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More than just a potential
breakthrough treatment
for many cancers
June 2015
22
Critical Outcome Technologies Inc.
Rapidly developing
targeted therapies to
better meet the needs
of patients
 TSX-V: COT
 OTCQB: COTQF
3
Highlights
1
2
3
COTI-2 – lead program in oncology entering
Phase 1 clinical trial in 2015
CHEMSAS – proprietary drug discovery
engine using machine-based learning
Strong pipeline of opportunities in
oncology and other therapeutic areas
4
COTI-2: a promising advance
 Potential breakthrough
treatment for many cancers
 Effective against many
common cancers with a
p53 gene mutation
 > 50% of all human cancers
have a p53 mutation
(eg. ~ 95% of serous ovarian cancers)
5
COTI-2 background
N
N
N
H
S
N
N
N
 3rd generation
Thiosemicarbazone
 A small molecule
discovered by our
CHEMSAS process
 Engineered for low
toxicity and easily
synthesized in 3 steps
 Demonstrates strong in
vitro and in vivo activity
5
6
COTI-2: first- and best-in-class potential
 Novel p53-dependent mechanism of action
 Orally bio-available and effective at low dose
 Low toxicity in preclinical development
 Opportunity for single agent and combination
therapy
 Strong IP protection in place
7
COTI-2 and tumor volumes
Tumors significantly reduced by COTI-2 in all
treatment groups relative to vehicle control
8
COTI-2 reduces p53 resistant protein levels
 COTI-2 significantly reduces p53 mutant protein levels and
significantly increases wild-type p53 protein levels in TOV-
112D cells likely by inducing a conformational change
•(*) Significant
difference in p53
protein levels
between COTI-2
treated and untreated
cells (control)
Mutant p53 Levels in the
presence/absence of
COTI-2
0
20
40
60
80
100
TOV-112D H460
MeanFluorescenceIntensity(ArbitraryUnits)
Cell Line
Control
COTI-2
*
9
COTI-2: effects on p53 protein levels
 COTI-2 has no significant effect on p53 protein levels in the
H460 cell line, which do not carry the mutant p53 protein
•(*) Significant difference
in p53 protein levels
between COTI-2 treated
and untreated cells
(control)
Wild-type p53 Levels in
the Presence/Absence of
COTI-2
0
20
40
60
80
100
120
TOV-112D H460
MeanFluorescenceIntensity(ArbitraryUnits)
Cell Line
Control
COTI-2
*
10
MD Anderson relationship
10
 Confirmed COTI-2’s novel p53 dependent MOA
 Confirmed selective & potent anti-cancer activity
 Identified effective dosage 60% lower than in prior animal
experiments
11
COTI-2: the pathway to the clinic
 Granted orphan drug status for ovarian cancer by FDA in
June 2014
 Completed final pre-clinical studies
 Signed LOI with MD Anderson for Phase 1 clinical
development
 Grant of Investigational New Drug status in May 2015
 Commence Phase 1 clinical trial in 3rd quarter of calendar
2015
12
COTI-2: next steps
12
Complete Phase 1: 46 patients in
gynecologic cancers
Expand indications and
combination therapies
Phase 2: add value – create
partnerships
1313
 Proprietary, machine
learning (AI) based
drug discovery
platform technology
 Big Data analysis
solutions
Building a robust pipeline with CHEMSAS®
14
Costly failed attempts
occur quickly & cheaply
in computer simulations,
not the ‘wet lab’
Increased probability of
clinical & commercial
success
Database driven
computational
replication of
traditional
‘wet lab’ drug
discovery process
14
Advantages of CHEMSAS®
15
Drugs in our pipeline
Therapy
Library
/Compound
Target CHEMSAS Lead
Selection
Synthesis Preclinical Phase 1
Oncology
COTI-2
AML
Colon
Small Cell Lung Cancer Library
COTI-219
COTI-4
COTI-58
6 other leads
Plus projects for MRSA, Multiple sclerosis, Alzheimer’s, and HIV Integrase Inhibitors
16
Summary
1
2
3
COTI-2 – lead program in oncology entering
Phase 1 clinical trial in 2015
CHEMSAS – proprietary drug discovery
engine using machine-based learning
Strong pipeline of opportunities in
oncology and other therapeutic areas
17
When used anywhere in this presentation, whether oral or written, the words expects, believes,
anticipates, estimates and similar expressions are intended to identify forward-looking
statements. Forward-looking statements may include statements addressing future financial and
operating results of Critical Outcome Technologies Inc. (COTI).
COTI bases these forward-looking statements on its current expectations about future events.
Such statements are subject to risks and uncertainties including, but not limited to, the
successful implementation of COTI’s strategic plans, the acceptance of new products, the
obsolescence of existing products, the resolution of potential patent issues, competition,
changes in economic conditions, and other risks described in COTI’s public documents such as
press releases and filings with the Toronto Stock Exchange and the Ontario Securities
Commission.
All forward-looking statements are qualified in their entirety by the cautionary statements
included in this document and such filings. These risks and uncertainties could cause actual
results to differ materially from results expressed or implied by forward-looking statements
contained in this presentation. These forward-looking statements speak only as of the date of
this presentation.
Disclaimer
Follow CriticalOutcome on Twitter,
Facebook, YouTube and SlideShare

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More than just a potential BREAKTHROUGH treatment for many cancers

  • 1. More than just a potential breakthrough treatment for many cancers June 2015
  • 2. 22 Critical Outcome Technologies Inc. Rapidly developing targeted therapies to better meet the needs of patients  TSX-V: COT  OTCQB: COTQF
  • 3. 3 Highlights 1 2 3 COTI-2 – lead program in oncology entering Phase 1 clinical trial in 2015 CHEMSAS – proprietary drug discovery engine using machine-based learning Strong pipeline of opportunities in oncology and other therapeutic areas
  • 4. 4 COTI-2: a promising advance  Potential breakthrough treatment for many cancers  Effective against many common cancers with a p53 gene mutation  > 50% of all human cancers have a p53 mutation (eg. ~ 95% of serous ovarian cancers)
  • 5. 5 COTI-2 background N N N H S N N N  3rd generation Thiosemicarbazone  A small molecule discovered by our CHEMSAS process  Engineered for low toxicity and easily synthesized in 3 steps  Demonstrates strong in vitro and in vivo activity 5
  • 6. 6 COTI-2: first- and best-in-class potential  Novel p53-dependent mechanism of action  Orally bio-available and effective at low dose  Low toxicity in preclinical development  Opportunity for single agent and combination therapy  Strong IP protection in place
  • 7. 7 COTI-2 and tumor volumes Tumors significantly reduced by COTI-2 in all treatment groups relative to vehicle control
  • 8. 8 COTI-2 reduces p53 resistant protein levels  COTI-2 significantly reduces p53 mutant protein levels and significantly increases wild-type p53 protein levels in TOV- 112D cells likely by inducing a conformational change •(*) Significant difference in p53 protein levels between COTI-2 treated and untreated cells (control) Mutant p53 Levels in the presence/absence of COTI-2 0 20 40 60 80 100 TOV-112D H460 MeanFluorescenceIntensity(ArbitraryUnits) Cell Line Control COTI-2 *
  • 9. 9 COTI-2: effects on p53 protein levels  COTI-2 has no significant effect on p53 protein levels in the H460 cell line, which do not carry the mutant p53 protein •(*) Significant difference in p53 protein levels between COTI-2 treated and untreated cells (control) Wild-type p53 Levels in the Presence/Absence of COTI-2 0 20 40 60 80 100 120 TOV-112D H460 MeanFluorescenceIntensity(ArbitraryUnits) Cell Line Control COTI-2 *
  • 10. 10 MD Anderson relationship 10  Confirmed COTI-2’s novel p53 dependent MOA  Confirmed selective & potent anti-cancer activity  Identified effective dosage 60% lower than in prior animal experiments
  • 11. 11 COTI-2: the pathway to the clinic  Granted orphan drug status for ovarian cancer by FDA in June 2014  Completed final pre-clinical studies  Signed LOI with MD Anderson for Phase 1 clinical development  Grant of Investigational New Drug status in May 2015  Commence Phase 1 clinical trial in 3rd quarter of calendar 2015
  • 12. 12 COTI-2: next steps 12 Complete Phase 1: 46 patients in gynecologic cancers Expand indications and combination therapies Phase 2: add value – create partnerships
  • 13. 1313  Proprietary, machine learning (AI) based drug discovery platform technology  Big Data analysis solutions Building a robust pipeline with CHEMSAS®
  • 14. 14 Costly failed attempts occur quickly & cheaply in computer simulations, not the ‘wet lab’ Increased probability of clinical & commercial success Database driven computational replication of traditional ‘wet lab’ drug discovery process 14 Advantages of CHEMSAS®
  • 15. 15 Drugs in our pipeline Therapy Library /Compound Target CHEMSAS Lead Selection Synthesis Preclinical Phase 1 Oncology COTI-2 AML Colon Small Cell Lung Cancer Library COTI-219 COTI-4 COTI-58 6 other leads Plus projects for MRSA, Multiple sclerosis, Alzheimer’s, and HIV Integrase Inhibitors
  • 16. 16 Summary 1 2 3 COTI-2 – lead program in oncology entering Phase 1 clinical trial in 2015 CHEMSAS – proprietary drug discovery engine using machine-based learning Strong pipeline of opportunities in oncology and other therapeutic areas
  • 17. 17 When used anywhere in this presentation, whether oral or written, the words expects, believes, anticipates, estimates and similar expressions are intended to identify forward-looking statements. Forward-looking statements may include statements addressing future financial and operating results of Critical Outcome Technologies Inc. (COTI). COTI bases these forward-looking statements on its current expectations about future events. Such statements are subject to risks and uncertainties including, but not limited to, the successful implementation of COTI’s strategic plans, the acceptance of new products, the obsolescence of existing products, the resolution of potential patent issues, competition, changes in economic conditions, and other risks described in COTI’s public documents such as press releases and filings with the Toronto Stock Exchange and the Ontario Securities Commission. All forward-looking statements are qualified in their entirety by the cautionary statements included in this document and such filings. These risks and uncertainties could cause actual results to differ materially from results expressed or implied by forward-looking statements contained in this presentation. These forward-looking statements speak only as of the date of this presentation. Disclaimer
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