The Hydrus™ Microstent
Expanding MIGS
Treatment Opportunities
• $132 MM raised to date
from multinational VC
base
• Over 3,200 patients
treated globally (21
countries, 80 surgeons)
• Studied in multiple level-
one clinical studies and
a large global registry
Global Hydrus Procedures
Ivantis Overview
Investigational Device Only in US 2
MISSION
Expand patient treatment and improve outcomes
through an innovative MIGS solution
SAFETY
20%
Investigational Device Only in US
MIGS Treatment Paradigm
1) “The Emergence of the 5-Tool Glaucoma Surgeon”, AGS 2017
MILD / MODERATE LATE MODERATE / ADVANCED
80%
5M US Diagnosed Glaucoma Patients
CONVENTIONAL OUTFLOW
Schlemm’s Canal
iStent
BYPASS DEVICES
Suprachoroidal/ Subjunctival
InnFocusCyPassXEN
“Canal Will Be First.”
- Thomas Samuelson, MD1
Comprehensive Ophthalmologist Glaucoma Specialist
~$1.6B3
$300M2
$240M2
$225M2
2) Bypass device valuations reflect upfront acquisition price and do not include milestone payments
3) GKOS Public Market Valuation as of May 1, 2017
Hydrus: Next Generation Canal-based MIGS
Investigational Device Only in US
Tri-Modal Mechanism of Action
DILATION COVERAGE
90º
Optimal
Outflow
BYPASS
Reliable Access to Multiple Collector Channels
Leads to Consistent Results
Investigational Device Only in US 5
STANDALONE
(glaucoma only)
COMBINED
(phaco/glaucoma)
Hydrus Expands Treatment Opportunities
Investigational Device Only in US
Hydrus Addresses Treatment Needs in
Both Markets
T R E AT M E N T R E S P O N S E
80%
46%
0%
20%
40%
60%
80%
100%
24 Months
20% Drop in Washed Out
Diurnal IOP
Hydrus
Control
Analysis conducted on intention-to-treat basis
(N=50) (N=50)
(N=50) (N=50)
Superior Outcomes in Combined Procedure
Investigational Device Only in US 7
= 34%
P = 0.0008
Hydrus increases
response by 74%
558 Subject HORIZON
U.S. Pivotal 2 year data
will be presented at AAO
2017
Value Proposition for Comprehensive
Ophthalmologist and Referring Optometrist
Investigational Device Only in US
• “One and done” and
reproducible approach
• Allows for access to
multiple collector
channels every time
RELIABLE
PLACEMENT
HIGHEST PATIENT
SATISFACTION
• Surgeon “promise” is
optimal refractive
outcome with best chance
to be safely off
medications
STANDALONE
(glaucoma only)
COMBINED
(phaco/glaucoma)
Hydrus Expands Treatment Opportunities
Investigational Device Only in US
Hydrus Addresses Treatment Needs in
Both Markets
Investigational Device Only in US
Standalone: The Next Frontier in MIGS
MILD MODERATE ADVANCED
COMPARE
Landmark Comparative Effectiveness Trial
• First level-one MIGS trial comparing 2 MIGS
devices in prospective, controlled conditions
• Mild to moderate glaucoma
• 152 eyes, 11 centers, 8 countries
• Expert users (performed at least 20 of each
procedure prior to trial)
• Full 1 year results collected and now collecting
2 year results
• Trial announced last week
• Advanced (Refractory Glaucoma)
• 60 patients, 15 centers, US and ex-US, with
12 month follow-up
• First patient projected within 30 days
• First MIGS device to have 2 FDA pivotal trials on
opposite ends of glaucoma disease spectrum
SUMMIT
Refractory Glaucoma IDE Trial
• Evaluation of “real-world” Hydrus Microstent utilization, safety, and
effectiveness
• Full spectrum of glaucoma, from mild-moderate to refractory
• 28% of procedures stand-alone
• > 2,000 eyes at 45 centers in 14 countries
SPECTRUM
Global Multi-center Registry
• Micro pressure sensor housed within
Hydrus
• Wireless link to a smart phone
Investigational Device Only in US 11
Unique Design Allows for Platform Technology
24 Hour IOP Monitor
ADVANCED
DISEASE
• Hydrus platform to provide long-term
drug delivery
• Delivery of therapeutic agent that works
with Hydrus to enhance both MOAs
Bioresorbable Drug Delivery
Expanded Indications
• Potential applications in other markets
such as angle closure glaucoma and
normal tension glaucoma
NEW
MARKETS
DIAGNOSTIC

Ophthalmology Innovation Showcase 1 - Ivantis

  • 1.
