Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections

ClinicalTrials.gov ID: NCT01431339

Public ClinicalTrials.gov record NCT01431339. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 6:18 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Double-Blind, Double-Dummy Study to Compare the Efficacy and Safety of Dalbavancin to a Comparator Regimen (Vancomycin and Linezolid) for the Treatment of Acute Bacterial Skin and Skin Structure Infections

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary object is to compare the early clinical efficacy (after 48-72 hours of therapy) of dalbavancin to the comparator regimen (vancomycin with the option to switch to oral linezolid) for the treatment of patients with a suspected or proved gram-positive bacterial skin or skin structure infections.

Study identification

NCT ID
NCT01431339
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
739 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2011 (Type not available)
Primary completion
Nov 2012 (Actual)
Completion
Dec 2012 (Actual)
Last update posted
Feb 12, 2014

2011 – 2012

United States locations

U.S. sites
30
U.S. states
11
U.S. cities
29
Facility City State ZIP Site status
Durata Clinical Site Montgomery Alabama 36106 —
Durata Clinical Site Anaheim California 92804 —
Durata Clinical Site Buena Park California 90620 —
Durata Study Site Chula Vista California 91911 —
Durata Clinical Site Long Beach California 90813 —
Durata Study Site Los Angeles California 90015 —
Durata Study Site Norwalk California 90650 —
Durata Study Site Oxnard California 93030 —
Durata Study SIte San Diego California 92120 —
Durata Study Site Stockton California 95204 —
Durata Clinical Site Boyton Beach Florida 33435 —
Durata Clinical Site Fort Meyers Florida 33966 —
Durata Clinical Site Miami Florida 33015 —
Durata Study Site Orlando Florida 32837 —
Durata Clinical Site Saint Cloud Florida 34769 —
Durata Clinical Site Augusta Georgia 30901 —
Durata Study Site Columbus Georgia 31904 —
Durata Clinical Site Chicago Illinois 60637 —
Durata Study Site Baton Rouge Louisiana 70809 —
Durata Study Site New Orleans Louisiana 70112 —
Durata Study Site Shreveport Louisiana 71101 —
Durata Study Site Zachary Louisiana 70791 —
Durata Study Site Las Vegas Nevada 89109 —
Durata Study Site Springfield Ohio 45502 —
Durata Study Site Philadelphia Pennsylvania 19103 —
Durata Study Site Austin Texas 78701 —
Durata Clinical Site Austin Texas 78752 —
Durata Clinical Site Houston Texas 77055 —
Durata Study Site Richmond Texas 77469 —
Durata Study Site Middleton Wisconsin 53562 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 107 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01431339, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 12, 2014 · Synced Oct 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01431339 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →