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Multicenter, Double-Masked, Randomized, Vehicle-Controlled 12-Month Parallel Comparison of the Safety and Efficacy of 0.1% and 0.2% CBT-001 Versus Vehicle, Dosed Twice-Daily, in Patients With Pterygium
The objective is to evaluate the safety and efficacy of low dose and high dose CBT-001 eye drop dosed twice daily for 24 months compared to vehicle in reducing conjunctival hyperemia and preventing pterygium progression in eyes with pterygia.
Clinical Hypotheses: 1. CBT-001 dosed twice daily is more effective than vehicle in: * Reducing conjunctival hyperemia by demonstrating a statistically significant difference and clinically relevant improvement in the mean severity grade change from baseline. * Preventing pterygium progression, by demonstrating a statistically significant and clinically relevant improvement on drug vs vehicle mean difference in the change in pterygium length from baseline. 2. CBT-001 dosed twice daily maintains the above efficacies and has an acceptable ocular and systemic safety and tolerability profile when administered topically.
Age
12 - No limit years
Sex
ALL
Healthy Volunteers
No
Trinity Research Group
Dothan, Alabama, United States
Horizon Eye Specialists & LASIK Center
Sun City, Arizona, United States
West Coast Eye Institute
Bakersfield, California, United States
Global Research Mangement
Glendale, California, United States
Inland Eye Specialists
Hemet, California, United States
Eye Research Foundation
Newport Beach, California, United States
Shultz Chang Vision
Northridge, California, United States
North Bay Eye Associates INC
Petaluma, California, United States
Santa Barbara Eye Care
Santa Barbara, California, United States
Advanced Research; LLC
Deerfield Beach, Florida, United States
Start Date
June 30, 2022
Primary Completion Date
December 31, 2026
Completion Date
December 31, 2027
Last Updated
September 24, 2025
660
ACTUAL participants
CBT-001
DRUG
Vehicle
DRUG
Lead Sponsor
Cloudbreak Therapeutics, LLC
NCT07244276
NCT07458126
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04683159