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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 Oct 24, 2026, 9:22 PM 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

Brief summary

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

To compare the efficacy of treatment with a single dose of dalbavancin 1500 mg to treatment with a two dose regimen of dalbavancin (1000 mg on Day 1 followed by 500 mg on Day 8) in participants with known or suspected Gram-positive acute bacterial skin and skin structure infections (ABSSSI) at 48 -72 hours after initiation of treatment.

Study identification

NCT ID
NCT02127970
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
698 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
Apr 18, 2014 (Actual)
Primary completion
Mar 11, 2015 (Actual)
Completion
Mar 11, 2015 (Actual)
Last update posted
Sep 28, 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 28, 2018 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02127970 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →