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NCT01271998 · ClinicalTrials.gov registry record · Phase 1

Pulmonary Disposition of TR-700 Following Once-Daily Oral 200 mg

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
20
Enrollment target

NCT01271998: Completed Phase 1 study, sponsored by Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA).

NCT01271998 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 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01271998, 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
20 participants
Enrollment target

Study Summary

The primary purpose of this study is to determine the steady-state plasma pharmacokinetics (PK) and properties of TR-700 into the pulmonary epithelial lining fluid (ELF) and alveolar macrophages (AM) of healthy volunteers.

Primary Outcome

Pharmacokinetic parameters compared with baseline measurements.

Interventions

  • DRUG TR-701 FA

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2010-12-08
Est. Completion 2011-01-03
Phase Phase 1

What the finished NCT01271998 record still lists

NCT01271998 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 1 intervention - of which TR-701 FA is the first listed.

NCT01271998 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01271998 about?

NCT01271998 is a clinical study titled "Pulmonary Disposition of TR-700 Following Once-Daily Oral 200 mg". The primary purpose of this study is to determine the steady-state plasma pharmacokinetics (PK) and properties of TR-700 into the pulmonary epithelial lining fluid (ELF) and alveolar macrophages (AM) of healthy volunteers.

What is the current status of trial NCT01271998?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2010-12-08. Estimated completion is 2011-01-03.

What interventions are being tested in trial NCT01271998?

The interventions under investigation include: TR-701 FA (DRUG).

Who is sponsoring clinical trial NCT01271998?

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.

How this trial's enrollment target compares

Where NCT01271998's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01271998, the US trial registry maintained by the National Library of Medicine. NCT01271998 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.