3 results
Approved WMOCompleted
The purpose of this study is to expand knowledge of the IVANTIS Hydrus Implant's ability to decrease intraocular pressure (the pressure in the eye).
Approved WMOCompleted
Primary:The primary objective of this study is to evaluate the efficacy of LDX administered as a daily morning dose (30, 50, and 70mg/day) compared to placebo over the course of 7 weeks. This study will enrol children and adolescents (6-17 years of…
Approved WMOCompleted
To evaluate the clinical safety and efficacy of the Drug-Coated Balloon Catheter in the treatment of de novo lesions, small vessel disease or ISR with coronary lesions previously treated with drug-eluting or bare metal stents in native coronary…