SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 
Form 6-K
 
Report of Foreign Private Issuer
 
Pursuant to Rule 13a-16 or 15d-16
of the Securities Exchange Act of 1934
 
For the month of November 2019

Commission File Number 001-38512
 
Oncolytics Biotech Inc.
 
(Translation of registrant’s name into English)
 
Suite 210, 1167 Kensington Crescent NW
Calgary, Alberta, Canada T2N 1X7
 
(Address of principal executive offices)
 
Indicate by check mark whether the registrant files or will file annual reports under cover Form 20-F or Form 40-F.
Form 20-F   þ
 
Form 40-F   o
 
Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1):   o
 
Note: Regulation S-T Rule 101(b)(1) only permits the submission in paper of a Form 6-K if submitted solely to provide an attached annual report to security holders.
 
Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7):   o
 
Note: Regulation S-T Rule 101(b)(7) only permits the submission in paper of a Form 6-K if submitted to furnish a report or other document that the registrant foreign private issuer must furnish and make public under the laws of the jurisdiction in which the registrant is incorporated, domiciled or legally organized (the registrant’s “home country”), or under the rules of the home country exchange on which the registrant’s securities are traded, as long as the report or other document is not a press release, is not required to be and has not been distributed to the registrant’s security holders, and, if discussing a material event, has already been the subject of a Form 6-K submission or other Commission filing on EDGAR.
 
INCORPORATION BY REFERENCE
 
The Registrant’s Management’s Discussion and Analysis of Operations and Financial Condition for the Three and Nine Months Ended September 30, 2019, included as Exhibit 99.2 of this Form 6-K and the Interim Financial Statements as of and for the Three and Nine Months Ended September 30, 2019, included as Exhibit 99.1 of this Form 6-K (Commission File No. 001-38512), furnished to the Commission on November 12, 2019, are incorporated by reference into the Registrant’s Registration Statement on Form F-10 (Commission File No. 333-224432).









EXHIBIT
NUMBER
 
DESCRIPTION
 
 
 
99.1
 
99.2
 
99.3
 
99.4
 


SIGNATURES
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
 
 
 
Oncolytics Biotech Inc.
(Registrant)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Date: November 12, 2019
 
By:
 
/s/  Kirk Look

Kirk Look
Chief Financial Officer

























Interim Consolidated Financial Statements
(unaudited)

Oncolytics Biotech® Inc.
September 30, 2019 and 2018





ONCOLYTICS BIOTECH INC.
INTERIM CONSOLIDATED STATEMENTS OF FINANCIAL POSITION
(unaudited)

As at
Notes
September 30,
2019
$
December 31,
2018
$
Assets
 
 

 

Current assets
 
 

 

Cash and cash equivalents
4
12,298,678

13,699,881

Other receivables
10
458,186

51,650

Prepaid expenses
 
2,681,274

700,986

Total current assets
 
15,438,138

14,452,517

Non-current assets
 
 

 

Property and equipment

321,611

412,736

Right-of-use assets
3
525,508


Total non-current assets
 
847,119

412,736







Total assets
 
16,285,257

14,865,253

Liabilities And Shareholders’ Equity
 
 

 

Current Liabilities
 
 

 

Accounts payable and accrued liabilities
 
3,725,469

1,825,853

Contract liability
9

927,400

Other liabilities
3

61,322

Lease liabilities
3
358,435


Total current liabilities
 
4,083,904

2,814,575

Non-current liabilities
 
 
 
Contract liability
9
6,730,287

5,802,887

Other liabilities
3

52,428

Lease liabilities
3
245,703


Warrant derivative
5, 12
1,774,210


Total non-current liabilities

8,750,200

5,855,315

 
 
 
 
Total liabilities

12,834,104

8,669,890

Commitments and contingencies
10




Shareholders’ equity
 
 

 

Share capital
  Authorized: unlimited
  Issued: September 30, 2019 – 25,039,920
December 31, 2018 – 17,399,749
6
295,555,692

285,193,061

Warrants
6
3,617,570

3,617,570

Contributed surplus
7
28,961,667

28,260,613

Accumulated other comprehensive income

520,855

607,504

Accumulated deficit

(325,204,631
)
(311,483,385
)
Total shareholders’ equity
 
3,451,153

6,195,363

Total liabilities and equity
 
16,285,257

14,865,253

See accompanying notes

2






ONCOLYTICS BIOTECH INC.
INTERIM CONSOLIDATED STATEMENTS OF LOSS AND COMPREHENSIVE LOSS
(unaudited)

 
Notes
Three Month Period Ending September 30, 2019
$
Three Month Period Ending September 30, 2018
$
Nine Month Period Ending September 30, 2019
$
Nine Month Period Ending September 30, 2018
$
 
 
 
 
 
 
Expenses
 
 
 
 

 

   Research and development
7, 14, 15
1,618,126

1,929,405

8,323,994

6,909,713

   Operating
7, 14, 15
1,834,021

1,468,262

5,426,093

4,869,617

Loss before the following
 
(3,452,147
)
(3,397,667
)
(13,750,087
)
(11,779,330
)
   Change in fair value of warrant derivative
5
(122,498
)

(122,498
)

   Interest income, net
 
46,001

61,880

151,339

109,308

Loss before income taxes
 
(3,528,644
)
(3,335,787
)
(13,721,246
)
(11,670,022
)
   Income tax expense


(79
)

(547,957
)
Net loss
 
(3,528,644
)
(3,335,866
)
(13,721,246
)
(12,217,979
)
Other comprehensive income (loss) items that may be reclassified to net loss

 
 




  Translation adjustment

38,306

(49,238
)
(86,649
)
85,412

Net comprehensive loss

(3,490,338
)
(3,385,104
)
(13,807,895
)
(12,132,567
)
Basic and diluted loss per common share
8
(0.16
)
(0.20
)
(0.67
)
(0.78
)
Weighted average number of shares (basic and diluted)
8
22,642,016

16,540,612

20,431,792

15,646,117

See accompanying notes

3




ONCOLYTICS BIOTECH INC.
INTERIM CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY
(unaudited)


Notes
Share Capital
$
Warrants
$
Contributed Surplus
$
Accumulated Other Comprehensive Income
$
Accumulated Deficit
$
Total
$
As at December 31, 2017
 
271,710,138

3,617,900

27,028,238

373,730

(294,446,160
)
8,283,846

Net loss and other comprehensive income
 



85,412

(12,217,979
)
(12,132,567
)
Issued pursuant to "At the Market" Agreement
6
553,650





553,650

Issued pursuant to public offering
6
11,606,882





11,606,882

Issued pursuant to Common Stock Purchase Agreement
6
1,906,152





1,906,152

Issued pursuant to stock option plan
7
178,322


(66,635
)


111,687

Issued pursuant to warrant agreement
6
1,747

(330
)



1,417

Share based compensation
7


932,817



932,817

Share issue costs
6
(2,214,482
)




(2,214,482
)
As at September 30, 2018
 
283,742,409

3,617,570

27,894,420

459,142

(306,664,139
)
9,049,402

 
 
 
 
 
 
 
 
As at December 31, 2018
 
285,193,061

3,617,570

28,260,613

607,504

(311,483,385
)
6,195,363

Net loss and other comprehensive income
 



(86,649
)
(13,721,246
)
(13,807,895
)
Issued pursuant to incentive share award plan
7
110,437


(110,437
)



Issued pursuant to Common Stock Purchase Agreement
6
3,562,608





3,562,608

Issued pursuant to "At the Market" Agreement
6
4,034,933





4,034,933

Issued pursuant to public offering
5, 6
3,314,429





3,314,429

Share based compensation
7


811,491



811,491

Share issue costs
6
(659,776
)




(659,776
)
As at September 30, 2019
 
295,555,692

3,617,570

28,961,667

520,855

(325,204,631
)
3,451,153

See accompanying notes


4






ONCOLYTICS BIOTECH INC.
INTERIM CONSOLIDATED STATEMENTS OF CASH FLOWS
(unaudited)
 
 
 
Notes
Three Month Period Ending September 30, 2019
$
Three Month Period Ending September 30, 2018
$
Nine Month Period Ending September 30, 2019
$
Nine Month Period Ending September 30, 2018
$

 
 
 
 

 

Operating Activities
 
 
 
 

 

Net loss for the period
 
(3,528,644
)
(3,335,866
)
(13,721,246
)
(12,217,979
)
Depreciation - property and equipment
14
24,483

26,698

98,190

67,682

Depreciation - right-of-use-assets
3, 14
90,522


272,201


Share based compensation
7, 14, 15
250,384

236,607

811,491

932,817

Interest expense on lease liabilities
3
24,822


73,399


Unrealized foreign exchange (gain) loss

(9,865
)
82,643

104,425

(19,702
)
Onerous lease contract
14

67,588


67,588

Amortization - lease incentive liability
14

12,494


12,494

Change in fair value of warrant derivative
5
122,498


122,498


Net change in non-cash working capital
13
(1,491,146
)
(596,779
)
(412,173
)
3,630,991

Cash used in operating activities
 
(4,516,946
)
(3,506,615
)
(12,651,215
)
(7,526,109
)
Investing Activities
 
 
 
 

 

Acquisition of property and equipment
 

(40,094
)
(9,660
)
(120,156
)
Cash used in investing activities
 

(40,094
)
(9,660
)
(120,156
)
Financing Activities
 
 
 
 

 

Proceeds from exercise of stock options
7

87,777


111,687

Proceeds from exercise of warrants
6



1,417

Proceeds from Common Stock Purchase Agreement
6

1,143,361

3,529,672

1,143,361

Proceeds from "At the Market" equity distribution agreement
6
55,015


3,874,377

520,315

Proceeds from public offering
6
4,505,359


4,505,359

10,188,526

Payment of lease liabilities
3
(112,070
)

(334,872
)

Cash provided by financing activities
 
4,448,304

1,231,138

11,574,536

11,965,306

(Decrease) increase in cash
 
(68,642
)
(2,315,571
)
(1,086,339
)
4,319,041

Cash and cash equivalents, beginning of period
 
12,275,766

18,741,347

13,699,881

11,836,119

Impact of foreign exchange on cash and cash equivalents
 
91,554

(211,429
)
(314,864
)
59,187

Cash and cash equivalents, end of period
 
12,298,678

16,214,347

12,298,678

16,214,347

See accompanying notes

5


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019


Note 1: Incorporation and Nature of Operations
 
Oncolytics Biotech Inc. was incorporated on April 2, 1998 under the Business Corporations Act (Alberta) as 779738 Alberta Ltd. On April 8, 1998, we changed our name to Oncolytics Biotech Inc.

Our interim consolidated financial statements for the period ended September 30, 2019, were authorized for issue in accordance with a resolution of the Board of Directors (the "Board") on November 12, 2019. We are a limited company incorporated and domiciled in Canada. Our shares are publicly traded on the Nasdaq Capital Markets and the Toronto Stock Exchange. Our registered office is located at 210, 1167 Kensington Crescent NW, Calgary, Alberta, Canada.

We are a development stage biopharmaceutical company that focuses on the discovery and development of pharmaceutical products for the treatment of cancers that have not been successfully treated with conventional therapeutics. Our lead product, pelareorep, is a potential immuno-oncology viral-agent that may be a novel treatment for certain types of cancer and may be an alternative to existing cytotoxic or cytostatic therapies. Our clinical development program for pelareorep emphasizes three programs: chemotherapy combinations to assist the escape of the virus from the vasculature and enhance its distribution in the tumor; immuno-therapy combinations to create an inflamed phenotype promoting synergies with immune checkpoint inhibitors; and immune modulator/targeted combinations to upregulate natural killer cells promoting synergies with targeted therapies.

Note 2: Basis of Financial Statement Presentation

Our interim consolidated financial statements include our financial statements and the financial statements of our subsidiaries as at September 30, 2019 and are presented in Canadian dollars, our functional currency.
Our accounts are prepared in accordance with International Financial Reporting Standards ("IFRS") issued by the International Accounting Standards Board ("IASB"). The accounts are prepared on the historical cost basis, except for certain assets and liabilities which are measured at fair value as explained in the notes to these financial statements.
These interim consolidated financial statements have been prepared in compliance with International Accounting Standard 34 Interim Financial Reporting. The notes presented in these interim consolidated financial statements include only significant events and transactions occurring since our last fiscal year end and are not fully inclusive of all matters required to be disclosed in our annual audited consolidated financial statements. Accordingly, these interim consolidated financial statements should be read in conjunction with our most recent annual audited consolidated financial statements, for the year ended December 31, 2018. We have consistently applied the same accounting policies for all periods presented in these interim consolidated financial statements as those used in our audited consolidated financial statements for the year ended December 31, 2018, except for the adoption of new standards effective as of January 1, 2019.

Note 3: Significant Accounting Policies

Adoption of New Accounting Standards

IFRS 16 Leases

IFRS 16 Leases (“IFRS 16”) replaces IAS 17 Leases (“IAS 17”) and related interpretations for annual periods beginning on or after January 1, 2019. We have adopted IFRS 16 using the modified retrospective approach, under which the cumulative effect of the initial application is recognized in retained earnings at January 1, 2019. We have not restated comparatives for 2018. On transition to IFRS 16, we elected to apply the following practical expedients:

Applied the exemption for short-term leases that have a remaining lease term of less than 12 months as at January 1, 2019;
Excluded initial direct costs for the measurement of right-of-use assets as at January 1, 2019;

6


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Relied upon our assessment of whether leases are onerous under the requirement of IAS 37, Provisions, contingent liabilities and contingent assets as at December 31, 2018 as an alternative to reviewing our right-of-use assets for impairment; and
Measured the right-of-use assets at an amount equal to the lease liability, adjusted by the amount of lease incentive liability related to that lease recognized in the statement of financial position immediately before the date of initial application.

We have elected not to separate fixed non-lease components from lease components and instead account for each lease component and associated fixed non-lease components as a single lease component.

On transition to IFRS 16, the Company recognized $882,437 of lease liabilities. Lease liabilities have been measured by discounting future lease payments using the Company's incremental borrowing rate at January 1, 2019 as rates implicit in the leases were not readily determinable. The weighted-average rate applied was 15%.

The following table summarizes the impacts of adopting IFRS 16 on the consolidated financial statements:
 
Impact of changes
 
As reported as at December 31, 2018
Effects of IFRS 16 transition
Subsequent to transition as at January 1, 2019
Right-of-use assets

808,025

808,025

Other current and non-current assets
14,865,253


14,865,253

Total assets
14,865,253

808,025

15,673,278

Other liabilities
113,750

(74,412
)
39,338

Lease liabilities

882,437

882,437

Other current and non-current liabilities
8,556,140


8,556,140

Total liabilities
8,669,890

808,025

9,477,915

Total shareholders' equity
6,195,363


6,195,363


Prior to adopting IFRS 16, our total minimum operating lease commitments as at December 31, 2018 were $961,575. The difference between the total of the minimum lease payments set out in Note 11 of our 2018 annual consolidated financial statements and the total lease liabilities recognized on transition was a result of the effect of discounting on the minimum lease payments.

Explanatory information
Our portfolio of leases consists of office spaces. We currently do not have leases with variable lease payments, residual value guarantees, extension or termination options, or leases not yet commenced to which we are committed. Our total undiscounted lease liability as at September 30, 2019 is as follows:
Maturity analysis - contractual undiscounted cash flows
September 30, 2019
 
Less than one year
423,521

One to five years
261,801

More than five years

Total undiscounted lease liability as at September 30, 2019
685,322










7


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Accounting policy
At inception of a contract, we assess whether a contract is, or contains a lease by determining whether the contract conveys the right to control the use of an identified asset for a period of time in exchange for consideration. To assess whether a contract conveys the right to control the use of an identified asset, we assess whether:

the contract involves the use of an identified asset;
we have the right to obtain substantially all of the economic benefits from use of the identified asset throughout the period of use; and
we have the right to direct the use of the identified asset.

A right-of-use asset and corresponding lease liability is recognized on the lease commencement date. The right-of-use asset is initially measured at cost, which comprises the initial amount of the lease liability adjusted for any lease payments made at or before the commencement date, plus any initial direct costs incurred and an estimate of costs to dismantle and remove the underlying asset or to restore the underlying asset or the site on which it is located, less any lease incentives received. The right-of-use asset is subsequently depreciated using the straight-line method from the commencement date to the end of the lease term. In addition, the right-of-use asset is reduced by impairment losses and adjusted for certain remeasurements of the lease liabilities, if any.

The lease liability is initially measured at the present value of the lease payments that are not paid at the commencement date. The lease payments are discounted using the implicit interest rate in the lease. If the rate cannot be readily determined, our incremental rate of borrowing is used. The lease liability is subsequently measured at amortized cost using the effective interest method. The lease liability is remeasured when there is a change in future lease payments arising from a change in an index or rate, if there is a change in our estimate of the amount expected to be payable under a residual value guarantee, if we change our assessment of whether we will exercise a purchase, extension or termination option, or if the underlying lease contract is amended.

We have elected not to separate fixed non-lease components from lease components and instead account for each lease component and associated fixed non-lease components as a single lease component.

We have elected not to recognize right-of-use assets and lease liabilities for short-term leases that have a lease term of 12 months or less. We recognize the lease payments associated with these leases as an expense on a straight-line basis over the lease term.

Significant Judgments, Estimates and Assumptions
We make judgments in determining whether a contract contains an identified asset. The identified asset should be physically distinct or represent substantially all of the capacity of the asset, and should provide us with the right to substantially all of the economic benefits from the use of the asset.

We also make judgments in determining whether or not we have the right to control the use of the identified asset. We have that right when we have the decision-making rights that are most relevant to changing how and for what purpose the asset is used. In rare cases where the decisions about how and for what purpose the asset is used are predetermined, we have the right to direct the use of the asset if we have the right to operate the asset or if we designed the asset in a way that predetermines how and for what purpose the asset will be used.

We make judgments in determining the incremental borrowing rate used to measure our lease liability for each lease contract, including an estimate of the asset-specific security impact. The incremental borrowing rate should reflect the interest that we would have to pay to borrow at a similar term and with a similar security.

Note 4: Cash Equivalents
 
Cash Equivalents
Cash equivalents consist of interest bearing deposits with our bank totaling $9,610,737 (December 31, 2018$9,977,409).  The current annual interest rate earned on these deposits is 2.69% (December 31, 20182.71%).




8


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Note 5: Warrant Derivative

On August 16, 2019, pursuant to an underwritten public offering, 4,619,773 units were sold at a purchase price of US$0.81 per unit for gross proceeds of US$3,742,016. Each unit included one common share and one common share purchase warrant (see Note 6). Each common share purchase warrant entitles the holder to purchase one common share at an exercise price of US$0.90 until August 16, 2024. We incurred transaction costs of $699,427 of which $466,284 were allocated to share issue costs and $233,143 were allocated to operating expenses, based on their relative fair values.

Under IFRS 9 Financial Instruments and IAS 32 Financial Instruments: Presentation, warrants with an exercise price denominated in a currency that differs from an entity's functional currency are treated as a derivative measured at fair value with subsequent changes in fair value accounted for through the consolidated statement of loss. Our warrants with an exercise price of US$0.90 meet this requirement and we have presented the value of these warrants as a non-current liability on the consolidated statement of financial position. Upon exercise, the recorded liability will be included in our share capital along with the proceeds from the exercise. If these warrants expire, the related liability is reversed through the consolidated statement of loss. There is no cash flow impact as a result of the accounting treatment for changes in the fair value of the warrant derivative or when warrants expire unexercised.

Estimating the fair value for our warrant derivative requires determining the most appropriate valuation model which is dependent on the terms and conditions of the issuance. This estimate also requires determining the most appropriate inputs to the valuation model, including the expected life of the warrant derivative, expected share price volatility and expected dividend yield and making assumptions about them.

A reconciliation of the change in fair value of the warrant derivative is as follows:
 
Fair Value of Warrant Derivative
Balance, August 16, 2019
1,657,214

Change in fair value of warrant derivative
122,498

Foreign exchange impact
(5,502
)
Balance, September 30, 2019
1,774,210

The estimated fair value of the warrant derivative issued during the period was determined using the Black-Scholes valuation model using the following assumptions:
 
September 30, 2019
August 16, 2019
Fair value of warrants
US$0.29
US$0.27
Risk-free interest rate
1.55%
1.42%
Expected hold period to exercise
4.0 years
4.0 years
Expected share price volatility
83.00%
82.00%
Expected dividend yield
Nil
Nil

We use historical data to estimate the expected dividend yield and expected volatility of our stock in determining the fair value of the warrants. The risk-free interest rate is based on U.S. Department of Treasury benchmark treasury yield rates in effect at the time of valuation and the expected life of the warrants represents the estimated length of time the warrants are expected to remain outstanding.