    The Hydrus™ Microstent ExpandingMIGS Treatment Opportunities
  • 2.
    • $132 MMraised to date from multinational VC base • Over 3,200 patients treated globally (21 countries, 80 surgeons) • Studied in multiple level- one clinical studies and a large global registry Global Hydrus Procedures Ivantis Overview Investigational Device Only in US 2 MISSION Expand patient treatment and improve outcomes through an innovative MIGS solution
  • 3.
    SAFETY 20% Investigational Device Onlyin US MIGS Treatment Paradigm 1) “The Emergence of the 5-Tool Glaucoma Surgeon”, AGS 2017 MILD / MODERATE LATE MODERATE / ADVANCED 80% 5M US Diagnosed Glaucoma Patients CONVENTIONAL OUTFLOW Schlemm’s Canal iStent BYPASS DEVICES Suprachoroidal/ Subjunctival InnFocusCyPassXEN “Canal Will Be First.” - Thomas Samuelson, MD1 Comprehensive Ophthalmologist Glaucoma Specialist ~$1.6B3 $300M2 $240M2 $225M2 2) Bypass device valuations reflect upfront acquisition price and do not include milestone payments 3) GKOS Public Market Valuation as of May 1, 2017
  • 4.
    Hydrus: Next GenerationCanal-based MIGS Investigational Device Only in US Tri-Modal Mechanism of Action DILATION COVERAGE 90º Optimal Outflow BYPASS
  • 5.
    Reliable Access toMultiple Collector Channels Leads to Consistent Results Investigational Device Only in US 5
  • 6.
    STANDALONE (glaucoma only) COMBINED (phaco/glaucoma) Hydrus ExpandsTreatment Opportunities Investigational Device Only in US Hydrus Addresses Treatment Needs in Both Markets
  • 7.
    T R EAT M E N T R E S P O N S E 80% 46% 0% 20% 40% 60% 80% 100% 24 Months 20% Drop in Washed Out Diurnal IOP Hydrus Control Analysis conducted on intention-to-treat basis (N=50) (N=50) (N=50) (N=50) Superior Outcomes in Combined Procedure Investigational Device Only in US 7 = 34% P = 0.0008 Hydrus increases response by 74% 558 Subject HORIZON U.S. Pivotal 2 year data will be presented at AAO 2017
  • 8.
    Value Proposition forComprehensive Ophthalmologist and Referring Optometrist Investigational Device Only in US • “One and done” and reproducible approach • Allows for access to multiple collector channels every time RELIABLE PLACEMENT HIGHEST PATIENT SATISFACTION • Surgeon “promise” is optimal refractive outcome with best chance to be safely off medications
  • 9.
    STANDALONE (glaucoma only) COMBINED (phaco/glaucoma) Hydrus ExpandsTreatment Opportunities Investigational Device Only in US Hydrus Addresses Treatment Needs in Both Markets
  • 10.
    Investigational Device Onlyin US Standalone: The Next Frontier in MIGS MILD MODERATE ADVANCED COMPARE Landmark Comparative Effectiveness Trial • First level-one MIGS trial comparing 2 MIGS devices in prospective, controlled conditions • Mild to moderate glaucoma • 152 eyes, 11 centers, 8 countries • Expert users (performed at least 20 of each procedure prior to trial) • Full 1 year results collected and now collecting 2 year results • Trial announced last week • Advanced (Refractory Glaucoma) • 60 patients, 15 centers, US and ex-US, with 12 month follow-up • First patient projected within 30 days • First MIGS device to have 2 FDA pivotal trials on opposite ends of glaucoma disease spectrum SUMMIT Refractory Glaucoma IDE Trial • Evaluation of “real-world” Hydrus Microstent utilization, safety, and effectiveness • Full spectrum of glaucoma, from mild-moderate to refractory • 28% of procedures stand-alone • > 2,000 eyes at 45 centers in 14 countries SPECTRUM Global Multi-center Registry
  • 11.
    • Micro pressuresensor housed within Hydrus • Wireless link to a smart phone Investigational Device Only in US 11 Unique Design Allows for Platform Technology 24 Hour IOP Monitor ADVANCED DISEASE • Hydrus platform to provide long-term drug delivery • Delivery of therapeutic agent that works with Hydrus to enhance both MOAs Bioresorbable Drug Delivery Expanded Indications • Potential applications in other markets such as angle closure glaucoma and normal tension glaucoma NEW MARKETS DIAGNOSTIC