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www.targovax.com
Arming the patient’s immune system to fight cancer
Redeye - Immunonkologi
September 21st 2017
www.targovax.com
Important notice and disclaimer
This report contains certain forward-looking statements based on uncertainty, since they relate to events and
depend on circumstances that will occur in future and which, by their nature, will have an impact on the results of
operations and the financial condition of Targovax. Such forward-looking statements reflect the current views of
Targovax and are based on the information currently available to the company. Targovax cannot give any assurance
as to the correctness of such statements.
There are a number of factors that could cause actual results and developments to differ materially from those
expressed or implied in these forward-looking statements. These factors include, among other things, risks or
uncertainties associated with the success of future clinical trials; risks relating to personal injury or death in
connection with clinical trials or following commercialization of the company’s products, and liability in connection
therewith; risks relating to the company’s freedom to operate (competitors patents) in respect of the products it
develops; risks of non-approval of patents not yet granted and the company’s ability to adequately protect its
intellectual property and know-how; risks relating to obtaining regulatory approval and other regulatory risks relating
to the development and future commercialization of the company’s products; risks that research and development
will not yield new products that achieve commercial success; risks relating to the company’s ability to successfully
commercialize and gain market acceptance for Targovax’s products; risks relating to the future development of the
pricing environment and/or regulations for pharmaceutical products; risks relating to the company’s ability to secure
additional financing in the future, which may not be available on favorable terms or at all; risks relating to currency
fluctuations; risks associated with technological development, growth management, general economic and
business conditions; risks relating to the company’s ability to retain key personnel; and risks relating to the impact of
competition.
2
www.targovax.com
Agenda
3
Introduction to immunotherapy
ONCOS-102 oncolytic virus platform
TG neo-antigen cancer vaccine platform
Financial highlights
Targovax clinical program overview
www.targovax.com
Immunotherapy has the potential to cure cancer
4
Week 108: complete remission
1 year afterPrior to Yervoy
Real world example – Patient in a Yervoy checkpoint inhibitor trial
IMMUNOTHERAPY
www.targovax.com 5
Response rate to checkpoint inhibitors (CPIs)
Complimentary
immune priming
medicines may make
tumors respond
better to checkpoint
inhibitors
~80%
~84%
~80%
~70%
~70%-80%
~40%
Head and Neck
Lung Carcinoma (NSCLC)
Triple Negative Breast
Renal Cell carcinoma
Bladder
Most patients do not respond to currently available
immunotherapies
Non-respondersResponders
Melanoma
IMMUNOTHERAPY
www.targovax.com
Targovax is developing two drugs to boost the effect of
immunotherapy
6
ONCOS-102
Oncolytic virus
TG01
Neoantigen vaccine
o Cocktail of 7 synthetic peptides acting as
antigens to clinically relevant RAS mutations
o Generates RAS-specific T-cells
o T-cells kill RAS mutated cancer cells
o Genetically tailored Adenovirus
o Selectively infects and lyses cancer cells
o Releases cancer antigens
o Triggers immune response
ONCOS TG
www.targovax.com
Agenda
7
Introduction to immunotherapy
ONCOS-102 oncolytic virus platform
TG neo-antigen cancer vaccine platform
Financial highlights
Targovax clinical program overview
www.targovax.com 8
ONCOS-102 is a cancer targeting adenovirus armed
with an immune stimulating transgene
∆24 bp
Fiber knob
ITRITR
E1A
∆6.7K/gp19K
E3
Transgene
∆Ad5 knob
Ad3 knob
Enhanced
cancer cell
infection
o GM-CSF transgene
o Triggers innate immune response
and recruits APCs
Selective
replication in
cancer cells
Immune system
booster
ONCOS TG
www.targovax.com
Activate immune system:
o Virus injected directly into
the tumor / peritoneum
o Infected cells lyse and
release cancer-specific
antigens
Train T-cells:
o APCs present tumor
specific antigens at lymph
nodes
o Production of tumor
specific T-cells
Attack the cancer:
o Tumor specific T-cells
circulate in the body
o Identify lesions and kill
the cancer cells
Lymph node
9
ONCOS-102 makes tumors visible to the immune system
ONCOS TG
www.targovax.com 10
0,1
1
10
100
1000
10000
FI1-06
FI1-04
FI1-18
FI1-02
FI1-15
FI1-08
FI1-13
FI1-09
FI1-17
FI1-01
FI1-14
FI1-19
5 patients
>8-fold increase
Fold-changefrombaseline
6 patients
up to 5-fold increase
Ranki et al., Journal for Immunotherapy of Cancer 2016, 4(17)
ONCOS TG
Phase I trial data in solid tumors: ONCOS-102 can
make tumors hot
Change in CD8+ T-cell count after treatment with ONCOS-102
www.targovax.com
Targovax has initiated a broad clinical program to test the
clinical benefit of ONCOS-102
11
Initial Phase I trial
Solid tumors
7 indications
o 12 refractory patients
o Monotherapy
o Correlation between
immune activation and
survival
Mesothelioma
Phase I/II - controlled
30 patients
Melanoma
Phase I
12 patients
Prostate
Phase I
10 patients
Ovarian / colorectal
Phase I/II - controlled
78 patients
o Combination with PD-1
CPI in refractory patients
o Proof-of-concept
o Memorial Sloan Kettering
o Combination with chemo
o Randomized controlled trial
o Ultra-orphan indication
o Collaboration with Ludwig & CRI
o Combination with Medimmune’s
durvalumab
o Randomized controlled trial
o Partnered with Sotio
o Combination with DC therapy
ONCOS TG
Compassionate
use program
Finland
115 patients
o Testing within ATAP
EU program
o Individual clinical
responses
o Reassuring safety
data
www.targovax.com
Agenda
12
Introduction to immunotherapy
ONCOS-102 oncolytic virus platform
TG neo-antigen cancer vaccine platform
Financial highlights
Targovax clinical program overview
www.targovax.com
The survival rate for pancreatic cancer patients has
not improved since the 1970s
ONCOS TG
No improvement in
survival over the past 40
years
Improvement in 10 year survival rate
% change over 40yrs. 1972–2012
13
www.targovax.com
The RAS gene is mutated in >85% of pancreatic cancer
patients, making it an interesting therapeutic target
14
One of the most common
mutations in cancer
RAS is a well-defined
neoantigen
Results in cell division
permanently switched on
No existing therapies
targeting RAS
Occurs in >85% of
pancreatic cancer patients
Incidence of RAS mutations
ONCOS TG
100%
50%
0%
www.targovax.com
The TG neoantigen vaccine primes the immune system
to recognize and destroy RAS mutated cancer cells
15
Activate immune system:
o TG vaccine injected
intradermally
o APCs pick up the TG RAS
antigens
Train T-cells:
o APCs present RAS
antigens in lymph node
o Production of RAS
specific T-cells
Attack the cancer:
o RAS specific T-cells
identify cancer cells
displaying mutated RAS
o CD8+ T-cells kill the
cancer cells
Cocktail of 7 peptides
covering all relevant RAS
mutations in pancreas
ONCOS TG
www.targovax.com
The TG vaccine has shown 20% 10 year survival in
earlier Phase I trials in resected pancreatic cancer
16
ONCOS TG
1 Wedén et al., 2011 2 Oettle H et al., JAMA 2007, vol 297, no 3 3 Oettle H et al., JAMA 2013, vol 310, no 14
0
10
20
30
40
50
60
70
80
90
100
0 6 12 18 24 30 36 42 48 54 60 66 72 78 84 90 96 102 108 114 120
o 4/20 (20%) treated patients
alive after 10 years
o 0/87 untreated patients alive
in a similar cohort from the
same period
Survival(%)
Months from resection
10 year survival from historical TG trials in resected pancreatic cancer (monotherapy)
www.targovax.com
These data were corroborated in a recent Phase I/II trial
in combination with modern standard of care
17
Median survival
33.1 months from surgery
27.6 months for SoC (Gemcitabine) in ESPAC-4 study2
Immune
response
18/19 patients (95%) showed TG specific immune activation
Safety
Good safety profile, treatment generally well-tolerated
Some manageable allergic reactions were seen
2 year overall
survival
13 of 19 patients (68%) alive 2 years after surgery
Historical controls 2 year survival range from 30-53%1
1: Relevant historical control trials, not including ESPAC-4, which did not report 2 year OS
2: Based on ESPAC-4 reported 25.5 months median OS from randomisation, adding median time from surgery to randomization of 64 days (2.1 months)
ONCOS TG
Results from TG01-01 trial in resected pancreatic cancer (combination with Gemcitabine)
www.targovax.com
Clinical development overview for TG – Targovax is
seeking potential partnership
18
Phase I/II
Resected
pancreatic cancer
32 patients
o 10 year survival data
o Correlation between
immune response and
survival
o Large safety database
Colorectal
Phase I
20 patients
Resected pancreas
Phase II/III
N=tbd
o TG02, targets 8 mutations
o Combination with Keytruda
o Currently recruiting patients
o 2 arm, controlled trial
o Aimed to reach registration
o Currently seeking partner
ONCOS TG
Phase I
Resected &
non-resected
>200 patients
Historical trials Planned / recruiting trialsCompleting trial
o Encouraging 2 year
survival and median
survival
www.targovax.com
Agenda
Introduction to immunotherapy
ONCOS-102 oncolytic virus platform
TG neo-antigen cancer vaccine platform
Financial highlights
Targovax clinical program overview
19
www.targovax.com
Two platforms and six clinical trials ensures a program
with frequent data readouts
20
Cancer
indication
Combined
with
ONCOS-102
Melanoma CPI
Mesothelioma Chemo* Orphan ind.
Ovarian &
Colorectal
CPI
Orphan ind.
Sponsor: Ludwig
Prostate DC therapy Sponsor: Sotio
TG
Resected
Pancreatic
Chemo* Orphan ind.
Colorectal CPI
4 readouts
2017
5 readouts
2018
2017 2018
H1 H2 H1 H2
2019
H1
Phase l
Phase l/ll
Phase l
Phase lb/ll
Phase I/II
Phase Ib
Interim data Clinical, immune and
safety data
* In combination with Standard of Care Chemoterapy. Pemetrexed/cisplatin for
Mesothelioma and Gemcitabine for Resected Pancreatic
ONCOS TG
Indicative timing of:
www.targovax.com
Agenda
Introduction to immunotherapy
ONCOS-102 oncolytic virus platform
TG neo-antigen cancer vaccine platform
Financial highlights
Targovax clinical program overview
21
www.targovax.com
Targovax has a sound financial position, with cash to
complete the planned clinical program into 2019
Operations
Cash end of Q2 NOK 116m USD 14m June 30st 2017
Net cash flow NOK -32m USD -4m Total Q2
Annual run rate NOK 102m USD 12m Last four quarters
Runway NOK ~300m USD >35m Into 2019
22
The share OSE: TRVX
Market Cap NOK ~1bn USD ~125m At share price NOK ~20
Daily turnover NOK 5m USD 0.6m 6 month avg.
Analysts DNB, ABG Sundal Collier, Arctic, Redeye, Norske Aksjeanalyser
Raised NOK 200 million in private placement June 8 2017
10,000,000 new shares @ NOK 20 per share
CORPORATE
* Including preceeds from raise
www.targovax.com
The shareholder base is strong, with a mix of specialist,
generalist and retail investors
23
CORPORATE
Key international investors participating in PP 2017
– HealthCap (SWE)
– Nyenburgh (NL)
– Trium (UK)
– Millenium Capital Partners (UK)
– Interogo (SWE)
– AP3 (SWE)
– Aramea AM (DE)
Shares and options
▪ 56.4m shares fully diluted
– Average strike price on options ~NOK 21
– Total dilutive effect of options is 6.5%
▪ 52.5m ordinary shares
– Management ownership: 1.7%
– 3,880 shareholders
Shareholder
Shares m Relative
HealthCap Sweden 12,4 23,6 %
Nordea Norway 4,7 8,9 %
RadForsk Norway 4,4 8,4 %
KLP Norway 1,8 3,4 %
Statoil Norway 1,2 2,2 %
Rasmussengruppen Norway 1,0 1,9 %
Danske Bank (nom.) Norway 0,8 1,6 %
Euroclear Bank (nom.) Belgium 0,8 1,4 %
Timmuno Norway 0,7 1,4 %
Prieta AS Norway 0,7 1,4 %
Thorendahl Invest AS Norway 0,7 1,3 %
Sundt AS Norway 0,7 1,2 %
The Bank of NY Mellon (nom.) Belgium 0,3 0,6 %
ABN Amro Global (nom.) Netherland 0,3 0,5 %
Norda ASA Norway 0,3 0,5 %
NHO - P665AK Norway 0,3 0,5 %
Yngve S. Lillesund Norway 0,2 0,4 %
The Bank of NY Mellon (nom.) Belgium 0,2 0,4 %
Tobech Invest AS Norway 0,2 0,4 %
Istvan Molnar Norway 0,2 0,4 %
Top 20 31,8 60,4 %
Other shareholders (3860) 20,8 39,6 %
Total 52,6 100,0 %
Estimated ownership
www.targovax.com
Targovax has an experienced senior management team
in place to execute the development program
CEO - Øystein Soug
o Previously CFO of Algeta ASA
o Track record in bringing an
oncology asset from phase I
through to market launch
o Oversaw the sale of Algeta to
Bayer Healthcare
CMO - Dr. Magnus Jäderberg
o Former CMO of Bristol Myers
Squibb Europe
o Brought Yervoy to market as first-
in-class checkpoint inhibitor
o 25 years of experience in R&D
CFO - Dr. Erik Digman Wiklund
o Former consultant in McKinsey &
Co Pharma practice
o PhD in cancer research
o Various roles in biotech, including
at Algeta ASA
CTO – Jon Amund Eriksen
o Pinoeer in immuno-oncology
o Original inventor of the RAS TG
peptide platform
o 35 years of experience in pharma
R&D and product development
CORPORATE
www.targovax.com
Planned strong news flow with multiple near term
value inflection points
25
2015 2016 2017 2018H1 H2
phase ll initiated
TG01
Immune activation
and MoA demo
ONCOS-102
Interim data
pancreas
TG01 (1st cohort)
Immune activation
pancreas
TG01 (2nd cohort)
2-year survival
pancreas
TG01 (1st cohort)
2-year survival
pancreas
TG01 (2nd cohort)
Initiate phase l/ll
mesothelioma
ONCOS-102
Initiate phase l
prostate
ONCOS-102
Initiate phase l/ll
melanoma
ONCOS-102
Interim data
ovarian /colorectal
ONCOS-102
phase l/ll data
melanoma
ONCOS-102
Interim data
melanoma
ONCOS-102
Interim data
mesothelioma
ONCOS-102
Initiate phase Ib in
colorectal
TG02
Interim data
colorectal
TG02 (mono)
Initiate phase l
Ovarian/colorectal
ONCOS-102
Interim data
prostate
ONCOS-102
phase I data/
colorectal
TG02 (combo)
H1 H2
Listing on OSE main
list
Oslo Stock Exchange
FINANCE

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1709 redeye podium_v2

  • 1. www.targovax.com Arming the patient’s immune system to fight cancer Redeye - Immunonkologi September 21st 2017
  • 2. www.targovax.com Important notice and disclaimer This report contains certain forward-looking statements based on uncertainty, since they relate to events and depend on circumstances that will occur in future and which, by their nature, will have an impact on the results of operations and the financial condition of Targovax. Such forward-looking statements reflect the current views of Targovax and are based on the information currently available to the company. Targovax cannot give any assurance as to the correctness of such statements. There are a number of factors that could cause actual results and developments to differ materially from those expressed or implied in these forward-looking statements. These factors include, among other things, risks or uncertainties associated with the success of future clinical trials; risks relating to personal injury or death in connection with clinical trials or following commercialization of the company’s products, and liability in connection therewith; risks relating to the company’s freedom to operate (competitors patents) in respect of the products it develops; risks of non-approval of patents not yet granted and the company’s ability to adequately protect its intellectual property and know-how; risks relating to obtaining regulatory approval and other regulatory risks relating to the development and future commercialization of the company’s products; risks that research and development will not yield new products that achieve commercial success; risks relating to the company’s ability to successfully commercialize and gain market acceptance for Targovax’s products; risks relating to the future development of the pricing environment and/or regulations for pharmaceutical products; risks relating to the company’s ability to secure additional financing in the future, which may not be available on favorable terms or at all; risks relating to currency fluctuations; risks associated with technological development, growth management, general economic and business conditions; risks relating to the company’s ability to retain key personnel; and risks relating to the impact of competition. 2
  • 3. www.targovax.com Agenda 3 Introduction to immunotherapy ONCOS-102 oncolytic virus platform TG neo-antigen cancer vaccine platform Financial highlights Targovax clinical program overview
  • 4. www.targovax.com Immunotherapy has the potential to cure cancer 4 Week 108: complete remission 1 year afterPrior to Yervoy Real world example – Patient in a Yervoy checkpoint inhibitor trial IMMUNOTHERAPY
  • 5. www.targovax.com 5 Response rate to checkpoint inhibitors (CPIs) Complimentary immune priming medicines may make tumors respond better to checkpoint inhibitors ~80% ~84% ~80% ~70% ~70%-80% ~40% Head and Neck Lung Carcinoma (NSCLC) Triple Negative Breast Renal Cell carcinoma Bladder Most patients do not respond to currently available immunotherapies Non-respondersResponders Melanoma IMMUNOTHERAPY
