Portage Biotech Inc. (“Portage” or the “Company”) (NASDAQ: PRTG), a
clinical-stage immuno-oncology company with a portfolio of novel
multi-targeted therapies for use as monotherapy and in combination,
today announced its financial results for the fiscal year ended
March 31, 2024.
“After reviewing Portage’s funding requirements,
which necessitated discontinuing the clinical development of its
iNKT program and pausing patient enrollment in the ADPORT-601
clinical trial of PORT-6 (adenosine 2A inhibitor) and PORT-7
(adenosine 2B inhibitor), we continue to explore strategic
alternatives. These may include finding a partner for one or more
of our assets, a sale of our company, a merger, restructurings
(both in and out of court), a company wind down, further financing
efforts, or other strategic actions,” said Dr. Ian Walters, Chief
Executive Officer and Chairman of Portage.
Financial Results from Year Ended March 31,
2024
The Company incurred a net loss of approximately
$75.4 million during the fiscal year ended March 31, 2024 (“Fiscal
2024”), which includes approximately $60.6 million of net non-cash
expenses. This compares to a net loss of approximately $104.7
million during the fiscal year ended March 31, 2023 (“Fiscal
2023”), reflecting a decrease in net loss of $29.3 million
year-over-year. The decrease was primarily due to lower non-cash
losses on impairment related to the Company’s identifiable
intangible assets, goodwill, and certain investments and
convertible note receivable.
Operating expenses, which include research and
development (“R&D”) costs and general and administrative
(“G&A”) expenses, were $18.2 million in Fiscal 2024, compared
to $16.6 million in Fiscal 2023, an increase of $1.6 million. This
increase was primarily due to additional clinical development costs
related to the PORT-6 clinical trial and the iNKT clinical trial
for PORT-2, prior to discontinuing the Company’s iNKT trial and
pausing further enrollment in the ADPORT-601 clinical trial of
PORT-6 (adenosine 2A inhibitor) and PORT-7 (adenosine 2B
inhibitor).
R&D costs increased by approximately $3.8
million, or about 44%, from approximately $8.7 million in Fiscal
2023 to approximately $12.5 million in Fiscal 2024. The increase
was primarily attributable to clinical trial costs (principally
CRO-related), which increased by approximately $2.5 million, from
$2.7 million in Fiscal 2023 to $5.2 million in Fiscal 2024, as
activities ramped up until the Company decided to discontinue its
iNKT trial and pause patient enrollment in its ADPORT adenosine
trial in the third and fourth quarters of Fiscal 2024,
respectively. Manufacturing-related costs increased by $1.0
million, from $0.8 million in Fiscal 2023 to $1.8 million in Fiscal
2024, related to the iNKT and adenosine clinical trials.
Payroll-related expenses decreased by $0.3 million from $1.9
million in Fiscal 2023 to $1.6 million in Fiscal 2024; the
increases in salaries effective January 2023 were more than offset
by the fact that no annual bonuses were incurred in Fiscal 2024.
R&D non-cash share-based compensation expense decreased by $0.8
million, from $2.2 million in Fiscal 2023 to $1.4 million in Fiscal
2024. This decrease was due to the continued vesting of options
granted in prior years, as well as recent grants having a lower
grant date fair value. Additionally, in Fiscal 2024, the Company
incurred a milestone payment of $0.5 million for dosing its first
adenosine patient, an increase in consulting fees of approximately
$0.4 million from $0.4 million in Fiscal 2023 to $0.8 million in
Fiscal 2024 to reflect the increase in activity year-over-year, and
finally, $0.5 million in fees paid with respect to the transition
of the iNKT study, prior to discontinuing the study in Fiscal
2024.
G&A expenses decreased by approximately $2.2 million, or
about 28%, from approximately $7.9 million in Fiscal 2023 to
approximately $5.7 million in Fiscal 2024. Professional fees
decreased by $0.7 million, to $2.3 million in Fiscal 2024, compared
to $3.0 million in Fiscal 2023, primarily due to legal fees
associated with the Tarus acquisition and other regulatory filings
in Fiscal 2023. Additionally, G&A non-cash share-based
compensation expense decreased by $0.8 million, from $2.0 million
in Fiscal 2023 to $1.2 million in Fiscal 2024. This decrease was
attributable to the vesting of certain stock options granted in
prior years and the lower fair value of more recent grants.
Insurance expense decreased by $0.5 million, from $1.2 million in
Fiscal 2023 to $0.7 million in Fiscal 2024, due to a decrease in
the D&O premium year-over-year resulting from changes in the
insurance markets. Directors’ fees decreased by $0.1 million in
Fiscal 2024, compared to Fiscal 2023, as certain directors waived
their fees for the quarter ended March 31, 2024. Finally,
payroll-related expenses decreased by $0.1 million from $1.0
million in Fiscal 2023 to $0.9 million in Fiscal 2024; the increase
in annual salaries effectuated in January 2023 was slightly more
than offset by the fact that there were no annual bonuses incurred
in Fiscal 2024.
The Company’s other pre-tax items of income and expense were
substantially non-cash in nature, aggregating approximately $67.7
million in net expenses for Fiscal 2024, compared to approximately
$105.9 million in net expenses for Fiscal 2023. The net losses in
each year were attributed to impairments of intangible assets. The
impairment in Fiscal 2024 represented the full impairment of the
carrying value of in-process research and development of $57.9
million for iOx and $23.6 million for Tarus, as well as a $1.0
million loss on the impairment of the Company’s investment in
Stimunity and the Stimunity convertible note. These expenses were
partially offset by the non-cash gains from the decrease in the
fair value of the deferred purchase price payable to the former
Tarus shareholders and the deferred obligation for the iOx
milestone, totaling $11.3 million.
The Company recognized a $0.7 million gain on
the sale of Intensity shares, accounted for under fair value
through other comprehensive income (FVOCI), which had a carrying
value of $2.1 million and a $2.4 million loss during Fiscal 2024
from the Company’s equity financing in October 2023, representing
the excess of the fair value of certain warrants over the net
proceeds. Additionally, a $6.9 million non-cash gain was recognized
from the change in the fair value of certain warrants accounted for
as liabilities issued in connection with this equity offering.
Additionally, the Company recognized a non-cash
net deferred income tax benefit of $10.5 million in Fiscal 2024,
compared to a non-cash net deferred income tax benefit of $17.9
million in Fiscal 2023, a year-over-year change of $7.4 million.
This benefit was primarily attributable to the tax effect of the
non-cash impairment loss on IPR&D for iOx, partially offset by
the derecognition of previously recognized losses.
As of March 31, 2024, the Company had cash and
cash equivalents of approximately $5.0 million and total current
liabilities of approximately $2.9 million.
About Portage Biotech
Inc.
Portage is a clinical-stage immuno-oncology
company advancing multi-targeted therapies to extend survival and
significantly improve the lives of patients with cancer. The
Company has made the decision to discontinue its sponsored trial
for its the invariant natural killer T-cell (iNKT) program and
pause patient enrollment to its sponsored adenosine trial program
(ADPORT-601 trial) for its potentially best-in-class adenosine
antagonists PORT-6 (adenosine 2A inhibitor) and PORT-7 (adenosine
2B inhibitor). The Company is exploring strategic alternatives,
which may include finding a partner for one or more of its assets,
a sale of the company, a merger, restructurings, both in and out of
court, a company wind down, further financing efforts or other
strategic action. For more information, please visit
www.portagebiotech.com, follow us on Twitter at @PortageBiotech or
find us on LinkedIn at Portage Biotech Inc.
Forward-Looking Statements All
statements in this news release, other than statements of
historical facts, including without limitation, statements
regarding about the Company’s information that are forward-looking
in nature and, business strategy, plans and objectives of
management for future operations and those statements preceded by,
followed by or that otherwise include the words "believe,"
"expects," "anticipates," "intends," "estimates," “will,” “may,”
“plan,” “potential,” “continue,” or similar expressions or
variations on such expressions are forward-looking statements. For
example, statements regarding the Company's plans to continue
exploring strategic alternatives, which may include finding a
partner for one or more of its assets, a sale of the company, a
merger, restructurings (both in and out of court), a company wind
down, further financing efforts, or other strategic actions, are
forward-looking statements. As a result, forward-looking statements
are subject to certain risks and uncertainties, including, but are
not limited to: the Company's plans and ability to develop and
commercialize product candidates and the timing of these
development programs; the Company's clinical development of its
product candidates, including the results of current and future
clinical trials; the benefits and risks of the Company's product
candidates as compared to others; the Company's maintenance and
establishment of intellectual property rights in its product
candidates; the Company's ability to obtain financing in the future
to cover its operational costs and progress its plans for clinical
development, its estimates regarding its capital requirements, and
its ability to continue as a going concern; the Company’s estimates
of future revenues and profitability; the Company's estimates of
the size of the potential markets for its product candidates; its
selection and licensing of product candidates; and other factors
set forth in “Item 3 - Key Information-Risk Factors” in the
Company’s Annual Report on Form 20-F for the year ended March 31,
2024. Although the Company believes that the expectations reflected
in these forward-looking statements are reasonable, undue reliance
should not be placed on them as actual results may differ
materially from these forward-looking statements. The
forward-looking statements contained in this news release are made
as of the date hereof, and the Company undertakes no obligation to
update publicly or revise any forward-looking statements or
information, except as required by law.
