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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of report (Date of earliest event reported): December
17, 2024
ESSA Pharma Inc.
(Exact name of registrant as specified in its charter)
British Columbia, Canada
(State or other jurisdiction of incorporation) |
001-37410
(Commission File Number) |
98-1250703
(IRS Employer Identification No.) |
|
|
|
Suite 720, 999 West Broadway, Vancouver, British
Columbia, Canada
(Address of principal executive offices) |
V5Z 1K5
(Zip Code) |
Registrant’s telephone number, including area
code: (778) 331-0962
Check the appropriate box below if the Form 8-K filing is intended
to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
☐ Written communications pursuant to Rule 425 under the
Securities Act (17 CFR 230.425)
☐ Soliciting material pursuant to Rule 14a-12 under the
Exchange Act (17 CFR 240.14a-12)
☐ Pre-commencement communications pursuant to Rule 14d-2(b)
under the Exchange Act (17 CFR 240.14d-2(b))
☐ Pre-commencement communications pursuant to Rule 13e-4(c) under
the Exchange Act (17 CFR 240.13e-4(c))
Securities registered pursuant to Section 12(b) of the Act:
Title of
each class |
Trading
Symbol(s) |
Name of
each exchange on which registered |
Common Shares, no par value |
EPIX |
Nasdaq Capital Market |
Indicate by check mark whether the registrant is an emerging growth
company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange
Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant
has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant
to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
The following information is filed pursuant to Item
2.02, “Results of Operations and Financial Condition.”
On December 17, 2024, ESSA Pharma Inc. (the “Company”)
issued a press release announcing its financial results for the fiscal year ended September 30, 2024. A copy of the press release is attached
as Exhibit 99.1 to this Form 8-K.
The information provided under this Item (including
Exhibit 99.1) is intended to be furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange
Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated
by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific
reference in such filing.
Item 9.01 |
Financial Statements and Exhibits. |
|
|
|
(d) Exhibits |
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 hereunto duly authorized.
|
|
ESSA PHARMA INC.____________ |
|
|
(Registrant) |
Date: December 17, 2024 |
|
|
|
By: |
/s/ David Wood |
|
|
Name: David Wood |
|
|
Title: Chief Financial Officer |
Exhibit 99.1
ESSA Pharma Provides Corporate Update and Reports
Financial Results for Fiscal Fourth Quarter and Year Ended September 30, 2024
Company has initiated a process to explore and
review strategic options focused on maximizing shareholder value
SOUTH SAN FRANCISCO, California and VANCOUVER, Canada, Dec. 17,
2024 - ESSA Pharma Inc. (“ESSA,” or the “Company”) (NASDAQ: EPIX), a clinical-stage pharmaceutical company
that, prior to the discontinuation of its clinical trials and preclinical and other development programs, has been focused on developing
novel therapies for the treatment of prostate cancer, today provided a corporate update and reported financial results for the fourth
quarter and fiscal year ended September 30, 2024.
“We recently made the difficult decision to terminate the clinical
development of masofaniten, and withdraw the related IND and CTAs, based on an interim analysis of the data from the Phase 2 combination
study, concluding that masofaniten combined with enzalutamide was unlikely to meet its primary endpoint,” said David Parkinson,
MD, President and CEO of ESSA. “We are currently evaluating and reviewing our strategic options focused on maximizing shareholder
value and look forward to providing further updates in the near future.”
