August 2017 Corporate Presentation

1. Investor Presentation
August 2017
www.oncolyticsbiotech.com TSX ONC OTCQX ONCYF

2. Forward Looking Statements
This presentation contains certain forward looking statements relating to the company’s
business prospects and the development and commercialization of REOLYSIN®, a first-in-class
systemically administered immuno-oncology agent for solid tumors and heme malignancies.
These statements are based on management’s current expectations and beliefs and are subject
to a number of factors which involve known and unknown risks, delays, uncertainties and other
factors not under the company’s control which may cause actual results, performance or
achievements of the company to be materially different from the results, performance or other
expectations implied by these forward looking statements.
In any forward looking statement in which Oncolytics Biotech® Inc. expresses an expectation or
belief as to future results, such expectations or beliefs are expressed in good faith and are
believed to have a reasonable basis, but there can be no assurance that the statement or
expectation or belief will be achieved. These factors include results of current or pending clinical
trials, risks associated with intellectual property protection, financial projections, actions by the
FDA/HPB/MHRA and those other factors detailed in the company’s filings with SEDAR and the
Securities and Exchange Commission. Oncolytics does not undertake an obligation to update
the forward looking statements, except as required by applicable laws.
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3. Rapid Recent Progress
 REOLYSIN® statistically significantly increased overall survival
(OS) in metastatic breast cancer (REO + paclitaxel vs. paclitaxel alone)
 Granted “Fast Track” designation by the FDA
 Strengthened management team:
 C-Suite and Business Development
 Announced collaboration with Myeloma UK and Celgene on
Phase 1b study of REOLYSIN in combination with Imnovid® or
Revlimid® as a rescue treatment for relapsing myeloma patients
 Defined Clinical Development Program & Registration Pathway
 Metastatic Breast Cancer
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4. What is REOLYSIN®?
 First-in-class systemically
administered immuno-
oncology viral agent for
solid tumors and
heme malignancies
 Non-pathogenic
proprietary isolate of the
unmodified reovirus
4

5. Pelareorep
administered to
patients via IV
In Normal Cells
In Cancer Cells
1. Direct Cell
Lysis
3. Adaptive Immune
Response2. Innate Immune
Response
Release
of TAA
& VAA
T-cell
activationActivation of
NK cells
APC
Release of
inflammatory
cytokines
2. Reolysin replication causes the
release of inflammatory cytokines
( ) which activate Natural Killer (NK)
cells, allowing NK cells to attack
cancer cells.
REOLYSIN® Mechanism of Action
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More than 40 supporting publications
1. Reolysin selectively replicates in
permissive cancer cells. Upon virus
replication, cancer cells lyse/die
releasing additional virus particles ( )
to infect nearby cancer cells.
In non-cancer cells Reolysin enters
the cells but is unable to replicate and
the virus is actively cleared.
3. Antigen presenting cells (APCs)
display tumor- and viral- associated
antigens ( ) to killer T-cells,
activating an adaptive anti-cancer
immune response.

6. What does REOLYSIN® do?
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1. Kills cancer cells stressed by
chemo and/or radiation
2. Induces PD-1 & PDL-1 expression
on T-cells and tumor-cells
3. Enhances IMiD targeting
4. Potentiator for all agents
affecting both innate and
adaptive immunity by making
cold tumors hot

7. REOLYSIN® MOA: Lessons Learned
• OS results support Mechanism of Action (MOA)
• OS trumps PFS (progression free survival)
• We’re not the only ones
o Opdivo®, Tecentriq® and Ipilimumab® have been approved on OS
1 Hodi, NEJM 2010, 363:711; 2 Borghaei, NEJM 2015,371:1627; 3 Ferris, NEJM 2016, 375:1856
Melanoma
treated with ICI
vs. chemo
Ipilimumab
SOC
Hodi et.al., NEJM 2010
Ipilimumab
SOC
Overall SurvivalProgression Free Survival
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8. Clinical Data &
Development Plan

