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CBT-001 Eye Drops for Pterygium

Phase 3
Recruiting
Led By Bruce A Segal, ND
Research Sponsored by Cloudbreak Therapeutics, LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 month
Awards & highlights
Pivotal Trial

Summary

This trial is testing CBT-001 eye drops to see if they can reduce eye redness and stop tissue growth in people with pterygia. The drops are used regularly over an extended period. The goal is to find out if these drops work effectively and are safe to use.

Who is the study for?
This trial is for individuals at least 12 years old with pterygium and good general health. They must have a visual acuity of 20/200 or better in one eye, agree to use contraception if applicable, and not be pregnant or nursing. Excluded are those with uncontrolled diseases like cancer, active ocular infections, significant corneal abnormalities unrelated to pterygium, recent eye surgeries (except for pterygium excision), severe seasonal ocular allergies, history of ocular herpes or trauma.
What is being tested?
The trial tests the safety and effectiveness of CBT-001 emulsion at two different concentrations (0.1% and 0.2%) against a placebo vehicle. Participants will apply the treatment twice daily for two years to see if it reduces redness and prevents the growth of their pterygium.
What are the potential side effects?
While specific side effects aren't listed here, participants may experience reactions related to eye treatments such as irritation, discomfort, redness or allergic responses due to sensitivity towards components in CBT-001.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 month
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 month for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
conjunctival hyperemia
pterygium length

Awards & Highlights

Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

3Treatment groups
Experimental Treatment
Placebo Group
Group I: CBT-001 Low DoseExperimental Treatment1 Intervention
CBT-001 eye drop
Group II: CBT-001 High DoseExperimental Treatment1 Intervention
CBT-001 eye drop
Group III: VehiclePlacebo Group1 Intervention
Emulsion eye drop without drug

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Pterygium, such as anti-inflammatory and anti-angiogenic therapies, work by targeting the underlying processes that contribute to the growth and progression of the condition. Anti-inflammatory treatments reduce inflammation in the conjunctiva, which can help alleviate symptoms like redness and irritation. Anti-angiogenic treatments inhibit the formation of new blood vessels, which is crucial because excessive vascularization can lead to the growth and recurrence of Pterygium. These mechanisms are important for Pterygium patients as they address both the symptoms and the root causes of the condition, potentially reducing the need for surgical intervention and improving overall eye health.

Find a Location

Who is running the clinical trial?

Cloudbreak Therapeutics, LLCLead Sponsor
5 Previous Clinical Trials
421 Total Patients Enrolled
1 Trials studying Pterygium
75 Patients Enrolled for Pterygium
Bruce A Segal, NDPrincipal InvestigatorBruce A. Segal, MD

Media Library

CBT-001 (Other) Clinical Trial Eligibility Overview. Trial Name: NCT05456425 — Phase 3
Pterygium Research Study Groups: CBT-001 Low Dose, CBT-001 High Dose, Vehicle
Pterygium Clinical Trial 2023: CBT-001 Highlights & Side Effects. Trial Name: NCT05456425 — Phase 3
CBT-001 (Other) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05456425 — Phase 3
~186 spots leftby Dec 2025