Qlaris Phase 2 clinical study investigating the safety, tolerability, and ocular hypotensive efficacy of QLS-111 in combination with latanoprost in open-angle glaucoma (OAG) and/or ocular hypertension (OHT) patients.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Incidence of ocular treatment-emergent adverse events (TEAEs)
Timeframe: 28 days
Clinically significant change in visual acuity
Timeframe: 28 days
Clinically significant change in findings on slit lamp exam
Timeframe: 28 days
Clinically significant change in findings on fundus exam
Timeframe: 28 days
Incidence of systemic (TEAEs)
Timeframe: 28 days
Clinically significant change in blood pressure
Timeframe: 28 days
Clinically significant change in heart rate
Timeframe: 28 days