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NCT01175707 · ClinicalTrials.gov registry record · Phase 4

Study Comparing Cubicin With Vancomycin in Treatment of Participants With Complicated Skin and Skin Structure Infections in a Home Infusion Setting

A Phase 4 study, sponsored by Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA).

Terminated
Registry status
Phase 4
Development phase
80
Enrollment target

NCT01175707 is a Phase 4 study that was terminated before completion, run by Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA). The registered enrollment target is 80 participants.

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The verdict

NCT01175707, a Phase 4 study, was terminated before completion, sponsored by Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA).

TERMINATED
Registry status
Phase 4
Development phase
80 participants
Enrollment target

Study Summary

This is a randomized, open-label, multi-center, phase 4 study designed to compare intravenous (IV) daptomycin and IV vancomycin administered in a home infusion setting for the treatment of complicated skin and skin structure infections (cSSSI) due to Gram-positive bacteria in participants who are prescribed vancomycin for 7 to 14 days and who are planning to receive vancomycin in a home-infusion setting.

Interventions

  • DRUG Vancomycin
  • DRUG Daptomycin

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2010-07-15
Est. Completion 2011-11-17
Phase Phase 4

What the Registry Record Tells You About NCT01175707

The ClinicalTrials.gov registry entry for NCT01175707 describes a study currently listed as terminated, categorized as Phase 4. 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 Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 42 total studies on file at ClinicalTrials.gov.

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

NCT01175707 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01175707 about?

NCT01175707 is a clinical study titled "Study Comparing Cubicin With Vancomycin in Treatment of Participants With Complicated Skin and Skin Structure Infections in a Home Infusion Setting". This is a randomized, open-label, multi-center, phase 4 study designed to compare intravenous (IV) daptomycin and IV vancomycin administered in a home infusion setting for the treatment of complicated skin and skin structure infections (cSSSI) due to Gram-positive bacteria in participants who are pr...

What is the current status of trial NCT01175707?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 80 participants. The study started on 2010-07-15. Estimated completion is 2011-11-17.

What interventions are being tested in trial NCT01175707?

The interventions under investigation include: Vancomycin (DRUG), Daptomycin (DRUG).

Who is sponsoring clinical trial NCT01175707?

This trial is sponsored by Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 42 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.