drugset / Trial / NCT05261386

Safety, Efficacy and Pharmacokinetics of CBT-008 in Patients With Meibomian Gland Dysfunction

NCT05261386 ↗

Phase 2 Completed 95 enrolled Cloudbreak Therapeutics, LLC
RandomizedParallel-groupTriple-blindTreatment

Summary

Study Design Structure: Multicenter, randomized, double-masked, vehicle-controlled, parallel group study Duration: 1 month of TID treatment Treatment Groups, Dosing, and Treatment Regimen Study Treatment: CBT-008 topical ophthalmic solution Control Treatment: CBT-008 vehicle

Timeline

Start
2022-03-04
Primary completion
2022-09-07
Completion
2023-03-29

Drugs

EvaluationDrugModalityDoseRoute
Subject CBT-008 Unknown — Topical

Indications