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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): March 8, 2024
ALLARITY THERAPEUTICS,
INC.
(Exact name of registrant
as specified in our charter)
Delaware |
|
001-41160 |
|
87-2147982 |
(State or other jurisdiction
of incorporation) |
|
(Commission File Number) |
|
(IRS Employer
Identification No.) |
24 School Street, 2nd Floor
Boston, MA |
|
02108 |
(Address of principal executive offices) |
|
(Zip Code) |
(401) 426-4664
(Registrant’s telephone
number, including area code)
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 Stock, par value $0.0001 per share |
|
ALLR |
|
The Nasdaq Stock Market LLC |
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.
On
March 8, 2024, Allarity Therapeutics, Inc. (the “Company”) issued a press release announcing,
among other things, certain financial and operational information for its fiscal year ended December 31, 2023 and provided a business
update. The full text of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
Item
7.01 Regulation FD Disclosure.
The
information included in Item 2.02 above is incorporated herein by reference. A copy of the press release is furnished as Exhibit
99.1 to this Current Report on Form 8-K and is incorporated herein by reference.
This
information is furnished pursuant to Item 7.01 of Form 8-K and shall not be deemed to be “filed” for the purposes of Section
18 of the Securities Exchange Act of 1934 or otherwise subject to the liabilities of that Section, unless we specifically incorporate
it by reference in a document filed under the Securities Act of 1933 or the Securities Exchange Act of 1934. By furnishing this information
on this Current Report on Form 8-K, we make no admission as to the materiality of any information in this report that is required to be
disclosed solely by reason of Regulation FD.
Item 9.01 Financial Statements and Exhibits.
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on our behalf by the
undersigned hereunto duly authorized.
|
Allarity Therapeutics, Inc. |
|
|
|
Date: March 8, 2024 |
By: |
/s/ Thomas Jensen |
|
|
Thomas Jensen |
|
|
Chief Executive Officer |
2
Exhibit
99.1
Allarity
Therapeutics Reports Full Year 2023
Financial Results and Provides a Business Update
| | - Leadership
Changes Led by Appointment of Co-Founder Thomas Jensen as Interim CEO and Jeremy Graff, Ph.D.,
former Eli Lilly Executive, as Executive Advisor |
| | - Reduced
Net Loss from Operations by 50% and Reduced Net Loss by 26% |
| | - Announced Data in
December 2023 from Advanced Ovarian Cancer Phase 2 Stenoparib Study Showing Significant Clinical
Benefit |
Boston
(March 8, 2024) — Allarity Therapeutics, Inc. (“Company”) (NASDAQ: ALLR), a clinical-stage pharmaceutical company
dedicated to developing personalized cancer treatments, today reported financial results for the year ended December 31, 2023, and provided
a general business update.
The
Company’s Interim Chief Executive Officer, Thomas Jensen, stated, “2023 was a year of remarkable achievements for Allarity
Therapeutics as we made significant strides in advancing our DRP®-guided drug development. Our clinical research has shown strong
indications that we can address a significant unmet medical need in oncology. In particular, our lead asset, stenoparib, has demonstrated
exceptional promise in advanced ovarian cancer trials. As we continue through 2024, our focus remains on continuing to generate and report
on additional pivotal clinical trial data for stenoparib, which we expect will further strengthen interest in our work from a broad group
of stakeholders, including leading oncologists, potential partner companies, and the biotech investor community.”
2023
Highlights and Recent Developments
Stenoparib
(2X-121): An orally available, small molecule dual-targeted inhibitor of poly-ADP ribose polymerase (PARP1/2) and telomerase maintenance
enzymes (Tankyrase 1 and 2) in development for advanced ovarian cancer.
| ● | Early
data announced in December 2023 from the Phase 2 monotherapy study of stenoparib for advanced
ovarian cancer showed significant clinical benefit in evaluable patients following a protocol
change to twice-daily dosing earlier in the year. Using the DRP®-Stenoparib
companion diagnostic (CDx), which includes 414 mRNA biomarkers, patients were selected based
on a DRP score above 50%. Of 22 screened, 17 were DRP positive, with 11 treated, of which
five were evaluable before the data evaluation cut-off. One trial participant showed a complete
response in December 2023, and the other four evaluable patients had stable diseases, all
were previously treated with PARP inhibitors and chemotherapy. |
Allarity
Therapeutics, Inc. | 210 Broadway, #201 | Cambridge, MA | U.S.A. | NASDAQ: ALLR | www.allarity.com
Announced
leadership changes and strategic advisory engagement:
| ● | Appointment
of co-founder Thomas H. Jensen as Interim Chief Executive Officer in December 2023. With
nearly two decades at Allarity Therapeutics, Jensen brings extensive experience and a deep
understanding of the company’s DRP® to his new role. Mr. Jensen has
been instrumental in developing molecular biological techniques essential for the DRP platform
and played a key role in building investor relations and securing financing. |
| | |
| ● | Engaged
Jeremy R. Graff, Ph.D., as an Executive Advisor. Dr. Graff, with over 25 years of experience
in biotech and pharma, is a specialist in both developing clinical strategy and successful
execution of numerous clinical development programs of cancer therapeutics. His notable career
includes C-level positions and a significant tenure at Eli Lilly, where he led the translational
oncology group. |
Anticipated
Clinical Milestones in 2024
The
focus of the Company remains on generating and disclosing pivotal clinical data to demonstrate the clinical benefit of our DRP guided
therapies. Accordingly, we expect to announce interim data from the DRP®-guided Phase 2 clinical trial of stenoparib in advanced
ovarian cancer during the second quarter of 2024. We believe that this milestone is particularly significant as it will provide further
insights into stenoparib’s potential to meet the unmet needs in the treatment of advanced ovarian cancer.
Full
Year 2023 Operating Results
R&D
Expenses: Research and Development (R&D) expenses were $7.1 million for 2023, compared to $6.9 million for 2022.
G&A
Expenses: General and Administrative (G&A) expenses were $10.0 million for 2023, compared to $10.0 million for 2022.
Net
Loss from Operations: Net Loss from Operations was $17.1 million for 2023, compared to $34 million for 2022.
Net
Loss: Net loss was $11.9 million for 2023, compared to $16.1 million for 2022.
About
the Drug Response Predictor – DRP® Companion Diagnostic
Allarity
uses its drug-specific DRP® to select those patients who, by the expression signature of their cancer, are found to have a high likelihood
of benefiting from a specific drug. By screening patients before treatment, and only treating those patients with a sufficiently high,
drug-specific DRP score, the therapeutic benefit rate may be significantly increased. The DRP method builds on the comparison of sensitive
vs. resistant human cancer cell lines, including transcriptomic information from cell lines combined with clinical tumor biology filters
and prior clinical trial outcomes. DRP is based on messenger RNA expression profiles from patient biopsies. The DRP® platform has
proven its ability to provide a statistically significant prediction of the clinical outcome from drug treatment in cancer patients in
37 out of 47 clinical studies that were examined (both retrospective and prospective). The DRP platform, which can be used in all cancer
types and is patented for more than 70 anti-cancer drugs, has been extensively published in the peer-reviewed literature.
About
Allarity Therapeutics
Allarity
Therapeutics, Inc. (NASDAQ: ALLR) is a clinical-stage biopharmaceutical company dedicated to developing personalized cancer treatments.
The Company is focused on development of stenoparib, a novel PARP/Tankyrase inhibitor for advanced ovarian cancer patients, using its
DRP® companion diagnostic for patient selection in the ongoing phase 2 clinical trial, NCT03878849. Allarity is headquartered in
the U.S., with a research facility in Denmark, and is committed to addressing significant unmet medical needs in cancer treatment. For
more information, visit www.allarity.com.
Allarity
Therapeutics, Inc. | 24 School Street, 2nd Floor | Boston, MA | U.S.A. | NASDAQ: ALLR | www.allarity.com
Follow
Allarity on Social Media
LinkedIn:
https://www.linkedin.com/company/allaritytx/
X:
https://twitter.com/allaritytx
Forward-Looking
Statements
This
press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of
1995. Forward-looking statements provide the Company’s current expectations or forecasts of future events. The words “anticipates,”
“believe,” “continue,” “could,” “estimate,” “expect,” “intends,”
“may,” “might,” “plan,” “possible,” “potential,” “predicts,”
“project,” “should,” “would” and similar expressions may identify forward-looking statements, but
the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements include, but are not
limited to, statements related to release of the clinical trial data in 2024 and its impact on strengthening interest in our work, the
availability of interim/final data readout from the DRP guided Phase 2 clinical trial of stenoparib for advanced ovarian cancer, the
possibility of a financing in Q1 2024 and expected availability of capital to fund its anticipated clinical trials, any statements related
to ongoing clinical trials for stenoparib as a monotherapy or in combination with another therapeutic candidate for the treatment of
advanced ovarian cancer, or ongoing clinical trials (in Europe) for IXEMPRA® for the treatment of metastatic breast cancer, statements
relating to the effectiveness of the Company’s DRP® companion diagnostics platform in predicting whether a particular patient
is likely to respond to a specific drug and statements related to the Company’s ability to regain compliance with the Nasdaq Listing
Rule. Any forward-looking statements in this press release are based on management’s current expectations of future events and
are subject to multiple risks and uncertainties that could cause actual results to differ materially and adversely from those set forth
in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that the Company
is not able to raise sufficient capital to support its current and anticipated clinical trials, the risk that early results of a clinical
study do not necessarily predict final results and that one or more of the clinical outcomes may materially change following more comprehensive
reviews of the data, and as more patient data become available, the risk that results of a clinical study are subject to interpretation
and additional analyses may be needed and/or may contradict such results, the receipt of regulatory approval for stenoparib or any of
our other therapeutic candidates and companion diagnostics or, if approved, the successful commercialization of such products, the risk
of cessation or delay of any of the ongoing or planned clinical trials and/or our development of our product candidates, the risk that
the results of previously conducted studies will not be repeated or observed in ongoing or future studies involving our therapeutic candidates,
and the risk that the current COVID-19 pandemic will impact the Company’s current and future clinical trials and the timing of
the Company’s preclinical studies and other operations. For a discussion of other risks and uncertainties, and other important
factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the section
entitled “Risk Factors” in our Form S-1 registration statement filed on October 30, 2023, as amended and our Form 10-K annual
report on file with the Securities and Exchange Commission (the “SEC”), available at the SEC’s website at www.sec.gov,
and as well as discussions of potential risks, uncertainties and other important factors in the Company’s subsequent filings with
the SEC. All information in this press release is as of the date of the release, and the Company undertakes no duty to update this information
unless required by law.
Allarity
Therapeutics, Inc. | 24 School Street, 2nd Floor | Boston, MA | U.S.A. | NASDAQ: ALLR | www.allarity.com
ALLARITY
THERAPEUTICS, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
For the years ended December 31, 2023 and 2022
(U.S. dollars in thousands, except for share and per share data)
| |
2023 | | |
2022 | |
Operating
expenses: | |
| | | |
| | |
Research
and development | |
$ | 7,103 | | |
$ | 6,930 | |
Impairment
of intangible assets | |
| — | | |
| 17,571 | |
General
and administrative | |
| 10,026 | | |
| 9,962 | |
Total
operating expenses | |
| 17,129 | | |
| 34,463 | |
Loss
from operations | |
| (17,129 | ) | |
| (34,463 | ) |
Other
income (expenses) | |
| | | |
| | |
Income
from the sale of IP | |
| — | | |
| 1,780 | |
Interest
income | |
| 22 | | |
| 30 | |
Interest
expenses | |
| (498 | ) | |
| (223 | ) |
Loss
on investment | |
| — | | |
| (115 | ) |
Foreign
exchange gains (losses) | |
| 133 | | |
| (913 | ) |
Fair
value of inducement warrants | |
| (4,189 | ) | |
| — | |
Loss
on modification of warrants | |
| (591 | ) | |
| — | |
Change
in fair value adjustment of warrant derivative liabilities | |
| 10,434 | | |
| 17,125 | |
Penalty
on Series A Preferred stock liability | |
| — | | |
| (800 | ) |
Net
other income, net | |
| 5,311 | | |
| 16,884 | |
Net
loss before tax recovery (expense) | |
| (11,818 | ) | |
| (17,579 | ) |
Deferred
income tax (expense) benefit | |
| (83 | ) | |
| 1,521 | |
Net
loss | |
| (11,901 | ) | |
| (16,058 | ) |
Cash
payable on converted Series A Preferred Stock | |
| — | | |
| (3,421 | ) |
Deemed
dividends on Series A Preferred Stock | |
| (8,392 | ) | |
| — | |
Deemed
dividend of on Series C Preferred Stock | |
| (123 | ) | |
| (1,572 | ) |
Net
loss attributable to common stockholders | |
$ | (20,416 | ) | |
$ | (21,051 | ) |
| |
| | | |
| | |
Basic
and diluted net loss per common stock | |
$ | (10.26 | ) | |
$ | (3,093.42 | ) |
Weighted
average number of common stock outstanding, basic and diluted | |
| 1,990,748 | | |
| 6,805 | |
Other
comprehensive loss, net of tax: | |
| | | |
| | |
Net
loss | |
$ | (11,901 | ) | |
$ | (16,058 | ) |
Change
in cumulative translation adjustment | |
| 310 | | |
| (121 | ) |
Comprehensive
loss attributable to common stockholders | |
$ | (11,591 | ) | |
$ | (16,179 | ) |
| All
common share data has been retroactively adjusted to effect reverse stock splits in 2023. |
Allarity
Therapeutics, Inc. | 24 School Street, 2nd Floor | Boston, MA | U.S.A. | NASDAQ: ALLR | www.allarity.com
ALLARITY
THERAPEUTICS, INC.
CONSOLIDATED BALANCE SHEETS
As of December 31, 2023 and 2022
(U.S. dollars in thousands, except for share and per share data)
|
|
December 31, |
|
|
December 31, |
|
|
|
2023 |
|
|
2022 |
|
ASSETS |
|
|
|
|
|
|
Current
assets: |
|
|
|
|
|
|
Cash |
|
$ |
166 |
|
|
$ |
2,029 |
|
Other
current assets |
|
|
209 |
|
|
|
1,559 |
|
Prepaid
expenses |
|
|
781 |
|
|
|
591 |
|
Tax
credit receivable |
|
|
815 |
|
|
|
789 |
|
Total
current assets |
|
|
1,971 |
|
|
|
4,968 |
|
Non-current
assets: |
|
|
|
|
|
|
|
|
Property,
plant and equipment, net |
|
|
20 |
|
|
|
21 |
|
Operating
lease right of use assets |
|
|
— |
|
|
|
6 |
|
Intangible
assets |
|
|
9,871 |
|
|
|
9,549 |
|
Total
assets |
|
$ |
11,862 |
|
|
$ |
14,544 |
|
LIABILITIES
AND STOCKHOLDERS’ (DEFICIT) EQUITY |
|
|
|
|
|
|
|
|
Current
liabilities: |
|
|
|
|
|
|
|
|
Accounts
payable |
|
$ |
8,416 |
|
|
$ |
6,251 |
|
Accrued
liabilities |
|
|
1,309 |
|
|
|
1,904 |
|
Warrant
derivative liability |
|
|
3,083 |
|
|
|
374 |
|
Income
taxes payable |
|
|
59 |
|
|
|
41 |
|
Convertible
promissory note and accrued interest, net of debt discount |
|
|
1,300 |
|
|
|
— |
|
Secured
promissory notes |
|
|
— |
|
|
|
2,644 |
|
Operating
lease liabilities, current |
|
|
— |
|
|
|
8 |
|
Total
current liabilities |
|
|
14,167 |
|
|
|
11,222 |
|
Non-current
liabilities: |
|
|
|
|
|
|
|
|
Convertible
promissory note and accrued interest, net of debt discount |
|
|
— |
|
|
|
1,083 |
|
Deferred
tax |
|
|
446 |
|
|
|
349 |
|
Total
liabilities |
|
|
14,613 |
|
|
|
12,654 |
|
Redeemable
preferred stock (500,000 shares authorized) |
|
|
|
|
|
|
|
|
Series
A Preferred Stock $0.0001 par value (20,000 shares designated) shares issued and outstanding at December 31, 2023 and 2022, were
1,417 and 13,586, respectively (liquidation preference of $17.54 at December 31, 2023) |
|
|
— |
|
|
|
2,001 |
|
Series
B Preferred Stock $0.0001 par value (200,000 shares designated); shares issued at December 31, 2023 and 2022, were 0 and 190,786,
respectively (liquidation preference of $0 at December 31, 2023) |
|
|
— |
|
|
|
2 |
|
Series
C Convertible Preferred stock $0.0001 par value (50,000 and 0 shares designated at December 31, 2023 and 2022, respectively);
shares issued and outstanding at December 31, 2023 were 0 |
|
|
— |
|
|
|
— |
|
Total
redeemable preferred stock |
|
|
— |
|
|
|
2,003 |
|
Stockholders’
(deficit) equity |
|
|
|
|
|
|
|
|
Series
A Preferred stock $0.0001 par value (20,000 shares designated) shares issued and outstanding at December 31, 2023 and 2022, were
1,417 and 13,586, respectively (liquidation preference of $17.54 at December 31, 2023) |
|
|
1,742 |
|
|
|
— |
|
Common
Stock, $0.0001 par value (750,000,000 and 30,000,000 shares authorized, at December 31, 2023 and 2022, respectively); shares
issued and outstanding at December 31, 2023 and 2022, were 5,886,934 and 11,356, respectively |
|
|
— |
|
|
|
— |
|
Additional
paid-in capital |
|
|
90,369 |
|
|
|
83,158 |
|
Accumulated
other comprehensive loss |
|
|
(411 |
) |
|
|
(721 |
) |
Accumulated
deficit |
|
|
(94,451 |
) |
|
|
(82,550 |
) |
Total
stockholders’ deficit |
|
|
(2,751 |
) |
|
|
(113 |
) |
Total
liabilities, preferred stock and stockholders’ (deficit) equity |
|
$ |
11,862 |
|
|
$ |
14,544 |
|
| All
common share data has been retroactively adjusted to effect reverse stock splits in 2023. |
###
Allarity
Therapeutics, Inc. | 24 School Street, 2nd Floor | Boston, MA | U.S.A. | NASDAQ: ALLR | www.allarity.com
Company
Contact:
investorrelations@allarity.com
Media
Contact:
Thomas
Pedersen
Carrotize
PR & Communications
+45
6062 9390
tsp@carrotize.com
Allarity
Therapeutics, Inc. | 24 School Street, 2nd Floor | Boston, MA | U.S.A. | NASDAQ: ALLR | www.allarity.com
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