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10% CBT-006 for Meibomian Gland Dysfunction
Phase 2
Waitlist Available
Research Sponsored by Cloudbreak Therapeutics, LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
Study Summary
STUDY DESIGN Structure: Multicenter, randomized, double-masked, vehicle-controlled, parallel group study. Duration: 3 months of TID treatment. Treatment Groups, Dosing, and Treatment Regimen: Study Treatment: CBT-006 topical ophthalmic solution Control Treatment: CBT-006 vehicle
Eligible Conditions
- Meibomian Gland Dysfunction
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Incidence of treatment-emergent adverse events
Secondary outcome measures
Ocular discomfort score (0-4)
Trial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: 2.5% CBT-006Experimental Treatment1 Intervention
Group II: 10% CBT-006Experimental Treatment1 Intervention
Group III: CBT-006Placebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CBT-006
2021
Completed Phase 2
~90
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Who is running the clinical trial?
Cloudbreak Therapeutics, LLCLead Sponsor
5 Previous Clinical Trials
926 Total Patients Enrolled
1 Trials studying Meibomian Gland Dysfunction
92 Patients Enrolled for Meibomian Gland Dysfunction
Frequently Asked Questions
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