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Aposense
Company Presentation
October, 2010
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FORWARD LOOKING STATEMENTS
The following slides contain forward-looking statements that include, but are not limited to, projections about our
business and our future revenues, expenses and profitability. Forward-looking statements involve known and
unknown risks, uncertainties and other factors which may cause the actual events, results, performance,
circumstances or achievements of the Company to be materially different from those expressed or implied by such
forward-looking statements due to factors that include, but are not limited to: (1) our ability to develop and bring to
market new products, (2) our ability to successfully complete any necessary or required clinical studies with our
products, (3) our ability to receive regulatory clearance or approval to market our products or changes in regulatory
environment, (4) our success in implementing our sales, marketing and manufacturing plans, (5) the level of adoption
of our products by medical practitioners, (6) the emergence of other products that may make our products obsolete,
(7) protection and validity of patents and other intellectual property rights, (8) the effect of competition by other
companies and technologies, and (9) our ability to obtain reimbursement for our products from government and
commercial payers. You are cautioned not to place undue reliance on these forward-looking statements, which speak
only as of the date of this slides. The Company undertakes no obligation to update any forward-looking statements,
to report events or to report the occurrence of unanticipated events that may lead to the actual events, results,
performance, circumstances or achievements of the Company being different than as envisaged by such forward
looking statements.
ApoptosisProgrammed Cell Death
Aposense®
Targeted Therapies
2010
2011
Oncology program with
TEVA
Lead compound (ATT-11T)
in pre-clinical POC studies
ATT-11T towards IND
New oncology candidates
New Therapeutic Areas
Molecular
Imaging
2010
2011
2 Phase II studies
IBA Strategic partnership
GSK clinical collaboration
Complete one phase II
Prepare for phase III
Expand to other cancers
Aposense®
Targeting Molecules
Forward-Looking Information Notice: The Company’s estimates regarding the above mentioned milestones for the year 2011
depend, among other things, on successful results from pre-clinical and clinical experiments, regulatory approvals and patient
recruitment rate, and other risk factors described in the company’s prospectus.
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InfectiousGenetic
Ischemic
Metabolic
Inflammatory
Other
There is a biological process involved in almost every disease…
CellApoptosisProgrammed Cell Death
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The “black box” of treating cancer
Proposed solution: visualizing treatment effect by imaging of apoptosis
Pre-treatment MRI 2-months post
treatment MRI2
2-3 months
Diagnosis Treatment Follow-up
Average efficacy of chemotherapy 25%1
1 Spear et al., Clinical applications of pharmacogenetics, TRENDS in Molecular Medicine, Vol. 7, No. 5 May 2001
2 Metastatic brain tumor treated with radiation
57% tumor shrinkage“Partial Response”
18% tumor shrinkage“Non-responder”
Modify treatment
Switch treatment
Stop Treatment
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Multi-$Bn Addressable Market
* The Frankel Group, 2002
Cancer patients diagnosed & treated w/
chemo/radiation as first-line treatmentU.S., EU, JP
1,300,000
Average scans 4/patient(2/treatment X 2 treatments/patient)
5,200,000
Addressable Market for EarliTest™Assuming $700/scan
$3.6 Bn
$60Bn
Annual spend on cancer drugs: $80Bn
Average effectiveness: 25%
Spear et al., Clinical applications of pharmacogenetics, TRENDS in Molecular Medicine, Vol. 7, No. 5 May 2001
$20Bn
Pharma Clinical Collaborations
Clinical Use
Phase 2a
2011
FDA
EMEAPhase 2b Phase 3Phase 1
Pharma
companies new
cancer drug
trialsPharma 2
Pharma 3
• Access to clinical data
• Lowering overall costs
• Expediting approval venue
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Global Strategic Collaboration for
Commercialization of EarliTest (ML-10)
2010
2011
GMP implementation
North-East US, France
Expand coverage
Prepare to phase III
Labeling & Distribution Joint
Marketing
Activities
Radio-Labeling, Distribution,Marketing
Strategic Agreement with IBA
Largest Global Distribution Network
• IBA responsible for global labeling and distribution, at its cost
• Revenue share 50/50
• IBA to participate in half of the costs of phase 3, future trials and marketing
Forward-Looking Information Notice: The Company’s estimates regarding the above mentioned commercialization of the EarliTest
(ML-10) timeline depend, among other things, on successful results from pre-clinical and clinical experiments, regulatory approvals
and patient recruitment rate, and other risk factors described in the company’s prospectus.
ApoptosisProgrammed Cell Death
First
sign of disease
Molecular
ImagingTargeted
Therapies
ATTAposense® Targeted Therapy
Aposense®
Targeting Molecules
• Apoptosis: a target for multiple diseases
• Delivering a known drug / API
• Every Aposense®-drug conjugate is a new molecule
Aposense® Targeted Therapy (ATT)
Known DrugAposense®
New Targeted Drug
TUMORTUMOR
ATT Oncology
Chemo
Hypothesized mechanism
Aposense® moleculeAposense®
0
500
1000
1500
2000
2500
3000
3500
4000
10 15 20 25 30 35 40 45 50 55 60
Tumor size (mm3)
Days from
tumor
inoculation
Human
melanoma
implanted in mice
ATT-11T in MelanomaCo-development with
Tx
End
Non-Treated(Control group)
ATT-11T45mg/k (5X9)
Irinotecan225mg/k (75X3)
• Camptosar® (Pfizer)
• >$1Bn annual sales
before becoming generic
(2008/9)
IrinotecanAposense®
ATT-11T
Tumor Free Survival
ATT-11TIrinotecan
40%0%(60 days post treatment)
* No adverse
reactions
observed
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Non-Treated Tumor treated with ATT-11T
Pre-Clinical
ATT-11T in MelanomaCo-development with
ATT-11T in ovarian carcinomaCo-development with
0
100
200
300
400
500
600
700
800
900
1000
1100
1200
1 3 5 7 9 11 13 15 17 19 21 23 25 27 29 31 33 35 37 39 41 43 45 47 49
Non-Treated(Control group)
Irinotecan3X18 mg/k
ATT-11T3X20 mg/k
Tx
End
Days post treatment
Tumor volume (mm3)
Ovarian
cancer
model
Aposense Targeted Therapy (ATT):
Building an Exciting Pipeline
ONCOLOGY
• ATT-11T: Promising results
• Significant advantage over
irinotecan
• TEVA to invest up to additional $9M
• Aposense to choose economic
share 7%-50%
• Goal: Submit IND in 2011
• Develop new compounds
NEW THERAPEUTIC AREAS
2011
Forward-Looking Information Notice: The Company’s estimates regarding the above mentioned targets, milestones and pipeline for the
year 2011 depend, among other things, on successful results from pre-clinical and clinical experiments, regulatory approvals and patient
recruitment rate, successful collaboration with its strategic partners and other risk factors described in the company’s prospectus.
Aposense®
Targeted Therapies
2010
2011
Oncology program with
TEVA
Lead compound (ATT-11T)
in pre-clinical POC studies
ATT-11T towards IND
New oncology candidates
New Therapeutic Areas
Molecular
Imaging
2010
2011
2 Phase II studies
IBA Strategic partnership
GSK clinical collaboration
Complete one phase II
Prepare for phase III
Expand to other cancers
ApoptosisProgrammed Cell Death
Aposense®
Targeting Molecules
Shareholders
Industry Teva Pharmaceuticals
J&J
Venture Capital(life Science)
Pontifax
Ziegler-MediTech
Clal Biotechnology
Docor (Van Leer Foundation)
Bargal (Petrochemicals)
Federman Holdings
Technorov
Investment companies
Bank Leumi
Phoenix Insurance Corp.
JP Morgan
Hachshara Insurance Corp.
Financial
Institutions
Board of Directors
Eli Hurvitz, ChairmanFormer CEO and Chairman
TEVA Pharmaceuticals
Ilan Ziv, MD, Vice-Chairman & CTO
Neurologist, Aposense Founder
Jacob GottensteinChairman of Israeli Petrochemical Industries
Aposense Co-Founder
Morry Blumenfeld, PhDPartner, Ziegler-MediTech Partners
Formerly Chief Scientist, GE Healthcare
Alon Dumanis, PhDCEO of Docor, of the Van Leer Foundation
Ret. General, IAF
Amos Bar-ShalevTechnorov
Jospeh Dobrovsky, PhDFormerly head of drug procurement, Clalit HMO
Anat Shirvan, PhDFounder and former VP R&D, Aposense
Shirith Kasher, Adv.Head of Corporate & Structured Finance, BCRE
Shay Brill, MDDirector General, Beit Rivka Geriatric Center
Management
Yoram AsheryChief Executive Officer
Formerly VP Business Development,
Given Imaging
Eli Frydman, PhDChief Operations Officer
Formerly Business Development Manager,
GE Healthcare
Miri Ben-Ami, MDVP Clinical and Reg. Affairs
Formerly Head Neuro/CNS Therapeutic
Area, Innovative R&D,
TEVA Pharmaceuticals
Dovi Farkash, CPA, Adv.Chief Financial Officer
Formerly VP Finance, M-Systems
Menashe Levi, PhDVP Research & Early Development
Formerly VP R&D Colbar, VP R&D and Co-
Founder Gamida-Cell, CTO Rostam
Business & Scientific Leadership
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2011 Major Milestones
• Molecular Imaging
– EarliTest (ML-10) Complete phase II in one indication
– Initiate phase III preparations
– Expand program: other cancers and beyond oncology
– Expand collaborations with major pharma
– Expand IBA distribution coverage
• Targeted Therapy
– Oncology
ATT-11T toward IND
New compounds
– New Therapeutic Areas
Forward-Looking Information Notice: The Company’s estimates regarding the above mentioned targets, milestones and pipeline for
the year 2011 depend, among other things, on successful results from pre-clinical and clinical experiments, regulatory approvals and
patient recruitment rate, successful collaboration with its existing and new strategic partners and other risk factors described in the
company’s prospectus.
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Thank you