  • 6. www.targovax.com Targovax is developing two drugs to boost the effect of immunotherapy 6 ONCOS-102 Oncolytic virus TG01 Neoantigen vaccine o Cocktail of 7 synthetic peptides acting as antigens to clinically relevant RAS mutations o Generates RAS-specific T-cells o T-cells kill RAS mutated cancer cells o Genetically tailored Adenovirus o Selectively infects and lyses cancer cells o Releases cancer antigens o Triggers immune response ONCOS TG
  • 7. www.targovax.com Agenda 7 Introduction to immunotherapy ONCOS-102 oncolytic virus platform TG neo-antigen cancer vaccine platform Financial highlights Targovax clinical program overview
  • 8. www.targovax.com 8 ONCOS-102 is a cancer targeting adenovirus armed with an immune stimulating transgene ∆24 bp Fiber knob ITRITR E1A ∆6.7K/gp19K E3 Transgene ∆Ad5 knob Ad3 knob Enhanced cancer cell infection o GM-CSF transgene o Triggers innate immune response and recruits APCs Selective replication in cancer cells Immune system booster ONCOS TG
  • 9. www.targovax.com Activate immune system: o Virus injected directly into the tumor / peritoneum o Infected cells lyse and release cancer-specific antigens Train T-cells: o APCs present tumor specific antigens at lymph nodes o Production of tumor specific T-cells Attack the cancer: o Tumor specific T-cells circulate in the body o Identify lesions and kill the cancer cells Lymph node 9 ONCOS-102 makes tumors visible to the immune system ONCOS TG
  • 10. www.targovax.com 10 0,1 1 10 100 1000 10000 FI1-06 FI1-04 FI1-18 FI1-02 FI1-15 FI1-08 FI1-13 FI1-09 FI1-17 FI1-01 FI1-14 FI1-19 5 patients >8-fold increase Fold-changefrombaseline 6 patients up to 5-fold increase Ranki et al., Journal for Immunotherapy of Cancer 2016, 4(17) ONCOS TG Phase I trial data in solid tumors: ONCOS-102 can make tumors hot Change in CD8+ T-cell count after treatment with ONCOS-102
  • 11. www.targovax.com Targovax has initiated a broad clinical program to test the clinical benefit of ONCOS-102 11 Initial Phase I trial Solid tumors 7 indications o 12 refractory patients o Monotherapy o Correlation between immune activation and survival Mesothelioma Phase I/II - controlled 30 patients Melanoma Phase I 12 patients Prostate Phase I 10 patients Ovarian / colorectal Phase I/II - controlled 78 patients o Combination with PD-1 CPI in refractory patients o Proof-of-concept o Memorial Sloan Kettering o Combination with chemo o Randomized controlled trial o Ultra-orphan indication o Collaboration with Ludwig & CRI o Combination with Medimmune’s durvalumab o Randomized controlled trial o Partnered with Sotio o Combination with DC therapy ONCOS TG Compassionate use program Finland 115 patients o Testing within ATAP EU program o Individual clinical responses o Reassuring safety data
  • 12. www.targovax.com Agenda 12 Introduction to immunotherapy ONCOS-102 oncolytic virus platform TG neo-antigen cancer vaccine platform Financial highlights Targovax clinical program overview
  • 13. www.targovax.com The survival rate for pancreatic cancer patients has not improved since the 1970s ONCOS TG No improvement in survival over the past 40 years Improvement in 10 year survival rate % change over 40yrs. 1972–2012 13
  • 14. www.targovax.com The RAS gene is mutated in >85% of pancreatic cancer patients, making it an interesting therapeutic target 14 One of the most common mutations in cancer RAS is a well-defined neoantigen Results in cell division permanently switched on No existing therapies targeting RAS Occurs in >85% of pancreatic cancer patients Incidence of RAS mutations ONCOS TG 100% 50% 0%
  • 15. www.targovax.com The TG neoantigen vaccine primes the immune system to recognize and destroy RAS mutated cancer cells 15 Activate immune system: o TG vaccine injected intradermally o APCs pick up the TG RAS antigens Train T-cells: o APCs present RAS antigens in lymph node o Production of RAS specific T-cells Attack the cancer: o RAS specific T-cells identify cancer cells displaying mutated RAS o CD8+ T-cells kill the cancer cells Cocktail of 7 peptides covering all relevant RAS mutations in pancreas ONCOS TG
  • 16. www.targovax.com The TG vaccine has shown 20% 10 year survival in earlier Phase I trials in resected pancreatic cancer 16 ONCOS TG 1 Wedén et al., 2011 2 Oettle H et al., JAMA 2007, vol 297, no 3 3 Oettle H et al., JAMA 2013, vol 310, no 14 0 10 20 30 40 50 60 70 80 90 100 0 6 12 18 24 30 36 42 48 54 60 66 72 78 84 90 96 102 108 114 120 o 4/20 (20%) treated patients alive after 10 years o 0/87 untreated patients alive in a similar cohort from the same period Survival(%) Months from resection 10 year survival from historical TG trials in resected pancreatic cancer (monotherapy)
  • 17. www.targovax.com These data were corroborated in a recent Phase I/II trial in combination with modern standard of care 17 Median survival 33.1 months from surgery 27.6 months for SoC (Gemcitabine) in ESPAC-4 study2 Immune response 18/19 patients (95%) showed TG specific immune activation Safety Good safety profile, treatment generally well-tolerated Some manageable allergic reactions were seen 2 year overall survival 13 of 19 patients (68%) alive 2 years after surgery Historical controls 2 year survival range from 30-53%1 1: Relevant historical control trials, not including ESPAC-4, which did not report 2 year OS 2: Based on ESPAC-4 reported 25.5 months median OS from randomisation, adding median time from surgery to randomization of 64 days (2.1 months) ONCOS TG Results from TG01-01 trial in resected pancreatic cancer (combination with Gemcitabine)
  • 18. www.targovax.com Clinical development overview for TG – Targovax is seeking potential partnership 18 Phase I/II Resected pancreatic cancer 32 patients o 10 year survival data o Correlation between immune response and survival o Large safety database Colorectal Phase I 20 patients Resected pancreas Phase II/III N=tbd o TG02, targets 8 mutations o Combination with Keytruda o Currently recruiting patients o 2 arm, controlled trial o Aimed to reach registration o Currently seeking partner ONCOS TG Phase I Resected & non-resected >200 patients Historical trials Planned / recruiting trialsCompleting trial o Encouraging 2 year survival and median survival
  • 19. www.targovax.com Agenda Introduction to immunotherapy ONCOS-102 oncolytic virus platform TG neo-antigen cancer vaccine platform Financial highlights Targovax clinical program overview 19
  • 20. www.targovax.com Two platforms and six clinical trials ensures a program with frequent data readouts 20 Cancer indication Combined with ONCOS-102 Melanoma CPI Mesothelioma Chemo* Orphan ind. Ovarian & Colorectal CPI Orphan ind. Sponsor: Ludwig Prostate DC therapy Sponsor: Sotio TG Resected Pancreatic Chemo* Orphan ind. Colorectal CPI 4 readouts 2017 5 readouts 2018 2017 2018 H1 H2 H1 H2 2019 H1 Phase l Phase l/ll Phase l Phase lb/ll Phase I/II Phase Ib Interim data Clinical, immune and safety data * In combination with Standard of Care Chemoterapy. Pemetrexed/cisplatin for Mesothelioma and Gemcitabine for Resected Pancreatic ONCOS TG Indicative timing of:
  • 21. www.targovax.com Agenda Introduction to immunotherapy ONCOS-102 oncolytic virus platform TG neo-antigen cancer vaccine platform Financial highlights Targovax clinical program overview 21
