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QLS-101, 2.0% for Ocular Hypertension

Phase 2
Waitlist Available
Led By Sharon Freedman, M.D.
Research Sponsored by Qlaris Bio, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 28 days
Awards & highlights
No Placebo-Only Group

Summary

This trial tests a new treatment called QLS-101 for adolescents with Sturge-Weber Syndrome who have high eye pressure. The medicine is applied to both eyes every morning for about a month to help reduce the pressure.

Eligible Conditions
  • Ocular Hypertension
  • Sturge-Weber Syndrome
  • Glaucoma

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~28 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 28 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Ocular safety
Systemic safety
Secondary study objectives
Ocular hypotensive effectiveness

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: QLS-101, 2.0%Experimental Treatment1 Intervention
Qlaris' investigational product, QLS-101, 2.0% concentration, ocular administration (eye drop), given once daily in the morning to both eyes
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
QLS-101 ophthalmic solution, 2.0 %
2022
Completed Phase 2
~10

Find a Location

Who is running the clinical trial?

Qlaris Bio, Inc.Lead Sponsor
6 Previous Clinical Trials
285 Total Patients Enrolled
4 Trials studying Ocular Hypertension
195 Patients Enrolled for Ocular Hypertension
Sharon Freedman, M.D.Principal InvestigatorDuke Eye Center
~1 spots leftby Nov 2025