FOR MORE INFORMATION, PLEASE CONTACT:Investor
Relations:ir@portagebiotech.com
Media Relations:media@portagebiotech.com
---tables to follow---
PORTAGE BIOTECH INC.Consolidated
Statements of Operations and Other Comprehensive Income
(Loss)(U.S. Dollars in thousands, except per share
amounts) |
|
|
|
|
Years Ended March 31, |
|
|
|
|
2024 |
|
|
2023 |
|
|
2022 |
|
Expenses |
|
|
|
|
|
|
|
|
|
|
Research and development |
|
$ |
12,535 |
|
$ |
8,674 |
|
$ |
6,769 |
|
General and administrative expenses |
|
|
5,664 |
|
|
7,901 |
|
|
8,819 |
|
Loss from
operations |
|
|
(18,199 |
) |
|
(16,575 |
) |
|
(15,588 |
) |
Change in fair value of deferred purchase price payable - Tarus and
deferred obligation - iOx milestone |
|
|
11,305 |
|
|
2,711 |
|
|
– |
|
Loss on Registered Direct Offering |
|
|
(2,432 |
) |
|
– |
|
|
– |
|
Offering costs |
|
|
(662 |
) |
|
– |
|
|
– |
|
Change in fair value of warrant liability |
|
|
6,868 |
|
|
33 |
|
|
852 |
|
Impairment loss - iOx IPR&D |
|
|
(57,890 |
) |
|
(59,320 |
) |
|
– |
|
Impairment loss - Tarus IPR&D |
|
|
(23,615 |
) |
|
(4,585 |
) |
|
– |
|
Impairment loss - Goodwill |
|
|
– |
|
|
(43,862 |
) |
|
– |
|
Impairment loss - Stimunity |
|
|
(1,002 |
) |
|
(818 |
) |
|
– |
|
Impairment loss - Saugatuck |
|
|
(178 |
) |
|
– |
|
|
– |
|
Commitment fee under Committed Purchase Agreement |
|
|
(839 |
) |
|
– |
|
|
– |
|
Share of loss in associate accounted for using equity method |
|
|
(233 |
) |
|
(260 |
) |
|
(62 |
) |
Gain on dissolution of investment in associate |
|
|
27 |
|
|
– |
|
|
– |
|
Gain from sale of investment in public company |
|
|
725 |
|
|
– |
|
|
– |
|
Foreign exchange transaction gain (loss) |
|
|
7 |
|
|
(53 |
) |
|
24 |
|
Depreciation expense |
|
|
(54 |
) |
|
(1 |
) |
|
– |
|
Interest income |
|
|
274 |
|
|
217 |
|
|
– |
|
Interest expense |
|
|
(32 |
) |
|
(9 |
) |
|
(43 |
) |
Loss before provision
for income taxes |
|
|
(85,930 |
) |
|
(122,522 |
) |
|
(14,817 |
) |
Income tax benefit (expense) |
|
|
10,548 |
|
|
17,856 |
|
|
(4,352 |
) |
Net loss |
|
|
(75,382 |
) |
|
(104,666 |
) |
|
(19,169 |
) |
Other comprehensive
income (loss) |
|
|
|
|
|
|
|
|
|
|
Net unrealized loss on investments |
|
|
(38 |
) |
|
(5,283 |
) |
|
– |
|
Total comprehensive
loss for year |
|
$ |
(75,420 |
) |
$ |
(109,949 |
) |
$ |
(19,169 |
) |
|
|
|
|
|
|
|
|
|
|
|
Net loss attributable
to: |
|
|
|
|
|
|
|
|
|
|
Owners of the Company |
|
$ |
(75,339 |
) |
$ |
(104,611 |
) |
$ |
(16,870 |
) |
Non-controlling interest |
|
|
(43 |
) |
|
(55 |
) |
|
(2,299 |
) |
Net loss |
|
$ |
(75,382 |
) |
$ |
(104,666 |
) |
$ |
(19,169 |
) |
|
|
|
|
|
|
|
|
|
|
|
Comprehensive loss
attributable to: |
|
|
|
|
|
|
|
|
|
|
Owners of the Company |
|
$ |
(75,377 |
) |
$ |
(109,894 |
) |
$ |
(16,870 |
) |
Non-controlling interest |
|
|
(43 |
) |