The following table summarizes our outstanding warrant derivative at September 30, 2019:
Exercise Price
Outstanding, Beginning of the Period
Granted During the Period
Outstanding, End of the Period
Weighted Average Remaining Contractual Life (years)
US$0.90

4,619,773

4,619,773

4.88



9


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Note 6: Share Capital
Authorized:
Unlimited number of no par value common shares

Share Consolidation:
On May 22, 2018, we completed the consolidation of our common shares on the basis of 9.5 pre-consolidation common shares for each one post-consolidation common share (the "Share Consolidation"). Fractional interests were rounded down to the nearest whole number of common shares. Outstanding stock options, restricted share units and performance share units were similarly adjusted by the consolidation ratio. Outstanding warrants were adjusted such that, following the Share Consolidation, 9.5 warrants issued in 2017 will entitle the holder to purchase one whole common share until June 1, 2022.
Issued:
Shares
Warrants
 
Number
Amount
$
Number
Amount
$
Balance, December 31, 2017
141,805,722

271,710,138

16,445,000

3,617,900

Issued pursuant to "At the Market" equity distribution agreement(a)
519,500

553,650



Share issue costs

(33,335
)


Issued pursuant to stock option plan
71,000

38,269



Balance, May 22, 2018 - pre-consolidation
142,396,222

272,268,722

16,445,000

3,617,900

Balance, May 22, 2018 - post-consolidation
14,988,995

272,268,722

16,445,000

3,617,900

Issued pursuant to public offering(b)
1,532,278

11,606,882



Issued pursuant to warrant agreement
157

1,747

(1,500
)
(330
)
Issued pursuant to stock option plan
34,329

158,976



Issued pursuant to incentive share award plan
28,297

109,751



Issued pursuant to Common Stock Purchase Agreement(c)
797,691

3,314,097



Issued pursuant to "At the Market" equity distribution agreement(d)
18,002

66,360



Share issue costs

(2,333,474
)


Balance, December 31, 2018
17,399,749

285,193,061

16,443,500

3,617,570

Issued pursuant to incentive share award plan
57,281

110,437



Issued pursuant to Common Stock Purchase Agreement(c)
1,390,372

3,562,608



Issued pursuant to "At the Market" equity distribution agreement(d)
1,572,745

4,034,933



Issued pursuant to public offering(e)
4,619,773

3,314,429



Share issue costs

(659,776
)


Balance, September 30, 2019
25,039,920

295,555,692

16,443,500

3,617,570


(a)
On February 25, 2016, we entered into an ATM equity distribution agreement with Canaccord Genuity Inc. acting as our sole agent with an aggregate offering value of up to $4.6 million which allowed us to sell our common shares through the facilities of the Toronto Stock Exchange or other "marketplace” (as defined in National Instrument 21-101 Marketplace Operation) in Canada (our "Canadian ATM"). During the period ending September 30, 2018, we sold 519,500 pre-consolidation shares (approximately 54,682 post-consolidation shares) for gross proceeds of $553,650. We incurred share issue costs of $33,335.

(b)
On June 5, 2018, pursuant to an underwritten public offering, 1,532,278 common shares were sold at a purchase price of US$5.83 per share for gross proceeds of US$8,933,181. We incurred share issue costs of $1,418,356.

10


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

(c)
On September 27, 2018, we entered into a Common Stock Purchase Agreement (the "Agreement") with Lincoln Park Capital Fund, LLC ("LPC"). Subject to the terms and conditions of the Agreement and at our sole discretion, we may sell up to US$26,000,000 worth of common shares to LPC over the 30-month term. The purchase price of the common shares will be based on the prevailing market prices immediately preceding the notice of sale without any fixed discount. Subject to the terms of the Agreement, we control the timing and amount of any future investment and LPC is obligated to make such purchases, if and when we elect. The Agreement does not impose any upper price limit restrictions, negative covenants or restrictions on our future financing activities. However, in no event will shares be sold to LPC on a day the closing sale price for the common shares is less than the floor price of US$1.00 per common share; or at a price per share that is less than the volume weighted average trading pricing of the common shares on the TSX for the five immediately preceding trading days, less the maximum applicable discount allowed by the TSX. We can terminate the Agreement at any time at our sole discretion without any monetary cost or penalty.

During the period ending September 30, 2019, we sold 1,379,024 (September 30, 2018 - 248,762) common shares for gross proceeds of US$2,663,768 (September 30, 2018 - US$1,000,000) and issued 11,348 commitment shares (September 30, 2018 - 115,014). The commitment shares have been valued at fair value of US$21,998 (September 30, 2018 - US$472,501) and have been recorded as share issue costs in addition to cash share issue costs of $3,757 (September 30, 2018 - $151,139).

(d)
On October 24, 2018, we entered into an ATM equity offering sales agreement with Canaccord Genuity Inc. The ATM allows us, at our sole discretion, to issue common shares, at prevailing market price, with an aggregate offering value of up to US$30,000,000 over a 19-month period through the facilities of the Nasdaq Capital Market in the United States. During the period ending September 30, 2019, we sold 1,572,745 common shares (September 30, 2018 - nil) for gross proceeds of US$3,030,892 (September 30, 2018 - nil). We incurred share issue costs of $160,556 (2018 - nil).

(e)
On August 16, 2019, pursuant to an underwritten public offering, 4,619,773 units were sold at a purchase price of US$0.81 per unit for gross proceeds of US$3,742,016. Each unit included one common share with a fair value of US$0.54 and one common share purchase warrant with a fair value of US$0.27 (see Note 5). Each common share purchase warrant entitles the holder to purchase one common share at an exercise price of US$0.90 until August 16, 2024. We incurred transaction costs of $699,427 of which $466,284 were allocated to share issue costs and $233,143 were allocated to operating expenses, based on their relative fair values.

Warrants

The following table summarizes our outstanding equity warrants at September 30, 2019:
Exercise Price
Outstanding, Beginning of the Period
Outstanding, End of the Period(1)
Weighted Average Remaining Contractual Life (years)
$
9.025

16,443,500

16,443,500

2.67

(1) Exercisable into 1,730,894 common shares.











11


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Note 7: Share Based Payments
Stock Option Plan
We have issued stock options to acquire common stock through our stock option plan of which the following are outstanding at September 30:
 
2019
2018
 
Stock Options
Weighted Average Exercise Price
$
Stock Options
Weighted Average Exercise Price
$
Outstanding, beginning of the period
1,249,361

8.73
647,156

13.20
Granted during the period
20,000

2.12
327,467

7.38
Forfeited during the period
(9,787
)
13.64
(90,817
)
11.74
Exercised during the period

(37,592
)
2.97
Outstanding, end of the period
1,259,574

8.58
846,214

11.56
Options exercisable, end of the period
854,129

10.56
598,222

13.56

The following table summarizes information about the stock options outstanding and exercisable at September 30, 2019:
Range of Exercise Prices
Number Outstanding
Weighted Average Remaining Contractual Life (years)
Weighted Average Exercise Price
$
Number Exercisable
Weighted Average Exercise Price
$
$2.12 - $3.99
731,827

5.2
3.18
452,494

3.24
$4.84 - $7.81
329,777

3.0
7.21
203,665

7.13
$13.77 - $19.00
90,203

4.0
16.95
90,203

16.95
$20.23 - $36.96
49,410

2.1
32.56
49,410

32.56
$38.09 - $63.84
58,357

2.2
50.85
58,357

50.85
 
1,259,574

4.3
8.58
854,129

10.56
Non-exercisable options vest annually over periods ranging from one to three years.
The estimated fair value of stock options granted during the period was determined using the Black-Scholes valuation model using the following weighted average assumptions:
 
2019
2018
Risk-free interest rate
1.52%
1.89%
Expected hold period to exercise
3.0 years
3.0 years
Expected share price volatility
74.02%
83.94%
Expected forfeiture rate
3.67%
3.67%
Expected dividend yield
Nil
Nil
Weighted average fair value of options
$1.04
$4.03

We use historical data to estimate the expected dividend yield and expected volatility of our stock in determining the fair value of the stock options. The risk-free interest rate is based on the Government of Canada benchmark bond yield rates in effect at the time of grant and the expected life of the options represents the estimated length of time the options are expected to remain outstanding.

12


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Incentive Share Award Plan
Restricted Share Units
We have issued restricted share units ("RSUs") to non-employee directors through our incentive share award plan. Grants of RSUs to non-employee directors vest either immediately, on the third anniversary date from the grant date or when the director ceases to be a member of the board. We have also issued RSUs to certain officers and employees of the Company. Grants of RSUs to certain officers and employees of the Company vest over a three year period. The following RSUs are outstanding at September 30:
 
2019
2018
Outstanding, beginning of the period
260,755

190,407

Granted during the period
45,963

8,891

Forfeited during the period

(2,105
)
Vested during the period
(55,176
)

Outstanding, end of the period
251,542

197,193

(1)The weighted average fair value of the RSUs granted was $1.42 in 2019 (2018 - $6.27).
Performance Share Units
We have also issued performance share units ("PSUs") to certain officers and employees of the Company. Grants of PSUs require completion of certain performance criteria and cliff vest after 3 years or vest over a three year period, depending on the grant. PSU grants to certain officers will vest immediately upon a change of control of the Company. If certain officers cease employment with the Company, vesting occurs on a pro rata basis prior to the third anniversary of the grant but after the first anniversary. The following PSUs are outstanding at September 30:
 
2019
2018
Outstanding, beginning of the period
63,156

94,734

Forfeited during the period

(31,578
)
Vested during the period
(2,105
)

Outstanding, end of the period
61,051

63,156


We have reserved 2,503,992 common shares for issuance relating to our outstanding equity compensation plans. Compensation expense related to stock options, RSUs and PSUs was $250,384 and $811,491 for the three and nine month periods ending September 30, 2019, respectively (September 30, 2018 - $236,607 and $932,817, respectively).

Note 8: Loss Per Common Share
 
Loss per common share is calculated using net loss for the year and the weighted average number of common shares outstanding for the three and nine month periods ended September 30, 2019 of 22,642,016 and 20,431,792, respectively (September 30, 2018 - 16,540,612 and 15,646,117, respectively). The effect of any potential exercise of our stock options and warrants outstanding during the year has been excluded from the calculation of diluted loss per common share, as it would be anti-dilutive.








13


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Note 9: Contract Liability

Regional licensing agreement
We entered into a regional licensing agreement (the "Licensing Agreement") with Adlai Nortye Biopharma Co., Ltd. ("Adlai") in November 2017. Under the terms of the Licensing Agreement, Adlai will have exclusive development and commercialization rights to pelareorep in China, Hong Kong, Macau, Singapore, South Korea and Taiwan. We are entitled to receive upfront license fees, development and regulatory milestone payments, royalties and sales-based milestone payments.

Warrant purchase agreement
We also entered into a warrant purchase agreement with Adlai. As at September 30, 2019, we were entitled to the following:
One common share purchase warrant of US$6 million whereby, upon exercise, Adlai may purchase our common shares priced at a 20% premium to the five-day weighted average closing price immediately preceding the exercise date. We have the right to call this warrant upon the enrollment of the 50th patient in the phase 3 metastatic breast cancer study.
This common share purchase warrant expires on November 14, 2020.

Contract liability
Our contract liability balance, which we expect to record in revenue over the next five years, is as follows:
 
September 30,
2019
$
December 31,
2018
$
Balance, beginning of the period
6,730,287

6,182,580

Regional licensing agreement

547,707

Revenue recognized in the period


Balance, end of the period
6,730,287

6,730,287

 
 
 
Contract liability - current

927,400

Contract liability - non-current
6,730,287

5,802,887

 
6,730,287

6,730,287


Note 10: Commitments
 
We are committed to payments totaling $5,599,483 for activities related to our clinical trial, manufacturing and collaboration programs which are expected to occur over the next two years.

Our commitments include one-half of the committed payments related to our collaboration with Merck KGaA, Darmstadt, Germany, and Pfizer Inc, known as BRACELET-1 (BReast cAnCEr with the Oncolytic Reovirus PeLareorEp in CombinaTion with anti-PD-L1 and Paclitaxel), as the cost of this phase 2 clinical trial will be shared equally between Oncolytics and Pfizer. As at September 30, 2019, we recorded $408,774 (December 31, 2018 - nil) in other receivables related to BRACELET-1 cost recovery from Pfizer.
 
