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Completed Phase 2 Interventional Results available

To Assess the Safety and Efficacy of R932348 Ophthalmic Solutions in Patients With Keratoconjunctivitis Sicca

ClinicalTrials.gov ID: NCT01900249

Public ClinicalTrials.gov record NCT01900249. 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 Jul 21, 2026, 6:49 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 2, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of 0.2% and 0.5% R932348 Ophthalmic Solutions in Patients With Keratoconjunctivitis Sicca

Study identification

NCT ID
NCT01900249
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Rigel Pharmaceuticals
Industry
Enrollment
204 participants

Conditions and interventions

Interventions

  • R348 Ophthalmic Solution, 0.2% Drug
  • R348 Ophthalmic Solution, 0.5% Drug
  • 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
Jun 30, 2013
Primary completion
Jun 30, 2014
Completion
Jun 30, 2014
Last update posted
Oct 2, 2016

2013 – 2014

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
Sall Research Medical Center Artesia California 90701
North Bay Eye Petaluma California 94954
Martel Medical Eye Group Rancho Cardova California 95670
Specialty Eye Care Parker Colorado 808134
International Research Center Brandon Florida 33603
East Florida Eye Institute Stuart Florida 34994
Clayton Eye Center Morrow Georgia 30260
Coastal Research Associates Roswell Georgia 30076
Chicago Research Center Chicago Illinois 60634
Chicago Cornea Consultants Hoffman Estates Illinois 60169
Koffler Vision Group Lebanon Kentucky 40033
Taustine Eye Center Louisville Kentucky 40217
Comprehensive Eye Care, Ltd/Vision Research Institute, LLC Washington Missouri 63090
Mundorf Eye Center Charlotte North Carolina 28204
Charlotte Eye Ear Nose and Throat Associates, PA Charlotte North Carolina 28210
Cornerstone Eyecare High Point North Carolina 27262
Abrams Eye Center Cleveland Ohio 44115
Glaucoma Consultants and Center for Eye Research Mt. Pleasant South Carolina 29464
Chattanooga Eye Institute Chattanooga Tennessee 37411
Eye Clinics of South Texas San Antonio Texas 78209

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 NCT01900249, 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 Oct 2, 2016 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01900249 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →