| Intangible assets |
Schedule of Intangible assets
| Cost |
|
Total |
|
| |
|
$ |
|
| Balance, December 31, 2019 |
|
|
378,814 |
|
| Additions |
|
|
46,588 |
|
| Impairment |
|
|
(100,220 |
) |
| Balance, December 31, 2020 |
|
|
325,182 |
|
| Additions |
|
|
39,809 |
|
| Balance, December 31, 2021 |
|
|
364,991 |
|
| Accumulated amortization |
|
Total |
|
| |
|
|
$ |
|
| Balance, December 31, 2019 |
|
|
106,426 |
|
| Amortization |
|
|
20,098 |
|
| Impairment |
|
|
(35,658 |
) |
| Balance, December 31, 2020 |
|
|
90,866 |
|
| Amortization |
|
|
17,882 |
|
| Balance, December 31, 2021 |
|
|
108,748 |
|
| Carrying values |
|
Total |
|
| |
|
|
$ |
|
| At December 31, 2020 |
|
|
234,316 |
|
| At December 31, 2021 |
|
|
256,243 |
|
The Company has licensed intellectual property
from various third parties. The intangible assets relate solely to licensed intellectual property and there are no other classes
of intangible assets. The intangible assets are as described below:
|
a) |
The Company has licensed from a third party (the “Licensor”), under patent rights purchase
agreement dated July 9, 2013 and amended April 15, 2014, certain patents relating to allopurinol for the treatment of hypertension.
The Company paid a total of $42,460 (US$40,000) to the Licensor per the terms of the agreement. |
The Company will also pay the
Licensor royalties on the cumulative net revenues from the sale or sublicense of the product covered under the patent license until
the later of (i) the expiration of the last patent right covering the product; and (ii) the expiration of ten years from the date
of the first commercial sales of a product.
|
b) |
In December 2012, the Company entered into an agreement to license certain intellectual property
relating to the use of all uric acid lowering agents to improve the treatment of metabolic syndrome. Under this patent rights purchase
agreement, between the Company and Dr. Richard Johnson and Dr. Takahiko Nakagawa (the “Vendors”), the Company issued
143,100 common shares at $0.35 per common share for a total instalment price of $50,400. The Company also had the option to pay
the Vendors an additional US$75,000 to purchase the patents which was set up as a provision in the year ended December 31, 2018. |
During the year ended December
31, 2020, the Company determined that it was no longer feasible to complete the purchase and as such, indicators of impairment
existed leading to a test of recoverable amount of the license, which resulted in an impairment loss of $64,562. As this valuation
technique requires management’s judgment and estimates of the recoverable amount, it is classified within level 3 of the
fair value hierarchy. During the year ended December 31, 2020, the purchase provision was reversed resulting in a gain of $95,490
on recovery of provision.
|
7. |
Intangible assets (continued) |
The Company will pay the Vendors
a royalty based on the cumulative net revenues from the sale or sublicense of the product covered under the licensed intellectual
property until the later of (i) the expiration of the last patent right covering the product; and (ii) the expiration of 10 years
from the date of the first commercial sales of a product.
|
c) |
Pursuant to a license agreement dated October 9, 2012, as amended on June 23, 2014, between the
Company and the University of Florida Research Foundation, Inc. (“UFRF”), the Company acquired the exclusive license
to certain intellectual property related to the use of all uric acid lowering agents to treat insulin resistance. The Company has
paid or is obligated to pay UFRF the following considerations: |
|
i) |
An annual license fee of US$1,000 (2021 fees - paid); |
|
ii) |
Reimburse UFRF for United States and/or foreign costs associated with the maintenance of the licensed
patents; |
|
iii) |
The issuance to UFRF of 180,397 shares of common stock of the Company (160,783 have been issued
to UFRF as at December 31, 2021. Remaining shares to be issued are included in obligation to issue shares); |
|
iv) |
Milestone payments of US$500,000 upon receipt of FDA approval to market licensed product in the
United States of America and US$100,000 upon receipt of regulatory approval to market each licensed product in each of other jurisdictions; |
|
v) |
Royalty payments of up to 1.5% of net sales of products covered by the license until the later
of (i) the expiration of any patent claims; or (ii) 10 years from the date of the first commercial sale of any covered product
in each country. Following commencement of commercial sales, the Company will be subject to certain annual minimum royalty payments
that will increase annually to a maximum of US$100,000 per year; and |
|
vi) |
UFRF is entitled to receive a royalty of 5% of amounts received from any sub-licensee that are
not based directly on product sales, excluding payments received for research and development or purchases of the Company’s
securities at not less than fair market value. |
UFRF may terminate the agreement if the Company fails
to meet the above specified milestones.
|