Under a clinical trial agreement entered into with the Alberta Cancer Board (“ACB”), we have agreed to repay the amount funded under the agreement together with a royalty, to a combined maximum amount of $400,000 plus an overhead repayment of $100,000, upon sales of a specified product. We agreed to repay the ACB in annual installments in an amount equal to the lesser of: (a) 5% of gross sales of a specified product; or (b) $100,000 per annum once sales of a specified product commence.






14


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Note 11: Capital Disclosures
 
Our objective when managing capital is to maintain a strong statement of financial position. We achieve our objective by obtaining adequate cash resources to support planned activities which include the clinical trial program, product manufacturing, administrative costs and intellectual property expansion and protection. We include shareholders’ equity and cash and cash equivalents in the definition of capital.
 
September 30,
2019
$
December 31,
2018
$
Cash and cash equivalents
12,298,678

13,699,881

Shareholders’ equity
3,451,153

6,195,363


We do not have any debt other than trade accounts payable and lease liabilities, and we have potential contingent obligations relating to the completion of our research and development of pelareorep.

In managing our capital, we estimate our future cash requirements by preparing a budget and a multi-year plan annually for review and approval by our Board. The budget establishes the approved activities for the upcoming year and estimates the costs associated with these activities. The multi-year plan estimates future activity along with the potential cash requirements and is based on our assessment of our current clinical trial progress along with the expected results from the coming year’s activity. Budget to actual variances are prepared and reviewed by management and are presented quarterly to the Board.

Historically, funding for our plan is primarily managed through the issuance of additional common shares and common share purchase warrants that upon exercise are converted to common shares. Management regularly monitors the capital markets attempting to balance the timing of issuing additional equity with our progress through our clinical trial program, general market conditions, and the availability of capital. There are no assurances that funds will be made available to us when required.

On May 4, 2018, we renewed our short form base shelf prospectus (the "Base Shelf") that qualifies for distribution of up to $150,000,000 of common shares, subscription receipts, warrants, or units (the "Securities") in either Canada, the US or both. Under a Base Shelf, we may sell Securities to or through underwriters, dealers, placement agents or other intermediaries and also may sell Securities directly to purchasers or through agents, subject to obtaining any applicable exemption from registration requirements. The distribution of Securities may be effected from time to time in one or more transactions at a fixed price or prices, which may be subject to change, at market prices prevailing at the time of sale, or at prices related to such prevailing market prices to be negotiated with purchasers and as set forth in an accompanying Prospectus Supplement.

Renewing our Base Shelf provides us with additional flexibility when managing our cash resources as, under certain circumstances, it shortens the time period required to close a financing and is expected to increase the number of potential investors that may be prepared to invest in our company. Funds received as a result of using our Base Shelf would be used in line with our Board approved budget and multi-year plan. Our renewed Base Shelf will be effective until May 25, 2020.

Our Base Shelf allowed us to enter into our Common Stock Purchase Agreement in September 2018, our ATM equity offering sales agreement in October 2018 and our public offering in August 2019 (see Note 6). We will use these equity arrangements to assist us in achieving our capital objective. Each arrangement provides us with the opportunity to raise capital at our sole discretion providing us with the ability to better manage our cash resources.

We are not subject to externally imposed capital requirements and there have been no changes in how we define or manage our capital in 2019.






15


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Note 12: Financial Instruments
 
Our financial instruments consist of cash and cash equivalents, other receivables, accounts payable and warrant derivative. As at September 30, 2019, the carrying amount of our cash and cash equivalents, other receivables and accounts payable approximated their fair value. The fair value of our warrant derivative recognized on the consolidated statements of financial position is based on level 2 (significant observable inputs) as these warrants have not been listed on an exchange and therefore do not trade on an active market. As at September 30, 2019, the fair value of our warrant derivative was $1,774,210 (December 31, 2018 - nil).
  
Credit risk
Credit risk is the risk of financial loss if a counterparty to a financial instrument fails to meet its contractual obligations. We are exposed to credit risk on our cash and cash equivalents in the event of non-performance by counterparties, but we do not anticipate such non-performance. Our maximum exposure to credit risk at the end of the period is the carrying value of our cash and cash equivalents.

We mitigate our exposure to credit risk by maintaining our primary operating and investment bank accounts with Schedule I banks in Canada. For our foreign domiciled bank accounts, we use referrals or recommendations from our Canadian banks to open foreign bank accounts and these accounts are used solely for the purpose of settling accounts payable or payroll.

Interest rate risk
Interest rate risk is the risk that future cash flows of a financial instrument will fluctuate because of changes in market interest rates. We are exposed to interest rate risk through our cash and cash equivalents. We mitigate this risk through our investment policy that only allows investment of excess cash resources in investment grade vehicles while matching maturities with our operational requirements.
 
Fluctuations in market rates of interest do not have a significant impact on our results of operations due to the short term to maturity of the investments held.
 
Currency risk
Currency risk is the risk that future cash flows of a financial instrument will fluctuate because of changes in foreign exchange rates. In the normal course of our operations, we are exposed to currency risk from the purchase of goods and services primarily in the U.S., the U.K. and the European Union. In addition, we are exposed to currency risk to the extent cash is held in foreign currencies from either the purchase of foreign currencies or when we receive foreign currency proceeds from operating and financing activities. As well, we are exposed to currency risk related to our regional licensing agreement, receivables connected with our BRACELET-1 study, and warrant derivative. The impact of a $0.01 increase in the value of the U.S. dollar against the Canadian dollar would have decreased our net loss in 2019 by approximately $12,394.  The impact of a $0.10 increase in the value of the British pound against the Canadian dollar would have increased our net loss in 2019 by approximately $8,964. The impact of a $0.10 increase in the value of the Euro against the Canadian dollar would have increased our net loss in 2019 by approximately $27,532.
 
We mitigate our foreign exchange risk by maintaining sufficient foreign currencies, through the purchase of foreign currencies or receiving foreign currencies from financing activities, to settle our foreign accounts payable.

Balances in foreign currencies at September 30, 2019 are as follows:
 

US dollars
$

British pounds
£
Euro
Cash and cash equivalents
8,122,210
59,196
27,863
Other receivables
308,672
Accounts payable
(1,139,291)
(60,207)
(288,857)
Warrant derivative
(1,339,734)
 
5,951,857
(1,011)
(260,994)


16


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Liquidity risk
Liquidity risk is the risk that we will encounter difficulty in meeting obligations associated with financial liabilities. We manage liquidity risk through the management of our capital structure as outlined in Note 11. Accounts payable are all due within the current operating period.

Note 13: Additional Cash Flow Disclosures
 
Net Change In Non-Cash Working Capital
 
Three Month Period Ending September 30, 2019
$
Three Month Period Ending September 30, 2018
$
Nine Month Period Ending September 30, 2019
$
Nine Month Period Ending September 30, 2018
$
Change in:
 
 
 

 

Contract receivable



4,767,100

Other receivables
(413,908
)
32,819

(406,536
)
(19,169
)
Prepaid expenses
(657,069
)
39,182

(1,980,288
)
(273,967
)
Accounts payable and accrued liabilities
(368,715
)
(799,407
)
1,899,616

(1,486,992
)
Contract liability



547,707

Other liabilities

50,575

(39,338
)
50,575

Non-cash impact of foreign exchange
(51,454
)
80,052

114,373

45,737

Change in non-cash working capital related to operating activities
(1,491,146
)
(596,779
)
(412,173
)
3,630,991


Other Cash Flow Disclosures

Three Month Period Ending September 30, 2019
$
Three Month Period Ending September 30, 2018
$
Nine Month Period Ending September 30, 2019
$
Nine Month Period Ending September 30, 2018
$
Cash interest received
70,823

61,880

224,738

109,308

Cash taxes paid
1,085


5,461

3,752











17


ONCOLYTICS BIOTECH INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
September 30, 2019

Note 14: Other Expenses and Adjustments

We present our expenses based on the function of each expense and therefore include realized foreign exchange gains and losses, unrealized non-cash foreign exchange gains and losses and non-cash stock based compensation associated with research and development activity as a component of research and development expenses and depreciation of property and equipment, depreciation of right-of-use assets, non-cash stock based compensation associated with operating activities, and transactions costs related to our warrant derivative as a component of operating expenses.

Three Month Period Ending September 30, 2019
$
Three Month Period Ending September 30, 2018
$
Nine Month Period Ending September 30, 2019
$
Nine Month Period Ending September 30, 2018
$
Included in research and development expenses:








Realized foreign exchange loss (gain)
4,572

43,104

11,261

(4,401
)
Unrealized non-cash foreign exchange (gain) loss
(46,190
)
131,882

191,179

(105,114
)
Non-cash share based compensation
101,401

107,960

325,000

438,469










Included in operating expenses








Depreciation - property and equipment
24,483

26,698

98,190

67,682

Depreciation - right-of-use-assets
90,522


272,201


Non-cash share based compensation
148,983

128,647

486,491

494,348

Transaction costs, warrant derivative
233,143


233,143


Onerous lease contract

67,588


67,588

Amortization - lease incentive liability

12,494


12,494


Note 15: Related Party Transactions

Compensation of Key Management Personnel
Key management personnel are those persons having authority and responsibility for planning, directing and controlling our activities as a whole. We have determined that key management personnel consists of the members of the Board of Directors along with certain officers of the Company.

Three Month Period Ending September 30, 2019
$
Three Month Period Ending September 30, 2018
$
Nine Month Period Ending September 30, 2019
$
Nine Month Period Ending September 30, 2018
$
Short-term employee compensation and benefits
615,207

399,855

1,993,227

1,356,410

Share-based payments
220,055

185,643

723,856

672,325


835,262

585,498

2,717,083

2,028,735




18







ONCOLYTICSLOGOBLUEA06.JPG

MANAGEMENT DISCUSSION & ANALYSIS

September 30, 2019




November 12, 2019

MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

This discussion and analysis should be read in conjunction with the unaudited interim consolidated financial statements of Oncolytics Biotech® Inc. as at and for the three and nine months ended September 30, 2019 and 2018, and and should also be read in conjunction with the audited consolidated financial statements and Management's Discussion and Analysis of Financial Condition and Results of Operations (“MD&A”) contained in our annual report for the year ended December 31, 2018. The financial statements have been prepared in accordance with International Financial Reporting Standards ("IFRS").

