BioCardia Regains Full Compliance with Nasdaq Listing Requirements
18 September 2024 - 10:30PM
BioCardia, Inc. [Nasdaq: BCDA], a global leader in cellular and
cell-derived therapeutics for the treatment of cardiovascular and
pulmonary diseases, announced today that the Company has regained
full compliance with the Nasdaq Capital Market’s Listing
Requirements as required by the Hearing Panel’s (the “Panel”)
decision on May 13, 2024.
On September 17, 2024, BioCardia received notice
from Nasdaq confirming that the Company has demonstrated compliance
with Listing Rule 5550(b)(1) (the “Equity Rule”) of The Nasdaq
Stock Market. Accordingly, the Panel has determined to continue the
listing of the Company’s securities on the Nasdaq Stock Market and
is closing this matter.
This confirmation follows the Company’s
successful efforts to improve its balance sheet, including raising
new capital to continue development of its therapeutic candidates
and advance its approved products.
“It has been a busy past few weeks, with the FDA
approving the CardiAMP® Cell Therapy Heart Failure II protocol
amendment to use our proprietary Cell Population Analysis screening
to define each patient’s treatment plan, the University of
Wisconsin treating our last roll-in patient in the CardiAMP Cell
Therapy Chronic Myocardial Ischemia Trial, Helix™ partner
CellProthera having a positive pre-IND meeting with the FDA for
their cell therapy in acute myocardial infarction, our securing FDA
market clearance for our Morph® DNA™ product family, and our
closing a $7.2M financing to support our efforts ahead,” said Peter
Altman, PhD, BioCardia’s President and CEO. “We are delivering on
our mission to develop and enhance therapies to treat
cardiovascular and pulmonary disease, with our near-term focus on
finalizing CardiAMP HF I trial data for Japan PMDA and FDA,
randomizing first patients in the confirmatory pivotal CardiAMP HF
II trial, supporting Helix biotherapeutic delivery partners, and
manufacturing Morph DNA products for commercial use.”
About BioCardia:
BioCardia, Inc., headquartered in Sunnyvale,
California, is a global leader in cellular and cell-derived
therapeutics for the treatment of cardiovascular and pulmonary
disease. CardiAMP® autologous and CardiALLO™ allogeneic cell
therapies are the Company’s biotherapeutic platforms with three
clinical stage product candidates in development. These therapies
are enabled by its Helix™ biotherapeutic delivery and Morph®
vascular navigation product platforms.
Forward Looking Statements
This press release contains forward-looking
statements that are subject to many risks and uncertainties.
Forward-looking statements include, among other things, references
to the Company’s investigational product candidates, the potential
benefits of CardiAMP cell therapy for patients, enrollment in our
clinical trials, future regulatory submissions and approvals,
whether Helix partner CellProthera will advance their therapeutic
development with BioCardia, and the potential market for the
Company’s approved products. These forward-looking statements
are made as of the date of this press release, and BioCardia
assumes no obligation to update the forward-looking statements.
We may use terms such as “believes,”
“estimates,” “anticipates,” “expects,” “plans,” “intends,” “may,”
“could,” “might,” “will,” “should,” “approximately” or other words
that convey the uncertainty of future events or outcomes to
identify these forward-looking statements. Although we believe that
we have a reasonable basis for each forward-looking statement
contained herein, we caution you that forward-looking statements
are not guarantees of future performance and that our actual
results may differ materially from the forward-looking statements
contained in this press release as a result of one or more risk
factors. As a result of these factors, we cannot assure you that
the forward-looking statements in this press release will prove to
be accurate. Additional factors that could materially affect actual
results can be found in BioCardia’s Form 10-K filed with the
Securities and Exchange Commission on March 27, 2024, under the
caption titled “Risk Factors” and in its subsequently filed
Quarterly Reports on Form 10-Q. BioCardia expressly disclaims any
intent or obligation to update these forward-looking statements,
except as required by law.
Media Contact:
Miranda Peto, Marketing / Investor Relations
Email: mpeto@BioCardia.com
Phone: 650-226-0120
Investor Contact:
David McClung, Chief Financial Officer
Email: investors@BioCardia.com
Phone: 650-226-0120
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