  • 22. www.targovax.com Targovax has a sound financial position, with cash to complete the planned clinical program into 2019 Operations Cash end of Q2 NOK 116m USD 14m June 30st 2017 Net cash flow NOK -32m USD -4m Total Q2 Annual run rate NOK 102m USD 12m Last four quarters Runway NOK ~300m USD >35m Into 2019 22 The share OSE: TRVX Market Cap NOK ~1bn USD ~125m At share price NOK ~20 Daily turnover NOK 5m USD 0.6m 6 month avg. Analysts DNB, ABG Sundal Collier, Arctic, Redeye, Norske Aksjeanalyser Raised NOK 200 million in private placement June 8 2017 10,000,000 new shares @ NOK 20 per share CORPORATE * Including preceeds from raise
  • 23. www.targovax.com The shareholder base is strong, with a mix of specialist, generalist and retail investors 23 CORPORATE Key international investors participating in PP 2017 – HealthCap (SWE) – Nyenburgh (NL) – Trium (UK) – Millenium Capital Partners (UK) – Interogo (SWE) – AP3 (SWE) – Aramea AM (DE) Shares and options ▪ 56.4m shares fully diluted – Average strike price on options ~NOK 21 – Total dilutive effect of options is 6.5% ▪ 52.5m ordinary shares – Management ownership: 1.7% – 3,880 shareholders Shareholder Shares m Relative HealthCap Sweden 12,4 23,6 % Nordea Norway 4,7 8,9 % RadForsk Norway 4,4 8,4 % KLP Norway 1,8 3,4 % Statoil Norway 1,2 2,2 % Rasmussengruppen Norway 1,0 1,9 % Danske Bank (nom.) Norway 0,8 1,6 % Euroclear Bank (nom.) Belgium 0,8 1,4 % Timmuno Norway 0,7 1,4 % Prieta AS Norway 0,7 1,4 % Thorendahl Invest AS Norway 0,7 1,3 % Sundt AS Norway 0,7 1,2 % The Bank of NY Mellon (nom.) Belgium 0,3 0,6 % ABN Amro Global (nom.) Netherland 0,3 0,5 % Norda ASA Norway 0,3 0,5 % NHO - P665AK Norway 0,3 0,5 % Yngve S. Lillesund Norway 0,2 0,4 % The Bank of NY Mellon (nom.) Belgium 0,2 0,4 % Tobech Invest AS Norway 0,2 0,4 % Istvan Molnar Norway 0,2 0,4 % Top 20 31,8 60,4 % Other shareholders (3860) 20,8 39,6 % Total 52,6 100,0 % Estimated ownership
  • 24. www.targovax.com Targovax has an experienced senior management team in place to execute the development program CEO - Øystein Soug o Previously CFO of Algeta ASA o Track record in bringing an oncology asset from phase I through to market launch o Oversaw the sale of Algeta to Bayer Healthcare CMO - Dr. Magnus Jäderberg o Former CMO of Bristol Myers Squibb Europe o Brought Yervoy to market as first- in-class checkpoint inhibitor o 25 years of experience in R&D CFO - Dr. Erik Digman Wiklund o Former consultant in McKinsey & Co Pharma practice o PhD in cancer research o Various roles in biotech, including at Algeta ASA CTO – Jon Amund Eriksen o Pinoeer in immuno-oncology o Original inventor of the RAS TG peptide platform o 35 years of experience in pharma R&D and product development CORPORATE
  • 25. www.targovax.com Planned strong news flow with multiple near term value inflection points 25 2015 2016 2017 2018H1 H2 phase ll initiated TG01 Immune activation and MoA demo ONCOS-102 Interim data pancreas TG01 (1st cohort) Immune activation pancreas TG01 (2nd cohort) 2-year survival pancreas TG01 (1st cohort) 2-year survival pancreas TG01 (2nd cohort) Initiate phase l/ll mesothelioma ONCOS-102 Initiate phase l prostate ONCOS-102 Initiate phase l/ll melanoma ONCOS-102 Interim data ovarian /colorectal ONCOS-102 phase l/ll data melanoma ONCOS-102 Interim data melanoma ONCOS-102 Interim data mesothelioma ONCOS-102 Initiate phase Ib in colorectal TG02 Interim data colorectal TG02 (mono) Initiate phase l Ovarian/colorectal ONCOS-102 Interim data prostate ONCOS-102 phase I data/ colorectal TG02 (combo) H1 H2 Listing on OSE main list Oslo Stock Exchange FINANCE