FORWARD-LOOKING STATEMENTS

The following discussion contains forward-looking statements, within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended and under applicable Canadian provincial securities legislation. Forward-looking statements, including our belief as to the potential of pelareorep, an intravenously delivered immuno-oncolytic virus, as a cancer therapeutic and our expectations as to the success of our research and development, clinical and manufacturing programs in 2019 and beyond, future financial position, business strategy and plans for future operations, and statements that are not historical facts, involve known and unknown risks and uncertainties, which could cause our actual results to differ materially from those in the forward-looking statements.
Such risks and uncertainties include, among others, the need for and availability of funds and resources to pursue research and development projects, the efficacy of pelareorep as a cancer treatment, the success and timely completion of clinical studies and trials, our ability to successfully commercialize pelareorep, uncertainties related to the research, development and manufacturing of pelareorep, uncertainties related to competition, changes in technology, the regulatory process and general changes to the economic environment.
With respect to the forward-looking statements made within this MD&A, we have made numerous assumptions regarding among other things: our ability to obtain financing to fund our clinical development plan, our ability to receive regulatory approval to commence enrollment in the clinical studies which are part of our clinical development plan, our ability to maintain our supply of pelareorep and future expense levels being within our current expectations.
Investors should consult our quarterly and annual filings with the Canadian and US securities commissions for additional information on risks and uncertainties relating to the forward-looking statements. Forward-looking statements are based on assumptions, projections, estimates and expectations of management at the time such forward-looking statements are made, and such assumptions, projections, estimates and/or expectations could change or prove to be incorrect or inaccurate. Investors are cautioned against placing undue reliance on forward-looking statements. We do not undertake to update these forward-looking statements except as required by applicable law.
Pelareorep Development Update For 2019

Oncolytics Biotech Inc. is a Development Stage Company

Since our inception in April of 1998, Oncolytics Biotech Inc. has been a development stage company. We have focused our research and development efforts on the development of pelareorep, an intravenously delivered immuno-oncolytic virus (IOV) with the potential to treat a variety of cancers. We have not been profitable since our inception and expect to continue to incur substantial losses as we continue research and development efforts. We do not expect to generate significant revenues until, and unless, pelareorep becomes commercially viable.
Our goal each year is to advance pelareorep through the various steps and stages of development required for potential pharmaceutical products. In order to achieve this goal, we actively manage the development of our clinical trial program, our non-clinical and collaborative programs, our manufacturing process and pelareorep supply, and our intellectual property.



1



Clinical Trial Program

Our clinical development plan, based on drug combinations that can potentially boost the anti-tumor activities of pelareorep, has two main objectives:

The primary objective is to obtain regulatory approval as quickly as possible and is based on our compelling metastatic breast cancer (mBC) survival data presented at the 2017 AACR Annual Meeting. Using these survival data as the basis for our registration program, we may advance pelareorep directly into a phase 3 trial under a 2018 agreement with the United States Food and Drug Administration (FDA) under a Special Protocol Assessment (SPA). In an effort to increase the likelihood of success in the planned phase 3 program, we first have undertaken studies to define a biomarker that may allow us to more cost-effectively and more quickly enroll patients into the phase 3 trials and to populate the study with patients more likely to respond to therapy.

The second objective is to expand the commercial potential of pelareorep by testing its capacity to boost the effectiveness of valuable new treatments, including immunotherapies like checkpoint inhibitors.

Third Quarter 2019 Developments

Clinical studies aiding registration program

Collaboration with Merck KGaA, Darmstadt, Germany, and Pfizer Inc.: BRACELET-1 study
In June 2019, we entered into an agreement with Merck KGaA, Darmstadt, Germany and Pfizer Inc. to co-develop pelareorep in combination with paclitaxel and avelumab, a human anti-PD-L1 antibody, for the treatment of hormone-receptor positive, human epidermal growth factor 2-negative (HR+ / HER2-) mBC. The cost of this phase 2 clinical trial will be shared equally between Oncolytics and Pfizer. The study, known as BRACELET-1 (BReast cAnCEr with the Oncolytic Reovirus PeLareorEp in CombinaTion with anti-PD-L1 and Paclitaxel), is an open label study planned to enroll 45 patients into three cohorts with 15 patients per cohort: paclitaxel alone, paclitaxel in combination with pelareorep, and paclitaxel in combination with both pelareorep and avelumab. The study will examine the expression of immune-related biomarkers to identify changes in T cell population between pre-treatment and on-therapy biopsies to confirm our previously identified biomarker and is designed to assess efficacy in terms of overall response rate at week 16 per RECIST 1.1 and iRECIST. The safety of the combination will also be evaluated. Similar to the AWARE-1 study (see below), the results of this study may provide an opportunity to add an arm to our proposed phase 3 study that includes a checkpoint inhibitor in addition to the chemotherapy-virus combination. Furthermore, the results of the BRACELET-1 study will provide important confirmatory data in the same patient population where we presented compelling metastatic breast cancer survival data at the 2017 AACR Annual Meeting. These endpoints, including the biomarker data, are expected to further de-risk our planned phase 3 registration study, permitting for a smaller study with a higher likelihood of clinical success.

During the third quarter of 2019, we identified and negotiated with the cooperative group that will run the BRACELET-1 study. In October 2019, we announced our collaboration with PrECOG LLC, a leading cancer research network. The study is anticipated to begin enrollment in the first quarter of 2020.

Collaboration with SOLTI: AWARE-1 study
In September 2018, we announced a collaboration with SOLTI, an academic research group dedicated to clinical and translational research in breast cancer. This clinical collaboration, AWARE-1, is a window of opportunity study in the neoadjuvant setting for breast cancer using pelareorep in combination with F. Hoffmann-La Roche (Roche)'s anti-PD-L1 checkpoint inhibitor, atezolizumab (Tecentriq®), which we are utilizing under our Master Clinical Supply Agreement with Roche. The study plans to enroll 38 patients. Data generated from this study is intended to confirm that the virus is acting as a novel immunotherapy in breast cancer and to confirm biomarker data for breast cancer. The primary objective of this study is to supplement the existing randomized phase 2 results by providing key biomarker data points to enhance our probability of success in the phase 3 registration study. The results of this study may also provide an opportunity to add an arm to our proposed phase 3 study that includes a checkpoint inhibitor in addition to the chemotherapy-virus combination. In February 2019, we received approval for AWARE-1 from the Spanish Agency for Medicine and Health Products.

In July 2019, we announced preliminary AWARE-1 trial data demonstrating viral replication and promotion of inflammation following systemic administration of pelareorep when combined with Tecentriq®. Early data suggest a correlation between T cell population and viral replication with highly infected tumors. We have also received a favorable recommendation from the Steering Committee to advance into the next phase of the AWARE-1 study. We expect to announce additional interim data from the study before the end of 2019.

2



Additional checkpoint inhibitor combinations

Pancreatic cancer study combining pelareorep and Keytruda®  
In 2018, we announced the first patient had been treated in our investigator sponsored study (IST) supported by Merck Inc. (Merck), Northwestern University along with Oncolytics. This study, an extension of our phase 1 study (REO 024), will investigate pelareorep in combination with Merck’s anti-PD1 checkpoint inhibitor Keytruda®, to treat second line pancreatic cancer patients. The study plans to enroll approximately 40 patients.

During the third quarter of 2019, we continued patient enrollment and treatment.

Multiple myeloma study combining pelareorep and Opdivo®  
In 2018, we announced that the first patient had been treated in our IST with Emory University and the University of Utah investigating the combination of pelareorep and Bristol-Myers Squibb's anti-PD1 checkpoint inhibitor Opdivo® in 40 - 50 relapsed or refractory myeloma patients.

During the third quarter of 2019, we continued patient enrollment in the safety cohort investigating the combination of proteosome with the checkpoint inhibitor prior to the addition of pelareorep.

Post Q3 2019 Development

In October 2019, the following presentation was made on the results of a metanalysis of 13 clinical studies of pelareorep:
Title
Presenter
Location
Description/Conclusion
Systemic administration of oncolytic reovirus, pelareorep, a metanalysis on the efficiency of tumor delivery
Grey Wilkinson, PhD, Translational Scientist, Oncolytics Biotech Inc.
International Oncolytic Virus Conference (IOVC) 2019, Rochester, Minnesota
The analyses examined the effectiveness of viral replication within the tumors of patients treated systemically with pelareorep. The data demonstrated that, unlike other oncolytic viruses that require intra-tumoral delivery, intravenous (IV) systemic delivery of pelareorep resulted in 81% of patient tumor samples across multiple types of cancer testing positive for virus replication, with no infection in normal tissue. These results are from studies across a broad range of solid and liquid tumors, including metastatic disease.

Key Findings from the Metanalysis:
After IV delivery, 81% of patient tumor samples are positive for replicating reovirus (the average increases to 96% when melanoma and skin biopsies are excluded)
Tumor types that showed a high proportion of active viral replication: breast cancer, pancreatic adenocarcinoma, multiple myeloma, colorectal cancer patients with liver metastases and high-grade glioma

In November 2019, the following presentation was made on the data from the AWARE-1 study:
Title
Presenter
Location
Description/Conclusion
A window-of-opportunity Study of pelareorep in Early Breast Cancer (AWARE-1)
Aleix Prat, MD, PhD, et al., Head, Medical Oncology Department, Hospital Clinic of Barcelona & Associate Professor, University of Barcelona, SOLTI - Breast Cancer Research Group
The Society for Immunotherapy of Cancer (SITC) 2019, National Harbor, Maryland
The primary objective of this study is to evaluate changes in the immune environment of patients diagnosed with breast cancer. Importantly, an increase in CelTIL score, which means a change or expansion of infiltrating immune cells, known to correlate with a positive patient outcome. 

Initial data indicate viral replication exclusively in breast cancer tumor tissue and an increase in CelTIL score through the expansion of existing T cells and the creation of new T cell clones.





3



Manufacturing and Process Development

During the third quarter of 2019, as we continued our production of 100-litre cGMP batches, we supplied our clinical development program with previously filled product from our existing stock of pelareorep, labeled for the applicable usage. As well, we continued our activities to develop clinical and commercial production capabilities to fill pelareorep into vials, the next step in the process validation master plan. Process validation is required to ensure that the resulting product meets required specifications and quality standards and will form part of the Company’s submission to regulators, including the FDA, for product approval.

Intellectual Property

At the end of the third quarter of 2019, we had been issued over 399 patents including 48 US and 21 Canadian patents as well as issuances in other jurisdictions. We have an extensive patent portfolio covering the oncolytic reovirus that we use in our clinical trial program including a composition of matter patent that expires in 2028. Our patent portfolio also includes methods for treating proliferative disorders using modified adenovirus, HSV, parapoxvirus and vaccinia virus.

Financing Activity

U.S. "at-the-market" equity distribution agreement
During the three month period ending September 30, 2019, we sold 28,916 common shares for gross proceeds of US$46,306. We incurred share issue costs of $5,859.

Public offering
On August 16, 2019, pursuant to an underwritten public offering, 4,619,773 units were sold at a purchase price of US$0.81 per unit for gross proceeds of US$3,742,016. Each unit included one common share with a fair value of US$0.54 and one common share purchase warrant with a fair value of US$0.27 (see Note 5 and 6 of our interim consolidated financial statements). Each common share purchase warrant entitles the holder to purchase one common share at an exercise price of US$0.90 until August 16, 2024. We incurred transaction costs of $699,427 of which $466,284 were allocated to share issue costs and $233,143 were allocated to operating expenses, based on their relative fair values.

Financial Impact

We estimated at the beginning of the second quarter of 2019 that our cash requirements to fund our operations for the year will be between $19 - $20 million. We now expect our cash requirement for 2019 to be between $18 - $20 million, depending on our ultimate clinical program. Our cash usage for the nine month period ending September 30, 2019 was $12,651,215 for operating activities and $9,660 for the acquisition of property and equipment. Our net loss for the period was $13,721,246.

Cash Resources

We exited the third quarter of 2019 with cash and cash equivalents totaling $12,298,678 (see “Liquidity and Capital Resources”).

Pelareorep Development for the Remainder of 2019

Our planned 2019 development activity for pelareorep focuses on our clinical development plan along with our manufacturing and intellectual property programs. Our 2019 clinical objective is to incorporate our immuno-oncology combination strategy that includes checkpoint inhibitors and confirming the existence of a biomarker as we finalize our registration strategy and clinical protocol in preparation for a phase 3 clinical study in mBC. Before the end of 2019, we expect to continue enrollment in our AWARE-1, REO 024 extension and Opdivo® combination studies. We also expect to announce additional interim data from the AWARE-1 study. With respect to BRACELET-1, we expect to complete regulatory filings and commence clinical trial site selection and initiation activities by the first quarter of 2020 with patient enrollment anticipated to begin in the first quarter of 2020. Our expectation is that these combination studies will assist us in refining our phase 3 protocol for mBC and may also support further development around the innate and adaptive immunity components of the mechanism of action.

Our 2019 manufacturing program includes preparation for continued production of 100-litre cGMP batches along with the related analytical testing and product filling, as well as labeling, packaging and shipping of pelareorep to our various clinical sites for ongoing and upcoming activities. These actions also contribute to progression through our process validation master plan. Finally,

4



our intellectual property program includes filings for additional patents along with monitoring activities required to protect our patent portfolio.

We currently estimate the cash requirements to fund our operations for 2019 will be approximately $18 - $20 million, but will depend on our ultimate clinical program (see “Liquidity and Capital Resources”).

Third Quarter Results of Operations
(for the three months ended September 30, 2019 and 2018)

Net loss for the three month period ended September 30, 2019 was $3,528,644 compared to $3,335,866 for the three month period ended September 30, 2018.

Research and Development Expenses (“R&D”)
 
2019
$
2018
$
Clinical trial expenses
337,134

465,634

Manufacturing and related process development expenses
361,476

352,506

Intellectual property expenses
153,507

224,030

Research collaboration expenses
31,742

40,888

Other R&D expenses
674,484

563,401

Foreign exchange gain
(41,618
)
174,986

Share based payments
101,401

107,960

Research and development expenses
1,618,126

1,929,405


Clinical Trial Expenses
 
2019
$
2018
$
Clinical trial expenses
337,134

465,634


Our clinical trial expenses for the third quarter of 2019 were $337,134 compared to $465,634 for the third quarter of 2018. In the third quarter of 2019, our costs relating to the preparation and development of our breast cancer registration study included patient enrollment and treatment for our AWARE-1 study and study initiation activities for our BRACELET-1 study. In addition to activities related to our breast cancer program, we also incurred close out costs related to our fully enrolled legacy clinical trials and costs related to patient enrollment and/or treatment in our checkpoint inhibitor pancreatic cancer study investigating Keytruda® in combination with pelareorep.

In the third quarter of 2018, our clinical activities mainly related to closing out certain fully enrolled clinical trials and the migration and conversion of our safety data. We also incurred expenses related to updating our supporting regulatory documents and regulatory consulting activities connected to our combination studies.

Manufacturing & Related Process Development Expenses (“M&P”)
 
2019
$
2018
$
Product manufacturing expenses
313,489

193,159

Process development expenses
47,987

159,347

Manufacturing and related process development expenses
361,476

352,506


Our M&P expenses for the third quarter of 2019 were $361,476 compared to $352,506 for the third quarter of 2018. During the third quarter of 2019, our product manufacturing costs primarily related to shipping and storage costs of our bulk and vialed product and production run testing. During the third quarter of 2018, our product manufacturing costs included shipping and storage costs of our bulk and vialed product along with relabeling activities in line with extended stability data.


5



Our process development expenses for the third quarter of 2019 focused on analytical development and for the third quarter of 2018 focused on analytical development and transfer and stability studies

Intellectual Property Expenses
 
2019
$
2018
$
Intellectual property expenses
153,507

224,030


Our intellectual property expenses for the third quarter of 2019 were $153,507 compared to $224,030 for the third quarter of 2018. The change in intellectual property expenditures reflects the timing of filing costs associated with our patent base. At the end of the third quarter of 2019, we had been issued over 399 patents including 48 US and 21 Canadian patents, as well as issuances in other jurisdictions.

Research Collaboration Expenses
 
2019
$
2018
$
Research collaboration expenses
31,742

40,888


Our research collaboration expenses were $31,742 for the third quarter of 2019 compared to $40,888 for the third quarter of 2018. Our research collaborations during the third quarter of 2019 and 2018 included studies investigating the interaction of the immune system and pelareorep. Our research collaborations during the third quarter of 2018 also included biomarker studies.

Other Research and Development Expenses
 
2019
$
2018
$
R&D salaries and benefits
637,671

520,492

Other R&D expenses
36,813

42,909

Other Research and Development expenses
674,484

563,401


Our Other Research and Development expenses were $674,484 for the third quarter of 2019 compared to $563,401 for the third quarter of 2018. The change in our R&D salaries and benefits was mainly due to the timing of filling open positions in our U.S. office. Our Other R&D in the third quarter of 2019 expenses remained consistent with the third quarter of 2018.

Foreign Exchange (Gain) Loss
 
2019
$
2018
$
Foreign exchange (gain) loss
(41,618
)
174,986


Our foreign exchange gain was $41,618 for the third quarter of 2019 compared to a loss of $174,986 for the third quarter of 2018. The foreign exchange gain incurred in the third quarter of 2019 was primarily due to unrealized translation gain on U.S dollar denominated cash balances, partly offset by unrealized translation loss on U.S. denominated accounts payable. The foreign exchange loss incurred in the third quarter of 2018 was primarily due to the fluctuation in the U.S. dollar exchange rate on the translation of U.S. currency received from our June 2018 public offering and the settlement of our contract receivable.

Share Based Payments
 
2019
$
2018
$
Share based payments
101,401

107,960


Non-cash share based payment expenses for the third quarter of 2019 were $101,401 compared to $107,960 for the third quarter of 2018. We incurred share based payment expenses associated with the vesting of granted options and share awards to officers and employees.


6



Operating Expenses
 
2019
$
2018
$
Public company related expenses
933,858

488,018

Office expenses
636,175

824,899

Depreciation - property and equipment
24,483

26,698

Depreciation - right-of-use assets
90,522


Share based payments
148,983

128,647

Operating expenses
1,834,021

1,468,262


Our operating expenses for the third quarter of 2019 were $1,834,021 compared to $1,468,262 for the third quarter of 2018. Public company related expenses include costs associated with investor relations, business development and financial advisory activities, legal and accounting fees, corporate insurance, director fees and transfer agent and other fees relating to our Canadian and U.S. stock listings. Our public company related expenses were $933,858 for the third quarter of 2019 compared to $488,018 for the third quarter of 2018. The change in our public company related expenses in the third quarter of 2019 was due to transaction costs of $233,143 related to our August 2019 public offering (see Note 6 of our interim consolidated financial statements), an increase in investor relations and business development activities and the associated travel expenses, as well as an increase in insurance premiums.

Office expenses include compensation costs (excluding share based payments), rent related to short term leases and other office related costs. During the third quarter of 2019, our office expenses were $636,175 compared to $824,899 for the third quarter of 2018. The change was primarily due to a reduction in office rent expense following the adoption of IFRS 16 with an increase in depreciation of the newly created right-of-use assets (see Note 3 of our interim consolidated financial statements).

Non-cash share based payment expenses in the third quarter of 2019 were $148,983 compared to $128,647 in the third quarter of 2018. We incurred share based payment expenses associated with the vesting of granted options and share awards to officers, employees and non-employee directors.

Results of Operations
(for the nine month period ending September 30, 2019 and 2018)

Net loss for the nine month period ending September 30, 2019 was $13,721,246 compared to $12,217,979 for the nine month period ending September 30, 2018.

Research and Development Expenses (“R&D”)
 
2019
$
2018
$
Clinical trial expenses
1,608,186

2,311,934

Manufacturing and related process development expenses
3,302,211

1,211,275

Intellectual property expenditures
759,339

814,257

Research collaboration expenses
102,575

268,616

Other R&D expenses
2,024,243

1,974,677

Foreign exchange gain
202,440

(109,515
)
Share based payments
325,000

438,469

Research and development expenses
8,323,994

6,909,713









7



Clinical Trial Program
 
2019
$
2018
$
Clinical trial expenses
1,608,186

2,311,934


Our clinical trial expenses were $1,608,186 for the nine month period ending September 30, 2019 compared to $2,311,934 for the nine month period ending September 30, 2018. Our clinical trial activities related primarily to the preparation and development of our breast cancer registration program. During the nine month period ending September 30, 2019, these costs included startup activities and patient enrollment and treatment for our AWARE-1 study as well as costs to complete our supporting regulatory documents and key opinion leader activities. During the nine month period ending September 30, 2018, these costs included phase 3 development activities and activities related to obtaining the Special Protocol Assessment from the FDA.

During the nine month period ending September 30, 2019 and September 30, 2018, in addition to activities related to our breast cancer program, we also incurred close out costs related to our fully enrolled legacy clinical trials, patient enrollment and/or treatment in our checkpoint inhibitor pancreatic cancer study investigating Keytruda® in combination with pelareorep, and expenses related to updating our supporting regulatory documents.

We still expect our clinical trial expenses to increase in 2019 compared to 2018. For the remainder of 2019, we expect to generate clinical data with checkpoint inhibitors, confirm the existence of a biomarker and commence study initiation activities related to BRACELET-1.

Manufacturing & Related Process Development (“M&P”)
 
2019
$
2018
$
Product manufacturing expenses
3,142,323

830,471

Process development expenses
159,888

380,804

Manufacturing and related process development expenses
3,302,211

1,211,275


Our M&P expenses for the nine month period ending September 30, 2019 were $3,302,211 compared to $1,211,275 for the nine month period ending September 30, 2018. During the nine month period ending September 30, 2019, our product manufacturing costs primarily related to the completion of training and engineering production runs as well as shipping and storage costs of our bulk and vialed product. During the nine month period ending September 30, 2018, our product manufacturing costs included shipping and storage costs of our bulk and vialed product along with startup costs for a product fill required to support our clinical development plan. We also incurred costs related to relabeling activities in line with extended stability data.

Our process development expenses for the nine month period ending September 30, 2019 were $159,888 compared to $380,804 for the nine month period ending September 30, 2018. During the nine month period ending September 30, 2019, our process development activities focused on analytic development studies. During the nine month period ending September 30, 2018, our activities focused on analytic development and stability studies.

We still expect our M&P expenses for 2019 to increase compared to 2018. For the remainder of 2019, we expect to fill, label and store sufficient product as well as continue to perform analytical development and other non-clinical projects to support our clinical development program and other collaborative requirements.

Intellectual Property Expenses
 
2019
$
2018
$
Intellectual property expenses
759,339

814,257


Our intellectual property expenses for the nine month period ending September 30, 2019 were $759,339 compared to $814,257 for the nine month period ending September 30, 2018. The change in intellectual property expenditures reflects the timing of filing costs associated with our patent base. At the end of the nine month period ending September 30, 2019, we had been issued over 399 patents including 48 U.S. and 21 Canadian patents, as well as issuances in other jurisdictions.

8



We still expect that our intellectual property expenses will remain consistent in 2019 compared to 2018.

Research Collaborations
 
2019
$
2018
$
Research collaborations
102,575

268,616


Our research collaboration expenses for the nine month period ending September 30, 2019 were $102,575 compared to $268,616 for the nine month period ending September 30, 2018. During the nine month periods ending September 30, 2019 and 2018, our research collaborations included studies investigating the interaction of the immune system and pelareorep. Our research collaborations during the nine month period ending September 30, 2018 also included biomarker studies.
 
We now expect our research collaboration expenses for 2019 to decrease compared to 2018. We expect to complete our ongoing collaborative program and will continue to be selective in the types of new collaborations we enter into in 2019.

Other Research and Development Expenses
 
2019
$
2018
$
R&D salaries and benefits
1,876,695

1,821,362

Other R&D expenses
147,548

153,315

Other Research and Development expenses
2,024,243

1,974,677


Our Other Research and Development expenses for the nine month period ending September 30, 2019 were $2,024,243 compared to $1,974,677 for the nine month period ending September 30, 2018. The change in our R&D salaries and benefits was mainly due to the timing of filling open positions in our U.S. office. Our Other R&D expenses for nine month period ending September 30, 2019 remained consistent with the nine month period ending September 30, 2018.

We still expect our Other R&D expenses will remain consistent in 2019 compared to 2018.

Foreign Exchange Loss (Gain)
 
2019
$
2018
$
Foreign exchange loss (gain)
202,440

(109,515
)

Our foreign exchange loss for the nine month period ending September 30, 2019 was $202,440 compared to a gain of $109,515 for the nine month period ending September 30, 2018. The foreign exchange loss incurred during the nine month period ending September 30, 2019 was primarily due to unrealized translation loss on U.S dollar denominated cash balances, partly offset by unrealized translation gain on U.S. denominated accounts payable. The foreign exchange gain incurred during the nine month period ending September 30, 2018 was primarily due to unrealized translation gain on U.S. dollar denominated cash balances.

Share Based Payments
 
2019
$
2018
$
Share based payments
325,000

438,469


During the nine month period ending September 30, 2019, our non-cash share based payment expenses were $325,000 compared to $438,469 for the nine month period ending September 30, 2018. We incurred share based payment expenses associated with the vesting of granted options and share awards to officers and employees. In the second quarter of 2018, we also recognized a recovery of share based payment expenses due to the departure of the former Chief Medical Officer and the forfeiture of unvested share awards and options.


9



Operating Expenses
 
2019
$
2018
$
Public company related expenses
2,499,783

2,072,598

Office expenses
2,069,428

2,234,989

Depreciation - property and equipment
98,190

67,682

Depreciation - right-of-use assets
272,201


Share based payments
486,491

494,348

Operating expenses
5,426,093

4,869,617


Our operating expenses for the nine month period ending September 30, 2019 were $5,426,093 compared to $4,869,617 for the nine month period ending September 30, 2018. Public company related expenses include costs associated with investor relations, business development and financial advisory activities, legal and accounting fees, corporate insurance, director fees and transfer agent and other fees relating to our U.S. and Canadian stock listings. During the nine month period ending September 30, 2019, our public company related expenses were $2,499,783 compared to $2,072,598 for the nine month period ending September 30, 2018. The change was due to increased investor relations and business development activities, transaction costs of $233,143 related to our August 2019 public offering (see Note 6 of our interim consolidated financial statements), as well as increased insurance premiums. This is partly offset by lower professional fees, including legal fees and costs related to the special meeting of shareholders held in February 2018.

Office expenses include compensation costs (excluding share based payments), rent related to short term leases, and other office related costs. During the nine month period ending September 30, 2019, we incurred office expenses of $2,069,428 compared to $2,234,989 during the nine month period ending September 30, 2018. The change was due to a reduction in office rent expense following the adoption of IFRS 16 with an increase in depreciation of the newly created right-of-use assets (see Note 3 of our interim consolidated financial statements), partly offset by a change in salary levels and an increase in our U.S. headcount.

During the nine month period ending September 30, 2019, our non-cash share based payment expenses were $486,491 compared to $494,348 for the nine month period ending September 30, 2018. We incurred share based payment expenses associated with the vesting of granted options and share awards to officers, employees and non-employee directors.

We still expect our operating expenses to increase in 2019 compared to 2018. We expect to continue to grow our investor relations and business development activities and to continue to invest in our U.S. operations in support of our clinical development program. This increase is expected to be partly offset by a reduction in office rent expense following the adoption of IFRS 16 with an increase in depreciation of the newly created right-of-use assets (see Note 3 of our interim consolidated financial statements).
   
Commitments

As at September 30, 2019, we are committed to payments totaling approximately $5,599,483 for activities related to our clinical trial, manufacturing and collaboration programs which are expected to occur over the next two years. All of these committed payments are considered to be part of our normal course of business.

Our commitments include one-half of the committed payments related to our collaboration with Merck KGaA, Darmstadt, Germany, and Pfizer Inc, known as BRACELET-1, as the cost of this phase 2 clinical trial will be shared equally between Oncolytics and Pfizer. As at September 30, 2019, we recorded $408,774 (December 31, 2018 - nil) in other receivables related to BRACELET-1 cost recovery from Pfizer.








10



Summary of Quarterly Results

2019
2018
2017
 
Sept
June
Mar
Dec
Sept
June
Mar
Dec
Revenue








Net loss(1)
3,529

5,254

4,939

4,819

3,336

4,211

4,671

4,746

Basic and diluted loss per common share(1)
$
0.16

$
0.26

$
0.27

$
0.28

$
0.20

$
0.27

$
0.31

$
0.32

Total assets(2)
16,285

15,302

16,461

14,865

18,150

20,693

14,127

18,150

Total cash(2)
12,299

12,276

14,214

13,700

16,214

18,741

7,745

11,836

Total long-term debt








Cash dividends declared(3)
Nil

Nil

Nil

Nil

Nil

Nil

Nil

Nil

.
(1)
The calculation of basic and diluted loss per common share for all periods has been adjusted retrospectively for the share consolidation on May 22, 2018. Included in net loss and loss per common share between September 2019 and October 2017 are quarterly share based payment expenses of $250,384, $260,184, $300,923, $483,016, $236,607, $157,092, $539,118 and $140,659, respectively.
(2)
We issued 7,640,171 common shares and 4,619,773 share purchase warrants for net cash proceeds of $11.7 million in 2019 (2018 - 2,472,909 common shares for net cash proceeds of $13.3 million).
(3)
We have not declared or paid any dividends since incorporation.

Liquidity and Capital Resources

Share Consolidation
On May 22, 2018, we completed the consolidation of our common shares on the basis of 9.5 pre-consolidation common shares for each one post-consolidation common share. Fractional interests were rounded down to the nearest whole number of common shares. Outstanding stock options, restricted share units and performance share units were similarly adjusted by the consolidation ratio. Outstanding warrants were adjusted such that, following the Share Consolidation, 9.5 warrants issued in 2017 will entitle the holder to purchase one whole common share until June 1, 2022.

2019 Financing Activities

Common Stock Purchase Agreement
During the nine month period ending September 30, 2019, we sold 1,379,024 common shares for gross proceeds of US$2,663,768 and issued 11,348 commitment shares. The commitment shares have been valued at fair value of US$21,998 and have been recorded as share issue costs in addition to cash share issue costs of $3,757.

U.S. "at-the-market" equity distribution agreement
During the nine month period ending September 30, 2019, we sold 1,572,745 common shares for gross proceeds of US$3,030,892. We incurred share issue costs of $160,556.

Public offering
On August 16, 2019, pursuant to an underwritten public offering, 4,619,773 units were sold at a purchase price of US$0.81 per unit for gross proceeds of US$3,742,016. Each unit included one common share with a fair value of US$0.54 and one common share purchase warrant with a fair value of US$0.27 (see Note 5 and 6 of our interim consolidated financial statements). Each common share purchase warrant entitles the holder to purchase one common share at an exercise price of US$0.90 until August 16, 2024. We incurred transaction costs of $699,427 of which $466,284 were allocated to share issue costs and $233,143 were allocated to operating expenses, based on their relative fair values.

2018 Financing Activities

Listing on the Nasdaq Capital Market
On June 1, 2018, we announced that our common shares were approved for listing and commenced trading on the Nasdaq Capital Market.

Public offering
On June 5, 2018, we closed a public offering whereby we sold 1,532,278 post-consolidation common shares at a purchase price of US$5.83 per share for gross proceeds of US$8,933,181. We incurred share issue costs of $1,418,356.


11



Common Stock Purchase Agreement
On September 27, 2018, we entered into a Common Stock Purchase Agreement (the "Agreement") with Lincoln Park Capital Fund, LLC ("LPC") to sell up to US$26.0 million of common stock. Upon signing of the Agreement, LPC purchased 248,762 common shares for gross proceeds of US$1.0 million. We issued an initial commitment fee of 110,754 common shares to LPC valued at fair value of US$455,000. An additional 110,754 common shares will be issued on a pro rata basis under the terms of the Agreement as an additional commitment fee. We issued 4,260 additional commitment fee common shares valued at fair value of US$17,501. The initial commitment fee and additional commitment fee common shares were recorded as share issue costs in addition to cash share issue costs of $151,139.

Canadian "At-the-Market" equity distribution agreement
During the first quarter of 2018, we sold 519,500 pre-consolidation common shares (approximately 54,684 post-consolidation common shares) for net proceeds of $520,315.

Options
During the nine month period ending September 30, 2018, we received cash proceeds of $111,687 with respect to the exercise of 37,592 post-consolidation options (approximately 357,130 pre-consolidation options) by former employees.

Warrants
During the nine month period ending September 30, 2018, we received cash proceeds of $1,417 with respect to the exercise of 1,500 warrants.

Liquidity

As at September 30, 2019, we had cash and cash equivalents and working capital positions as follows:
 
September 30,
2019
$
December 31,
2018
$
Cash and cash equivalents
12,298,678

13,699,881

Working capital position
11,354,234

11,637,942


We do not have any debt other than trade accounts payable and lease liabilities, and we have potential contingent obligations relating to the completion of our research and development of pelareorep.

In managing our capital, we estimate our future cash requirements by preparing a budget and a multi-year plan annually for review and approval by our Board. The budget establishes the approved activities for the upcoming year and estimates the costs associated with these activities. The multi-year plan estimates future activity along with the potential cash requirements and is based on our assessment of our current clinical trial progress along with the expected results from the coming year’s activity.  Budget to actual variances are prepared and reviewed by management and are presented quarterly to the Board.

Historically, funding for our plan is primarily managed through the issuance of additional common shares and common share purchase warrants that upon exercise are converted to common shares. Management regularly monitors the capital markets attempting to balance the timing of issuing additional equity with our progress through our clinical trial program, general market conditions, and the availability of capital. There are no assurances that funds will be made available to us when required.

On May 4, 2018, we renewed our short form base shelf prospectus (the "Base Shelf") that qualifies for distribution of up to 150,000,000 of common shares, subscription receipts, warrants, or units (the "Securities") in either Canada, the US or both. Under a Base Shelf, we may sell Securities to or through underwriters, dealers, placement agents or other intermediaries and also may sell Securities directly to purchasers or through agents, subject to obtaining any applicable exemption from registration requirements. The distribution of Securities may be effected from time to time in one or more transactions at a fixed price or prices, which may be subject to change, at market prices prevailing at the time of sale, or at prices related to such prevailing market prices to be negotiated with purchasers and as set forth in an accompanying Prospectus Supplement.

Renewing our Base Shelf provides us with additional flexibility when managing our cash resources as, under certain circumstances, it shortens the time period required to close a financing and is expected to increase the number of potential investors that may be prepared to invest in our company. Funds received as a result of using our Base Shelf would be used in line with our Board approved budget and multi-year plan. Our renewed Base Shelf will be effective until May 25, 2020.


12



Our Base Shelf allowed us to enter into our Common Stock Purchase Agreement in September 2018, our ATM equity offering sales agreement in October 2018 and our public offering in August 2019 (see Note 6 of our interim consolidated financial statements). We will use these equity arrangements to assist us in achieving our capital objective. Each arrangement provides us with the opportunity to raise capital at our sole discretion providing us with the ability to better manage our cash resources.

We anticipate that the expected cash usage from our operations in 2019 will be between $18 - $20 million. We continue to manage our research and development plan with the objective of ensuring optimal use of our existing resources. Additional activities continue to be subject to adequate resources and we believe we will have sufficient cash resources to fund our presently planned operations to the end of 2019. Factors that will affect our anticipated cash usage in 2019, and for which additional funding might be required include, but are not limited to, expansion of our clinical trial program, the timing of patient enrollment in our approved clinical trials, the actual costs incurred to support each clinical trial, the number of treatments each patient will receive, the timing of R&D activity with our clinical trial research collaborations, the number, timing and costs of manufacturing runs required to conclude the validation process and supply product to our clinical trial program, and the level of collaborative activity undertaken.

We are not subject to externally imposed capital requirements and there have been no changes in how we define or manage our capital in 2019.

Financial Instruments and Other Instruments
Our financial instruments consist of cash and cash equivalents, other receivables, accounts payable and warrant derivative. As at September 30, 2019, the carrying amount of our cash and cash equivalents, other receivables and accounts payable approximated their fair value. In the third quarter of 2019, we issued common share purchase warrants with an exercise price denominated in a currency that differs from our functional currency, which were treated as a derivative measured at fair value with subsequent changes in fair value accounted for through the consolidated statement of loss (see Note 5 and 12 of our interim consolidated financial statements). As a result, we recorded a non-cash change in fair value of warrant derivative of $122,498 in the third quarter of 2019. The fair value of our warrant derivative recognized on the consolidated statements of financial position is based on level 2 (significant observable inputs) as these warrants have not been listed on an exchange and therefore do not trade on an active market. As at September 30, 2019, the fair value of our warrant derivative is $1,774,210 (December 31, 2018 - nil).
Credit risk
Credit risk is the risk of financial loss if a counter-party to a financial instrument fails to meet its contractual obligations. We are exposed to credit risk on our cash and cash equivalents in the event of non-performance by counterparties, but we do not anticipate such non-performance. Our maximum exposure to credit risk at the end of the period is the carrying value of our cash and cash equivalents.
We mitigate our exposure to credit risk by maintaining our primary operating and investment bank accounts with Schedule I banks in Canada. For our foreign domiciled bank accounts, we use referrals or recommendations from our Canadian banks to open foreign bank accounts and these accounts are used solely for the purpose of settling accounts payable or payroll.
Interest rate risk
Interest rate risk is the risk that future cash flows of a financial instrument will fluctuate because of changes in market interest rates. We are exposed to interest rate risk through our cash and cash equivalents. We mitigate this risk through our investment policy that only allows investment of excess cash resources in investment grade vehicles while matching maturities with our operational requirements.
Fluctuations in market rates of interest do not have a significant impact on our results of operations due to the short term to maturity of the investments held.
Currency risk
Currency risk is the risk that future cash flows of a financial instrument will fluctuate because of changes in foreign exchange rates. In the normal course of our operations, we are exposed to currency risk from the purchase of goods and services primarily in the U.S., the U.K. and the European Union. In addition, we are exposed to currency risk to the extent cash is held in foreign currencies from either the purchase of foreign currencies or when we receive foreign currency proceeds from operating and financing activities. As well, we are exposed to currency risk related to our regional licensing agreement, receivables connected with our BRACELET-1 study, and warrant derivative. The impact of a $0.01 increase in the value of the U.S. dollar against the Canadian dollar would have decreased our net loss in 2019 by approximately $12,394. The impact of a $0.10 increase in the value of the British pound against the Canadian dollar would have increased our net loss in 2019 by approximately $8,964. The impact of a $0.10 increase in the value of the Euro against the Canadian dollar would have increased our net loss in 2019 by approximately $27,532.

13



We mitigate our foreign exchange risk by maintaining sufficient foreign currencies, through the purchase of foreign currencies or receiving foreign currencies from financing activities, to settle our foreign accounts payable.
Balances in foreign currencies at September 30, 2019 are as follows:
 

US dollars
$

British pounds
£
Euro
Cash and cash equivalents
8,122,210
59,196
27,863
Other receivables
308,672
Accounts payable
(1,139,291)
(60,207)
(288,857)
Warrant derivative
(1,339,734)
 
5,951,857
(1,011)
(260,994)
Liquidity risk
Liquidity risk is the risk that we will encounter difficulty in meeting obligations associated with financial liabilities. We manage liquidity risk through the management of our capital structure as outlined in Note 11 of our interim consolidated financial statements. Accounts payable are all due within the current operating period.

Other MD&A Requirements

We have 26,357,724 common shares outstanding at November 8, 2019. If all of our options, restricted share units and performance share units (1,577,230), common share purchase warrants with a $9.025 exercise price (1,730,894) and common share purchase warrants with a US$0.90 exercise price (3,567,989), were exercised or were to vest, we would have 33,233,837 common shares outstanding.

Our 2018 annual report on Form 20-F is available on www.sedar.com.

Disclosure Controls and Procedures

There were no changes in our internal controls over financial reporting during the quarter ended September 30, 2019 that materially affected or are reasonably likely to materially affect, our internal controls over financial reporting.



14
FORM 52‑109F2
CERTIFICATION OF INTERIM FILINGS
FULL CERTIFICATE
I, Matthew Coffey, President and CEO of Oncolytics Biotech Inc., certify the following:
1.
Review: I have reviewed the interim financial report and interim MD&A (together, the “interim filings”) of Oncolytics Biotech Inc. (the “issuer”) for the interim period ended September 30, 2019.
2.
No misrepresentations: Based on my knowledge, having exercised reasonable diligence, the interim filings do not contain any untrue statement of a material fact or omit to state a material fact required to be stated or that is necessary to make a statement not misleading in light of the circumstances under which it was made, with respect to the period covered by the interim filings.
3.
Fair presentation: Based on my knowledge, having exercised reasonable diligence, the interim financial report together with the other financial information included in the interim filings fairly present in all material respects the financial condition, financial performance and cash flows of the issuer, as of the date of and for the periods presented in the interim filings.
4.
Responsibility: The issuer’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (DC&P) and internal control over financial reporting (ICFR), as those terms are defined in National Instrument 52‑109 Certification of Disclosure in Issuers’ Annual and Interim Filings, for the issuer.
5.
Design: Subject to the limitations, if any, described in paragraphs 5.2 and 5.3, the issuer’s other certifying officer(s) and I have, as at the end of the period covered by the interim filings:
(a)
designed DC&P, or caused it to be designed under our supervision, to provide reasonable assurance that:
(i)
material information relating to the issuer is made known to us by others, particularly during the period in which the interim filings are being prepared; and
(ii)
information required to be disclosed by the issuer in its annual filings, interim filings or other reports filed or submitted by it under securities legislation is recorded, processed, summarized and reported within the time periods specified in securities legislation; and
(b)
designed ICFR, or caused it to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with the issuer’s GAAP.
5.1
Control framework: The control framework the issuer’s other certifying officer and I used to design the issuer’s ICFR is the Internal Control -- Integrated Framework (2013) published by The Committee of Sponsoring Organizations of the Treadway Commission (COSO).



5.2
ICFR ‑ material weakness relating to design: N/A.
5.3
Limitation on scope of design: N/A.
6.
Reporting changes in ICFR: The issuer has disclosed in its interim MD&A any change in the issuer’s ICFR that occurred during the period beginning on January 1, 2019 and ended on September 30, 2019 that has materially affected, or is reasonably likely to materially affect, the issuer’s ICFR.
Date:     November 12, 2019    

/s/ Matthew Coffey
 
 
Matthew Coffey, PhD, MBA
 
 
President and CEO
 
 

 


FORM 52‑109F2
CERTIFICATION OF INTERIM FILINGS
FULL CERTIFICATE
I, Kirk Look, CFO of Oncolytics Biotech Inc., certify the following:
1.
Review: I have reviewed the interim financial report and interim MD&A (together, the “interim filings”) of Oncolytics Biotech Inc. (the “issuer”) for the interim period ended September 30, 2019.
2.
No misrepresentations: Based on my knowledge, having exercised reasonable diligence, the interim filings do not contain any untrue statement of a material fact or omit to state a material fact required to be stated or that is necessary to make a statement not misleading in light of the circumstances under which it was made, with respect to the period covered by the interim filings.
3.
Fair presentation: Based on my knowledge, having exercised reasonable diligence, the interim financial report together with the other financial information included in the interim filings fairly present in all material respects the financial condition, financial performance and cash flows of the issuer, as of the date of and for the periods presented in the interim filings.
4.
Responsibility: The issuer’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (DC&P) and internal control over financial reporting (ICFR), as those terms are defined in National Instrument 52‑109 Certification of Disclosure in Issuers’ Annual and Interim Filings, for the issuer.
5.
Design: Subject to the limitations, if any, described in paragraphs 5.2 and 5.3, the issuer’s other certifying officer(s) and I have, as at the end of the period covered by the interim filings:
(a)
designed DC&P, or caused it to be designed under our supervision, to provide reasonable assurance that:
(i)
material information relating to the issuer is made known to us by others, particularly during the period in which the interim filings are being prepared; and
(ii)
information required to be disclosed by the issuer in its annual filings, interim filings or other reports filed or submitted by it under securities legislation is recorded, processed, summarized and reported within the time periods specified in securities legislation; and
(b)
designed ICFR, or caused it to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with the issuer’s GAAP.
5.1
Control framework: The control framework the issuer’s other certifying officer and I used to design the issuer’s ICFR is the Internal Control -- Integrated Framework (2013) published by The Committee of Sponsoring Organizations of the Treadway Commission (COSO).



5.2
ICFR ‑ material weakness relating to design: N/A.
5.3
Limitation on scope of design: N/A.
6.
Reporting changes in ICFR: The issuer has disclosed in its interim MD&A any change in the issuer’s ICFR that occurred during the period beginning on January 1, 2019 and ended on September 30, 2019 that has materially affected, or is reasonably likely to materially affect, the issuer’s ICFR.
Date:     November 12, 2019    

/s/ Kirk Look
 
 
Kirk Look, CA
 
 
CFO