Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)

18 total trials 18 completed

Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) sponsors 18 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 18 completed. 2 of these trials are in Phase 3-4 (later-stage) and 16 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Healthy Subjects, with 1 trials.

Trial Pipeline

18 total, page 1 of 1

COMPLETED Phase 1

A Phase 1, Open-Label, 10 Day Safety Study

NCT01623401

COMPLETED Phase 1

A Phase 1 Crossover Study of Blood Pressure and Heart Rate Response

NCT01577459

COMPLETED Phase 2

A Phase 2 Safety and Exploratory Skin Lesion Measurement of TR-701 FA Study

NCT01519778

COMPLETED Phase 1

A Phase 1 TR-701 FA Study of Blood Pressure Response Post Tyramine Challenge

NCT01539473

COMPLETED Phase 1

Pharmacokinetics, Safety, and Tolerability of TR-701 Free Acid (FA) in Elderly Subjects

NCT01496677

COMPLETED Phase 1

A Thorough QT Study of TR-701free Acid (FA) in Healthy Subjects

NCT01461460

COMPLETED Phase 1

A Pharmacokinetics and Safety Study in Subjects With Renal Impairment

NCT01452828

COMPLETED Phase 3

TR-701 FA vs Linezolid for the Treatment of Acute Bacterial Skin and Skin Structure Infections

NCT01421511

COMPLETED Phase 1

A PK and Safety Study in Subjects With Hepatic Impairment

NCT01431833

COMPLETED Phase 1

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

NCT01271998

COMPLETED Phase 1

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

NCT01442831

COMPLETED Phase 3

TR-701 FA vs. Linezolid for the Treatment of Acute Bacterial Skin and Skin Structure Infections.

NCT01170221

COMPLETED Phase 1

Ascending Dose Pharmacokinetic (PK) and Absolute Bioavailability (BA)

NCT00983255

COMPLETED Phase 1

Exploratory Pharmacokinetic and Bioavailability Study of 2 Capsule Formulations of Torezolid Phosphate

NCT00876655

COMPLETED Phase 2

Phase 2 Study of TR-701 in Patients With Complicated Skin and Skin Structure Infections

NCT00761215

COMPLETED Phase 1

Microdialysis and Pharmacokinetic Study of TR-701

NCT00666601

COMPLETED Phase 1

Food Effects of Single Oral Dose of 600mg TR-701

NCT00671359

COMPLETED Phase 1

Single and Multiple Ascending Dose Pharmacokinetic Study of TR701 in Healthy Adults

NCT00671814

Phase Distribution

PhaseTrial count
Phase 1 14
Phase 2 2
Phase 3 2

Therapeutic Areas

What the Pipeline for Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) Shows

According to the ClinicalTrials.gov registry, Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) is linked to 18 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 18 are already marked complete, representing roughly 100% of the total.

The phase mix for Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) reports 2 late-stage studies (Phase 3 and Phase 4 combined) and 16 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) is Healthy Subjects with 1 linked trial, and 0 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

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 aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.