ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Single Dose vs. Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections

ClinicalTrials.gov ID: NCT02127970

Public ClinicalTrials.gov record NCT02127970. 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 May 19, 2026, 7:52 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 3b, Double-Blind, Multicenter, Randomized Study to Compare the Efficacy and Safety of Single Dose Dalbavancin to a Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections

Study identification

NCT ID
NCT02127970
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Durata Therapeutics Inc., an affiliate of Allergan plc
Industry
Enrollment
698 participants

Conditions and interventions

Interventions

  • Dalbavancin Drug
  • Dalbavancin-matching Placebo Drug

Drug

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
Apr 17, 2014
Primary completion
Mar 10, 2015
Completion
Mar 10, 2015
Last update posted
Sep 27, 2018

2014 – 2015

United States locations

U.S. sites
25
U.S. states
12
U.S. cities
21
Facility City State ZIP Site status
110 Montgomery Alabama 36106
103 Anaheim California 92804
117 Long Beach California 90806
106 Long Beach California 90813
118 Modesto California 95350
104 San Diego California 92120
113 San Diego California 92120
115 San Diego California 92120
116 San Diego California 92120
108 Stockton California 95204
105 Sylmar California 91342
112 Washington D.C. District of Columbia 20037
107 Orlando Florida 32806
120 Saint Cloud Florida 34769
114 Augusta Georgia 30909
122 Columbus Georgia 31904
125 Savannah Georgia 31405
119 Eunice Louisiana 70535
101 Springfield Massachusetts 01199
109 Detroit Michigan 48202
121 Butte Montana 59701
123 Omaha Nebraska 68131
111 Toledo Ohio 43608
126 Franklin Tennessee 37064
127 Smyrna Tennessee 37167

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 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02127970, 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 Sep 27, 2018 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02127970 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →