Allarity Therapeutics Regains Compliance with Nasdaq's Minimum Stockholders' Equity Requirement
20 Mayo 2024 - 7:00AM
Boston (May 20, 2024)—Allarity
Therapeutics, Inc. (“Allarity” or the “Company”) (NASDAQ: ALLR), a
Phase 2 clinical-stage pharmaceutical company dedicated to
developing personalized cancer treatments, today announced that it
has received formal written notice from The Nasdaq Stock Market,
LLC’s Office of General Counsel (“Nasdaq”) that the Company has
regained compliance with the minimum stockholders' equity
requirement as set forth in Nasdaq Listing Rule 5550(b)(1) (the
“Equity Rule”).
This confirmation follows the Company’s successful efforts to
cut operation costs and improve its balance sheet, including
raising new equity and reducing outstanding liabilities. As a
result, Allarity Therapeutics now meets the stockholders' equity
requirement of at least $2.5 million.
Thomas Jensen, CEO of Allarity Therapeutics, stated, “We are
very pleased to announce that Allarity has regained compliance with
Nasdaq's equity requirement. During our panel hearing with Nasdaq
in February this year, we presented a strategic plan to achieve
this goal, and I am satisfied to note that we have successfully
delivered on our commitments and received formal confirmation from
Nasdaq. This allows us to continue focusing on our mission to
advance our lead asset, stenoparib, toward regulatory approval with
the aim of bringing this promising therapy to patients in need of
new treatment options for advanced ovarian cancer.”
As part of the compliance confirmation, Allarity Therapeutics
will be subject to a mandatory panel monitor for one year.
As announced in an earlier press release, the Company intends to
provide a more comprehensive clinical update in the near future to
share more details on the progress made following the early
conclusion of its Company's Drug Response Predictor (DRP®) guided
Phase 2 trial of stenoparib in advanced, recurrent ovarian
cancer.
About the Drug Response Predictor –
DRP® Companion
DiagnosticAllarity uses its drug-specific DRP® to select
those patients who, by the gene 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 dozens of
clinical studies (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 TherapeuticsAllarity
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.
Follow Allarity on Social MediaLinkedIn:
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, the impact of recent financial and operational
achievements on future quarterly performance, potential future
financings, and the anticipated regulatory progress of stenoparib
following the early conclusion of our Phase 2 clinical trial. 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 risks associated
with maintaining compliance with Nasdaq's continued listing
requirements, obtaining regulatory approval for stenoparib, and
potential market fluctuations that could impact our financial
stability and the drug's market entry. 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 April 17,
2024, 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.
###
Company Contact:
investorrelations@allarity.com
Media
Contact: Thomas
Pedersen Carrotize
PR &
Communications +45
6062 9390 tsp@carrotize.com
- Allarity Therapeutics Press Release - Nasdaq Confirms Equity
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