9. Clinical Development Plan: Pathways
The clinical development plan addresses drug combinations that
can potentially boost each response of the MOA
1. Path 1 - Chemo combinations (direct cell lysis):
The basis for our metastatic breast cancer registration pathway.
2. Path 2 - Immunotherapy combinations (adaptive immune response):
Approaches with checkpoint inhibitors embodied in the ongoing
REOLYSIN® + pembrolizumab study and possible future collaborations.
3. Path 3 - Combination with IMiDs / targeted therapy (innate immune response):
Currently in combination with Celgene’s Imnovid® & Revlimid® in a first-of-its-
kind immunotherapy trial that aims to modulate the immune system to target
myeloma. Exploring additional collaborations.
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10. Path 1: Chemotherapy Combinations
Metastatic Pancreatic Cancer (1st Line)
Regulatory Status
o Orphan Drug Designation Granted (FDA / EMA)
o Potential for Fast-Track Designation
o Preparing for End-of-Phase 2 Meeting
Metastatic Breast Cancer
Regulatory Status
o Statistically significant phase 2 OS data
o Seeking scientific advice - potential for
Breakthrough Designation
o Preparing for End-of-Phase 2 Meeting
o Preparing registration pathway
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11. Path 1: Chemo-Combo / Breast Cancer
• Randomized, non-blinded study, with IV
administered REOLYSIN® given in
combination with paclitaxel versus
paclitaxel alone
• Patients with advanced or metastatic breast
cancer
• Paclitaxel weekly, on days 1, 8 and 15 of a
28-day cycle and test arm with the addition
of REOLYSIN® on days 1, 2, 8, 9, 15 and 16
• 74 patients; powered to 90%
• Endpoints:
• Primary: PFS
• Secondary: OS
• Secondary : ORR
• Secondary: Safety
(IND-213) Phase 2 Data(IND-213) Phase 2 Design
• ORR and PFS similar in both groups
• Statistically significant improvement
in median OS:
• 10.4 months to 17.4 months
• 60 patients presented APC Wild Type
• OS doubled from 10.4 months to
~ 20.9 months
• First immuno-oncology viral-agent to
demonstrate a statistically significant
median OS advantage in a
randomized clinical study
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12. Path 1: Chemo-Combo / Breast Cancer
Statistically significantly increased overall
survival in metastatic breast cancer in ITT group
Canadian Cancer Trials Group
Test n=36
Control n=38
HR = 0.65
p = 0.1 (powered to 90%)
Test = REO + paclitaxel
Control = paclitaxel
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13. Path 1: Chemo-Combo / Breast Cancer
Canadian Cancer Trials Group
Test n=31
Control n=29
HR = 0.53
p = 0.03
Test = REO + paclitaxel
Control = paclitaxel
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Doubled overall survival APC wild type patients

14. Path 1: Chemo-Combo / Breast Cancer
Key Learnings
 Consistent with other approved I/O therapies, REOLYSIN® acts as an immune
therapy agent, often with no meaningful improvement in either PFS or ORR
 Has the potential to work synergistically with paclitaxel
Next Steps
 Seeking scientific advice - potential for Breakthrough Designation
 Preparing for End-of-Phase 2 Meeting
 Preparing registration pathway in metastatic breast cancer
14

15. 15
115,405
addressable patient
population on
target therapies
(74% of mBC patients)
Source: https://seer.cancer.gov/statfacts/html/breast.html.Accessed on March 28, 2017.
Howlader, Nadia,et al. US Incidenceof Breast Cancer Subtypes Defined by Joint Hormone
Receptor and HER2 Status. Journal of the NationalCancer Institute.Accessed March 28, 2017
3,560,570
breast cancer prevalence, US 2016
2,599,216
Patients with HR+/HER2- Subtype
155,953
Patients diagnosed with stage IV
breast cancer
Path 1: Chemo-Combo / Breast Cancer

16. Path 1: Supporting OS as Registration Endpoint
Doubling 2-year survival in phase 2 studies
Randomized Intention-to-Treat (NCI-8601)
o Carbotax + REO (n=36)
o Carbotax (n=37)
Randomized Excluding Crossover
o Carbotax + REO (n=36)
o Carbotax (n=20)
Single Arm (REO 017)
o REO + Gemcitabine
(n=34)
Reo + gem
2y-OS = 24 %
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17. Path 2: Immunotherapy Combinations
REO + Pembrolizumab (anti-PD-1 antibody)
in pancreatic cancer (REO 024)
o Establish safety profile
o Final analysis in 2017
Future potential collaborations pending
Rajani, Viruses 2015, 7:588; Noonan, Mol Ther 2016;
Rajani, Mol Ther 2016,24:166
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18. Path 3: Targeted/IMiD Combinations
REO + Pomalidomide in multiple myeloma
o Establish safety profile
o Ongoing collaboration with Celgene
& Myeloma UK
o Combined with Revlimid® & Imnovid® as a
rescue treatment in myeloma patients
Enhancement of Innate Immune
Response:
REOLYSIN® + IMiDs
REOLYSIN® alone
REOLYSIN® + IMiDs
Release of
inflammatory
cytokines
Increased
activation of
NK cells
Release of
inflammatory
cytokines
Activation of
NK cells
+ IMiDs
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19. Safety, Manufacturing
& Intellectual Property

