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Completed Phase 2 Interventional

Efficacy and Safety of NVC-422 in the Treatment of Adenoviral Conjunctivitis

ClinicalTrials.gov ID: NCT01532336

Public ClinicalTrials.gov record NCT01532336. 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 Jun 26, 2026, 11:38 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 NVC-422 Ophthalmic Solution for the Treatment of Adenoviral Conjunctivitis

Study identification

NCT ID
NCT01532336
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
NovaBay Pharmaceuticals, Inc.
Industry
Enrollment
500 participants

Conditions and interventions

Interventions

  • NVC-422 Solution, 0.3% Drug
  • NVC-422 Vehicle Solution Drug

Drug

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
Apr 30, 2012
Primary completion
Apr 30, 2014
Completion
Jul 31, 2014
Last update posted
May 27, 2015

2012 – 2014

United States locations

U.S. sites
24
U.S. states
13
U.S. cities
24
Facility City State ZIP Site status
Not listed Glendale California 91205
Not listed Los Angeles California 90048
Not listed Petaluma California 94954
Not listed San Diego California 92115
Not listed Fort Myers Florida 33901
Not listed Jacksonville Beach Florida 32250
Not listed Tampa Florida 33603
Not listed Albany Georgia 31701
Not listed Kailua Hawaii 96734
Not listed Glenview Illinois 60026
Not listed Peoria Illinois 61615
Not listed Shawnee Mission Kansas 66204
Not listed Hazard Kentucky 41701
Not listed Winchester Massachusetts 01890
Not listed Kansas City Missouri 64154
Not listed St Louis Missouri 63131
Not listed Hicksville New York 11801
Not listed Rockville Centre New York 11570
Not listed Asheville North Carolina 28803
Not listed High Point North Carolina 27262
Not listed Winston-Salem North Carolina 27101
Not listed Pittsburgh Pennsylvania 15206
Not listed Charleston South Carolina 29414
Not listed Spartanburg South Carolina 29306

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 34 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01532336, 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 Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01532336 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →