Investor Presentaiton
Program of Data Collection Continuing
ریع
Clinical Study Program - additional data collation de-risks exposure to future reimbursement changes
Study Name
Study Type
Study Sites
Study Details
iTrack TM Global
Data Registry
WCG IRB (approval
number) 20200728
Prospective,
multicenter,
real-world
registry study
20+ sites in the
USA, UK, Canada,
Australia, Singapore
and Germany.
•
•
350+ patient data entries
completed since mid 2022
All glaucoma severities i.e.,
mild, moderate and severe
Study Synopsis
•
Independent cloud-based platform that collates efficacy and
safety data for the canaloplasty procedure (iTrack TM and
iTrack TM Advance)
Hosted in collaboration with the International Glaucoma
Surgery Registry (IGSR), the official registry partner of the
European Glaucoma Society (EGS).
Prospective,
multicenter
randomised control
CATALYST
Study
NCT05564091
trial.
MAGIC
Study (Europe)
NCT05786196
5+ sites in Germany,
•
140 patients in total
(recruitment ongoing)
Mild-moderate glaucoma
Canaloplasty performed in
combination with cataract
surgery
"Cataract Surgery in Conjunction with Canaloplasty via an Ab-
Interno Approach in Patients with Mild to Moderate Primary
Open-Angle Glaucoma"
Comparison of iTrack TM Advance performed in combination
with cataract surgery, compared to cataract surgery alone.
.
the Netherlands and
Australia
Prospective,
multicenter
randomised control
trial.
5+ sites in the UK,
Italy, Spain and
Germany.
•
78 patients in total (recruitment
ongoing)
• Mild-moderate glaucoma
•
Canaloplasty performed as a
standalone procedure
Multicenter Glaucoma Study Investigating Standalone
Canaloplasty
Comparison of the iTrack TM Advance as compared to the
OMNIⓇ Surgical System (Sight Sciences).
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