20. REOLYSIN® and Safety
 1,100+ patients treated, 900+ intravenously
 No maximum tolerated dose (MTD) reached to date
Monotherapy Toxicity Symptoms
Symptoms frequently observed from day 2 of treatment
and usually lasted < 6 hours
Intravenous local
 Toxicities have generally been mild (grade 1 or 2) and included chills, fever,
headache, cough, myalgia, runny nose, sore throat, fatigue, and grade 1 or 2
lymphopenia or neutropenia
 Transient grade 3 and 4 toxicities included lymphopenia or neutropenia
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21. Manufacturing
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 Final formulation produced at 100
Liter-scale under cGMP
 > 50,000 standard doses per
production run
 Commercial scale manufacturing
agreement with SAFC (part of Merck
Millipore Sigma)
 When stored frozen, liquid
formulation is stable for at least five
years (stability testing ongoing)

22. Patent Portfolio
 More than 415 patents issued
worldwide, including 61 US and
20 Canadian
 Reovirus issue patent claims cover:
• Compositions of matter comprising reovirus
• Through 2028
• Pharmaceutical use of reoviruses to treat
neoplasia and cellular proliferative diseases
• Combination therapy with radiation,
chemotherapy and/or immune suppressants
• Methods for manufacturing reovirus and
screening for susceptibility to reovirus
• Pharmaceutical use of reoviruses in
transplantation procedures
 Over 60 pending
applications worldwide
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23. Corporate & Financial

24. Experienced Leadership
Matt Coffey, PhD, MBA
Co-founder, Director,
President & CEO
Kirk Look, CA
Chief Financial Officer
EY LLP
Andres Gutierrez, MD, PhD
Chief Medical Officer
Bristol-Myers Squibb
Andrew de Guttadauro
VP of Business Development
Amgen, Biogen, Takeda
Wayne Pisano, MBA
Chairman of the Board, Oncolytics
Former President, Sanofi Pasteur
Angela Holtham, MBA, ICD.D
Nabisco
Hospital for Sick Children
J. Mark Lievonen, CA
Former President, Sanofi Pasteur
Ontario Institute for Cancer Research
William G. Rice, PhD
President & CEO, Aptose Biosciences
President, CEO & Director of Achillion
Bernd R. Seizinger, MD, PhD
Former President & CEO of GPC Biotech
VP of Oncology Drug Discovery, BMS
Non-Executive Directors
Extensive knowledge of oncology/immunotherapy | Public company experience
Strong business development and commercialization expertise
Management
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25. Milestones
Event Timing
New Leadership Team
Collaboration with Myeloma UK & Celgene
More than doubled 2 year survival in pancreatic cancer
Statistically significantly increased OS in metastatic breast cancer
Fast Track Designation
End-of-Phase 2 Meeting for mBC Mid ’17
Regulatory milestones (including break through status for mBC) 2H
Additional pharma research collaborations (IO’s and IMiD’s) 2H
Projected Registration Partnership 1H 2018
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26. Market and Capital Data
Exchanges
OTCQX: ONCYF
TSX: ONC
Market Cap (August 4, 2017)
USD $50.5 M
CDN $69.6 M
Shares Outstanding (August 2, 2017) 139,426,222
Warrants (August 2, 2017)
Options (August 2, 2017)
Restricted/performance share units (August 2, 2017)
16,445,000
7,532,827
2,370,388
Fully Diluted (August 2, 2017) 165,774,437
Cash / Cash Equivalents /
Short Term Investments (June 30, 2017)
CDN $16.7 million
USD $13.2 million*
Cash runway End of 2018
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* Based on FX on June 1, 2017

27. Investment Highlights
 REOLYSIN® statistically significantly increased overall survival (OS) in
metastatic breast cancer (REO + paclitaxel vs. paclitaxel alone)
 Granted “Fast Track” designation by the FDA
 Strengthened management team: C-Suite and Business Development
 Unpartnered immuno-oncology viral agent for systemic
administration exploiting dual activity by cancer cell lysis and anti-
tumor immunity
 Defined Clinical Development Program & Registration Pathway
 Extensive patient safety data showing no added significant toxicity
when used as combination with chemotherapy
 Manufacturing at commercial scale with sufficient supplies on hand to
support late- stage development and early commercialization
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28. Investor Presentation
www.oncolyticsbiotech.com TSX ONC OTCQX ONCYF