivity in plasma and whole blood following PO administration of \[14C\] TR-701 in healthy adult male subjects.

What is the current status of trial NCT01442831?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2010-09-09. Estimated completion is 2010-09-22.

What interventions are being tested in trial NCT01442831?

The interventions under investigation include: Human ADME (DRUG).

Who is sponsoring clinical trial NCT01442831?

This trial is sponsored by Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 18 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.