|
(55 |
) |
|
(2,299 |
) |
Total comprehensive
loss for year |
|
$ |
(75,420 |
) |
$ |
(109,949 |
) |
$ |
(19,169 |
) |
|
|
|
|
|
|
|
|
|
|
|
Loss per
share |
|
|
|
|
|
|
|
|
|
|
Basic and diluted |
|
$ |
(3.89 |
) |
$ |
(6.49 |
) |
$ |
(1.29 |
) |
|
|
|
|
|
|
|
|
|
|
|
Weighted average
shares outstanding |
|
|
|
|
|
|
|
|
|
|
Basic and diluted |
|
|
19,343 |
|
|
16,119 |
|
|
13,060 |
|
PORTAGE
BIOTECH INC.Consolidated Statements of Financial
Position(U.S. Dollars in thousands) |
|
|
|
March 31, |
|
|
|
2024 |
|
|
2023 |
|
Assets |
|
|
|
|
|
|
Current
assets |
|
|
|
|
|
|
Cash and cash equivalents |
|
$ |
5,028 |
|
|
$ |
10,545 |
|
Prepaid expenses and other receivables |
|
|
2,667 |
|
|
|
2,689 |
|
Convertible note receivable |
|
|
– |
|
|
|
442 |
|
Total current
assets |
|
|
7,695 |
|
|
|
13,676 |
|
Non-current
assets |
|
|
|
|
|
|
|
|
Investment in associate |
|
|
– |
|
|
|
806 |
|
Investment in public company |
|
|
– |
|
|
|
2,087 |
|
In-process research and development |
|
|
– |
|
|
|
81,683 |
|
Deferred commitment fee, net of amortization of $900 and $61,
respectively |
|
|
– |
|
|
|
839 |
|
Right to use asset |
|
|
35 |
|
|
|
– |
|
Other assets, including equipment, net |
|
|
49 |
|
|
|
38 |
|
Total non-current
assets |
|
|
84 |
|
|
|
85,453 |
|
Total
assets |
|
$ |
7,779 |
|
|
$ |
99,129 |
|
|
|
|
|
|
|
|
|
|
Liabilities and
Equity |
|
|
|
|
|
|
|
|
Current
liabilities |
|
|
|
|
|
|
|
|
Accounts payable and accrued liabilities |
|
$ |
2,836 |
|
|
$ |
1,865 |
|
Lease liability - current, including interest |
|
|
40 |
|
|
|
– |
|
Other current liabilities |
|
|
3 |
|
|
|
– |
|
Total current
liabilities |
|
|
2,879 |
|
|
|
1,865 |
|
Non-current
liabilities |
|
|
|
|
|
|
|
|
Lease liability - non-current |
|
|
7 |
|
|
|
– |
|
Warrant liability |
|
|
1,564 |
|
|
|
– |
|
Deferred tax liability |
|
|
– |
|
|
|
10,564 |
|
Deferred purchase price payable - Tarus |
|
|
– |
|
|
|
7,179 |
|
Deferred obligation - iOx milestone |
|
|
– |
|
|
|
4,126 |
|
Total non-current
liabilities |
|
|
1,571 |
|
|
|
21,869 |
|
Total
liabilities |
|
|
4,450 |
|
|
|
23,734 |
|
|
|
|
|
|
|
|
|
|
Shareholders’
Equity |
|
|
|
|
|
|
|
|
Capital stock |
|
|
219,499 |
|
|
|
218,782 |
|
Stock option reserve |
|
|
23,841 |
|
|
|
21,204 |
|
Accumulated other comprehensive loss |
|
|
– |
|
|
|
(4,325 |
) |
Accumulated deficit |
|
|
(239,318 |
) |
|
|
(159,616 |
) |
Total equity
attributable to owners of the Company |
|
|
4,022 |
|
|
|
76,045 |
|
Non-controlling
interest |
|
|
(693 |
) |
|
|
(650 |
) |
Total
equity |
|
|
3,329 |
|
|
|
75,395 |
|
Total liabilities and
equity |
|
$ |
7,779 |
|
|
$ |
99,129 |
|
Commitments and
Contingent Liabilities |
|
|
|
|
|
|
|
|
Portage Biotech (NASDAQ:PRTG)
過去 株価チャート
から 11 2024 まで 12 2024
Portage Biotech (NASDAQ:PRTG)
過去 株価チャート
から 12 2023 まで 12 2024