The technology to conquer glaucoma
Chris Pulling
CEO
cpulling@microoptx.com
BG Implant Overview
 Novel nanotechnology implant that shunts aqueous directly to the
tear film without risk of internal infection
 >$1MM already invested by principals; >$3.4MM total
 Just closing $2.2MM series B
 Funding through 10 patient US feasibility trial
 Successful prototype development with foundational bench and
animal data
 Proven, expert and hands-on leadership team
 Clear and achievable regulatory AND reimbursement path
Glaucoma
 Common : 105 million WW, doubling in 20 years
 Devastating : second leading cause of blindness
in the world (cataracts)
 Leading cause of irreversible blindness
 polls show shorter life preferred over
blindness
 Unmet Need : no treatment universally accepted
as safe and effective; WHO has dropped
glaucoma screening
The Brown Glaucoma Implant
 Shunts directly to the tear film
 No bleb
 Not shunting to enclosed space within eye; scarring/plugging is not a failure mode
 No episcleral venous pressure component => resorption, nocturnal supine IOP
increase
 Has a filter providing precise flow control (P=RxF)
 Filter is the only source of resistance to AH outflow
 Engineered to achieve 8-12mmHg IOP
 Surface biocompatibility good; hydration shell in inner lumen resists
attachments of proteins, cells, and bacteria
 Bulk biocompatibility good. Rigidity match with sclera + surface
biointegration = no micromotion
 Three issued patents; two provisionals filed
Dime
BG Implant
Current Technology
Dime
Collagen Type 1
Collagen Type 1
Structural Polymer
Polyethylene Glycol (low MW)
Polyethylene Glycol (high MW)
Polyethylene Glycol (low MW)
Polyethylene Glycol (high MW)
Structural Polymer
AH Outflow
Filter
Nanofabrication / micromachining
P=FxR
(PEG)
Self-
priming
Lumen’s PEG surface:
Very hydrophilic
(bacterial broth)
Pressure in 2-Week Flow Test
0 48 96 144 192 240 288 336
0
10
20
30
40
50
PressureDrop(mmHg)
Time (hour)
Flow rate: 2.5 ml/min (physiological)
Complete Bacterial Exclusion after 2-weeks
Outlet Inlet Flow
No bacteria were found
inside the device
BacterialBroth
Initial Animal Safety Testing
 Easily implantable
 Tolerated well
 Securely scarred into place
 No infection, with no PMNs or bacteria seen
within or around the device
 Constant AH bathing of cornea not irritant
 OSD, dry eye
MicroOptx Summary
 Shunts AH directly to the tear film: no bleb; no EVP
component to raise nocturnal IOP
 Hits Threshold IOP, and no hypotony
 Inner lumen PEG: resists bacterial, protein, and cell
adherence
 Biointegrates with sclera, so no tunnel infection risk
 In human trials in 9-12 months
Ending the worlds leading cause of blindness

MicroOptx Medical

  • 1.
    The technology toconquer glaucoma Chris Pulling CEO [email protected]
  • 2.
    BG Implant Overview Novel nanotechnology implant that shunts aqueous directly to the tear film without risk of internal infection  >$1MM already invested by principals; >$3.4MM total  Just closing $2.2MM series B  Funding through 10 patient US feasibility trial  Successful prototype development with foundational bench and animal data  Proven, expert and hands-on leadership team  Clear and achievable regulatory AND reimbursement path
  • 3.
    Glaucoma  Common :105 million WW, doubling in 20 years  Devastating : second leading cause of blindness in the world (cataracts)  Leading cause of irreversible blindness  polls show shorter life preferred over blindness  Unmet Need : no treatment universally accepted as safe and effective; WHO has dropped glaucoma screening
  • 4.
    The Brown GlaucomaImplant  Shunts directly to the tear film  No bleb  Not shunting to enclosed space within eye; scarring/plugging is not a failure mode  No episcleral venous pressure component => resorption, nocturnal supine IOP increase  Has a filter providing precise flow control (P=RxF)  Filter is the only source of resistance to AH outflow  Engineered to achieve 8-12mmHg IOP  Surface biocompatibility good; hydration shell in inner lumen resists attachments of proteins, cells, and bacteria  Bulk biocompatibility good. Rigidity match with sclera + surface biointegration = no micromotion  Three issued patents; two provisionals filed
  • 5.
  • 6.
    Collagen Type 1 CollagenType 1 Structural Polymer Polyethylene Glycol (low MW) Polyethylene Glycol (high MW) Polyethylene Glycol (low MW) Polyethylene Glycol (high MW) Structural Polymer AH Outflow Filter Nanofabrication / micromachining P=FxR (PEG)
  • 7.
  • 8.
  • 9.
    Pressure in 2-WeekFlow Test 0 48 96 144 192 240 288 336 0 10 20 30 40 50 PressureDrop(mmHg) Time (hour) Flow rate: 2.5 ml/min (physiological)
  • 10.
    Complete Bacterial Exclusionafter 2-weeks Outlet Inlet Flow No bacteria were found inside the device BacterialBroth
  • 11.
    Initial Animal SafetyTesting  Easily implantable  Tolerated well  Securely scarred into place  No infection, with no PMNs or bacteria seen within or around the device  Constant AH bathing of cornea not irritant  OSD, dry eye
  • 12.
    MicroOptx Summary  ShuntsAH directly to the tear film: no bleb; no EVP component to raise nocturnal IOP  Hits Threshold IOP, and no hypotony  Inner lumen PEG: resists bacterial, protein, and cell adherence  Biointegrates with sclera, so no tunnel infection risk  In human trials in 9-12 months
  • 13.
    Ending the worldsleading cause of blindness