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Active (not recruiting) Phase 3 NCT05456425

A Clinical Trial on Safety and Efficacy of CBT-001 in Patients With Pterygium

Phase 3 – large-scale trial before approval
Conditions: Pterygium

Sponsor: Cloudbreak Therapeutics, LLC

trial.available_in: БГ
Overview
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.
Description
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.
Who can participate
Inclusion Criteria: Pterygium with conjunctival hyperemia Exclusion Criteria: Pterygium removal within the last 6 months
Locations 5
Australia (1)
The Centre for Eye Research Australia
East Melbourne , Melbourne
China (1)
Beijing Tongren Hospital; CMU
Beijing
India (1)
Advanced Eye Centre PGIMER
Chandigarh , Chandigarh
New Zealand (1)
Auckland Eye
Auckland
United States (1)
Trinity Research Group
Dothan , Alabama
Technical details
Status
Active (not recruiting)
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
12 Years
Healthy volunteers
No
Start date
30.06.2022
Completion date
31.12.2027
Registry ID
NCT05456425
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.