Fourth Quarter Fiscal 2024 and Recent Updates
| • | In October 2024, ESSA made the decision to terminate all clinical trials evaluating
masofaniten and to withdraw the related IND and CTAs. The decision was based on the outcome of a futility analysis conducted as part of
a protocol-specified interim review of the Phase 2 clinical trial evaluating masofaniten combined with enzalutamide versus enzalutamide
monotherapy in patients with metastatic castration-resistant prostate cancer (“mCRPC”) naïve to second-generation antiandrogens. |
| • | The interim analysis, which reviewed the Phase 2 safety, PK and efficacy data,
showed that the study enzalutamide monotherapy control arm (which is the standard of care for this patient population) had a much higher
rate of PSA90 response than was expected based upon historical data. In addition, there was no clear efficacy benefit seen with the combination
of masofaniten plus enzalutamide compared to enzalutamide single agent. A futility analysis determined a low likelihood of meeting the
prespecified primary endpoint of the study. It was therefore concluded that the study was unlikely to achieve its primary endpoint. |
| • | The combination of masofaniten plus enzalutamide was well-tolerated with no
new safety signals and a safety profile similar to that seen in Phase 1 monotherapy and combination studies. |
| • | ESSA has initiated a comprehensive process to explore and review a range of
strategic options focused on maximizing shareholder value, which may include, but are not limited to a merger, amalgamation, take-over,
business combination, asset sale or acquisition, shareholder distribution, wind-up, liquidation and dissolution, seek new products for
development, or other strategic direction. The process is expected to involve headcount and other cost reductions. |
| • | On December 12, 2024, ESSA provided a notice of termination of the License
Agreement to the Licensors, notifying the Licensors that it terminated the License Agreement in accordance with its terms, effective as
of December 12, 2024. |
Summary Financial Results
(Amounts expressed in U.S. dollars)
| • | Net Loss. ESSA recorded a net loss of $28.5 million for the year ended
September 30, 2024 compared to a net loss of $26.6 million for the year ended September 30, 2023. For the year ended September 30,
2024, this included non-cash share-based payments of $6.5 million compared to $5.3 million for the prior year, recognized for
stock options granted and vesting. Net loss for the fourth quarter ended September 30, 2024 was $6.4 million compared to a net loss of
$5.5 million for the fourth quarter ended September 30, 2023. |
| • | Research and Development (“R&D”) expenditures. R&D
expenditures for the year ended September 30, 2024 were $21.2 million compared to $21.3 million for the year ended September 30, 2023,
and include non-cash costs related to share-based payments ($1.8 million for the year ended 2024 compared to $2.7 million for
the year ended 2023). R&D expenditures for the fourth quarter ended September 30, 2024 were $4.2 million compared to $5.2 million
for the fourth quarter ended September 30, 2023 due to lower expenditures on preclinical and manufacturing. |
| • | General and Administration (“G&A”) expenditures. G&A
expenditures for the year ended September 30, 2024 were $13.2 million compared to $10.8 million for the year ended September 30, 2023,
and include non-cash costs related to share-based payments of $4.7 million for the year ended 2024 compared to $2.6 million
for the year ended 2023. G&A expenditures for the fourth quarter ended September 30, 2024 were $3.5 million compared
to $1.9 million for the fourth quarter ended September 30, 2023. The increase for the fourth quarter was primarily due
to increased share-based payments and higher salary figures. |
Liquidity and Outstanding Share Capital
| • | As of September 30, 2024, the Company had available cash reserves and short-term
investments of $126.8 million and net working capital of $124.3 million. The Company has no long-term debt facilities. |
| • | As of September 30, 2024, the Company had 44,388,550 common shares issued
and outstanding, and there were 2,920,000 common shares issuable upon the exercise of prefunded warrants at an exercise price of $0.0001.
|
About ESSA Pharma Inc.
ESSA is a clinical-stage pharmaceutical company that was previously
focused on developing novel and proprietary therapies for the treatment of patients with prostate cancer. For more information, please
visit www.essapharma.com.
Forward-Looking Statement Disclaimer
This release contains certain information which, as presented, constitutes
"forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995 and "forward-looking
information" within the meaning of applicable Canadian securities laws (collectively, "forward-looking statements"). Forward-looking
statements include, but are not limited to, statements that relate to future events and often addresses expected future business and financial
performance, containing words such as "anticipate", "believe", "plan", "estimate", "expect",
and "intend", statements that an action or event "may", "might", "could", "should",
or "will" be taken or occur, or other similar expressions and includes, but is not limited to, statements regarding the termination
of the Company's clinical studies of masofaniten, the Company's financial resources, the evaluation of the Company's strategic alternatives,
the primary and PSA-related endpoints of the Phase 2 study and other statements surrounding the Company's evaluation of masofaniten.
Forward-looking statements are subject to various known and unknown
risks and uncertainties, many of which are beyond the ability of ESSA to control or predict, and which may cause ESSA's actual results,
performance or achievements to be materially different from those expressed or implied thereby. Such statements reflect ESSA's current
views with respect to future events, are subject to risks and uncertainties and are necessarily based upon a number of estimates and assumptions
that, while considered reasonable by ESSA as of the date of such statements, are inherently subject to significant medical, scientific,
business, economic, competitive, political and social uncertainties and contingencies. In making forward looking statements, ESSA may
make various material assumptions, including but not limited to (i) the accuracy of ESSA's financial projections; (ii) obtaining positive
results of clinical trials; (iii) obtaining necessary regulatory approvals; (iv) that one or more strategic options may be available to
the Company at reasonably acceptable terms; and (v) general business, market and economic conditions.
Forward-looking statements are developed based on assumptions about
such risks, uncertainties and other factors set out herein and in ESSA's Annual Report on Form 10-K dated December [10], 2024, under the
heading "Risk Factors", a copy of which is available on ESSA's profile on EDGAR at www.sec.gov and on SEDAR+ at www.sedarplus.ca,
and as otherwise disclosed from time to time on ESSA's EDGAR and SEDAR+ profiles. Forward-looking statements are made based on management's
beliefs, estimates and opinions on the date that statements are made and ESSA undertakes no obligation to update forward-looking statements
if these beliefs, estimates and opinions or other circumstances should change, except as may be required by applicable United States and
Canadian securities laws. Readers are cautioned against attributing undue certainty to forward-looking statements.
Contacts
ESSA Pharma Inc.
David Wood, Chief Financial Officer
778.331.0962
dwood@essapharma.com
Investors and Media
Argot Partners
212.600.1902
essa@argotpartners.com
ESSA PHARMA INC.
CONSOLIDATED BALANCE SHEETS
Amounts in thousands of United States dollars
| |
September 30, 2024 | |
September 30, 2023 |
| |
| |
|
Cash | |
$ | 103,710 | | |
$ | 33,702 | |
Prepaids and other assets | |
| 24,402 | | |
| 115,420 | |
| |
| | | |
| | |
Total assets | |
$ | 128,112 | | |
$ | 149,122 | |
| |
| | | |
| | |
Current liabilities | |
| 3,301 | | |
| 3,495 | |
Long-term lease liability | |
| 205 | | |
| — | |
Shareholders' deficiency | |
| 124,606 | | |
| 145,627 | |
| |
| | | |
| | |
Total liabilities and shareholders' equity | |
$ | 128,112 | | |
$ | 149,122 | |
ESSA PHARMA INC.
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE
LOSS
Amounts in thousands of United States dollars, except
share and per share data
| |
Three months ended September 30, 2024 | |
Three months ended September 30, 2023 | |
Year ended September 30, 2024 | |
Year ended September 30, 2023 |
| |
| |
| |
| |
|
OPERATING EXPENSES | |
| | | |
| | | |
| | | |
| | |
Research and development | |
$ | 4,188 | | |
$ | 5,226 | | |
$ | 21,207 | | |
$ | 21,323 | |
Financing costs | |
| — | | |
| 1 | | |
| — | | |
| 7 | |
General and administration | |
| 3,507 | | |
| 1,922 | | |
| 13,214 | | |
| 10,812 | |
| |
| | | |
| | | |
| | | |
| | |
Total operating expenses | |
| (7,695 | ) | |
| (7,149 | ) | |
| (34,421 | ) | |
| (32,142 | ) |
| |
| | | |
| | | |
| | | |
| | |
Interest and other items | |
| 1,339 | | |
| 1,668 | | |
| 5,878 | | |
| 5,560 | |
| |
| | | |
| | | |
| | | |
| | |
Net loss before taxes | |
| (6,356 | ) | |
| (5,481 | ) | |
| (28,543 | ) | |
| (26,582 | ) |
Income tax expense (recovery) | |
| — | | |
| — | | |
| — | | |
| (2 | ) |
| |
| | | |
| | | |
| | | |
| | |
Net loss for the period | |
$ | (6,356 | ) | |
$ | (5,483 | ) | |
$ | (28,543 | ) | |
$ | (26,584 | ) |
| |
| | | |
| | | |
| | | |
| | |
OTHER COMPREHENSIVE LOSS | |
| | | |
| | | |
| | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Unrealized gain (loss) on short-term investments | |
| 37 | | |
| 2 | | |
| 57 | | |
| 15 | |
| |
| | | |
| | | |
| | | |
| | |
Loss and comprehensive loss for the period | |
$ | (6,319 | ) | |
$ | (5,479 | ) | |
$ | (28,486 | ) | |
$ | (26,569 | ) |
| |
| | | |
| | | |
| | | |
| | |
Basic and diluted loss per common share | |
$ | (0.14 | ) | |
$ | (0.12 | ) | |
$ | (0.64 | ) | |
$ | (0.60 | ) |
| |
| | | |
| | | |
| | | |
| | |
Weighted average number of common shares outstanding | |
| 44,366,126 | | |
| 44,092,374 | | |
| 44,277,050 | | |
| 44,089,557 | |
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