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Clinical Trial Summary

The primary purpose of this study is to investigate the safety and efficacy of bilateral DWT in subjects with POAG or OHT compared to active and sham controls. The secondary purpose of the study is to investigate the durability, repeatability, and does response of the same.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02226094
Study type Interventional
Source OcuTherix, Inc.
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date November 2013
Completion date December 2015

See also
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Recruiting NCT06016972 - Qlaris Phase 2 Study of QLS-111 in POAG and/or OHT Patients Phase 2
Completed NCT01318252 - AL-54478 Proof of Concept Study Phase 2
Terminated NCT01180062 - Safety Study of Latanoprost Slow Release Insert Phase 1
Completed NCT01917383 - A Phase II Study to Evaluate the Additivity of Trabodenoson to Latanoprost in Adults With Ocular Hypertension or Primary Open-Angle Glaucoma Phase 2
Completed NCT01670266 - Single and Multiple Dose Escalation and Two-sequence Crossover Study of ONO-9054 in Patients With Ocular Hypertension or Mild Open-angle Glaucoma Phase 1
Completed NCT02829996 - Study of Fixed-Dose Combinations of Trabodenoson and Latanoprost in Adults With OHT or POAG Phase 2
Recruiting NCT06249152 - Qlaris Study of QLS-111 in Combination With a PGA for OAG and/or OHT Patients Phase 2