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A Study to Determine the Safety and Tolerability of 2 Concentrations of QLS-101

Glaucoma Clinical Trial

Official title:
Masked, Randomized, Single-site, Crossover Study to Determine the Safety and Tolerability of 2 Concentrations of QLS-101 Dosed for 14 Days in Adult Subjects With Sturge-Weber Syndrome (SWS)-Related Glaucoma Due to Elevated Episcleral Venous Pressure (EVP)

Clinical Trial Summary

Safety and tolerability study of 2 concentrations of QLS-101 for adult subjects with Sturge Weber Syndrome (SWS)-related glaucoma due to elevated episcleral venous pressure (EVP).

Clinical Trial Description

Masked, randomized, single site, crossover study to compare 2 concentrations of QLS-101. Subjects will be randomized to one of 2 concentrations of QLS-101 for the first 14 days of daily dosing, and after a 14-day washout period they will be crossed over to the other concentration for another 14 days of daily dosing. Dose assignment is masked to patient and investigator. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04947124
Study type Interventional
Source Qlaris Bio, Inc.
Contact
Status Completed
Phase Phase 2
Start date October 19, 2021
Completion date August 1, 2022
View Details
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