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Completed Phase 2 Interventional

Efficacy and Safety of Auriclosene (NVC-422) in the Treatment of Bacterial Conjunctivitis

ClinicalTrials.gov ID: NCT01877694

Public ClinicalTrials.gov record NCT01877694. 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 Sep 5, 2026, 2:35 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 Multicenter, Randomized Study of the Efficacy and Safety of Auriclosene (NVC-422) Ophthalmic Solution 0.3% for the Treatment of Bacterial Conjunctivitis

Brief summary

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

The purpose of this study is to evaluate the microbiological and clinical efficacy of Auriclosene compared to its vehicle for bacterial conjunctivitis. Adults and children one year of age and older with bacterial conjunctivitis in at least one eye may be eligible. Subjects will be randomly assigned to receive either Auriclosene Ophthalmic Solution or Vehicle Ophthalmic Solution.

Study identification

NCT ID
NCT01877694
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
NovaBay Pharmaceuticals, Inc.
Industry
Enrollment
217 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Year and older
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
May 31, 2013
Primary completion
Nov 30, 2014
Completion
Dec 31, 2014
Last update posted
May 27, 2015

2013 – 2015

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Not listed Birmingham Alabama 35244
Not listed Phoenix Arizona 85032
Not listed Anaheim California 92804
Not listed Bellflower California 90706
Not listed Glendale California 91204
Not listed Huntington Beach California 92647
Not listed Clearwater Florida 33761
Not listed Woodstock Georgia 30189
Not listed Evansville Indiana 47714
Not listed Newton Kansas 67114
Not listed Whitehouse Station New Jersey 08889
Not listed Huntersville North Carolina 28078
Not listed Winston-Salem North Carolina 27101
Not listed Cincinnati Ohio 45246
Not listed Dayton Ohio 45432
Not listed Corsicana Texas 75110
Not listed San Antonio Texas 78215
Not listed Clinton Utah 84015
Not listed Charlottesville Virginia 22902
Not listed Midlothian Virginia 23113
Not listed Spokane Washington 99202

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01877694, 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 May 27, 2015 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01877694 live on ClinicalTrials.gov.

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