BioCardia Announces Commercial Availability of Morph® DNA™ Steerable Introducer Product Family
17 Décembre 2024 - 1:00PM
BioCardia, Inc. [Nasdaq: BCDA], a global leader in cellular
and cell-derived therapeutics for the treatment of cardiovascular
and pulmonary diseases, announced today the commercial availability
of its Morph DNA steerable introducer product family, currently
utilized in the Company’s ongoing cell-therapy clinical trials.
“Our team is exploring an initial sales pipeline organically,
without expending the operating costs associated with engaging a
direct sales force or third-party medical device commercial
partners.” said BioCardia CEO, Peter Altman, PhD. “We look forward
to demonstrating the value of the Morph DNA product family to
physicians for procedures throughout the vascular system.”
Dr. Altman added, “BioCardia remains focused on our CardiAMP
Heart Failure I and II clinical trials, studying our
investigational FDA designated breakthrough cell therapy product
candidate to treat ischemic heart failure. We anticipate final
results in the CardiAMP Heart Failure I Trial and five actively
enrolling world class centers in the CardiAMP Heart Failure II
Trial by the end of the first quarter of 2025.”
About Morph DNA Steerable Introducers
Developed initially to provide enhanced control for
biotherapeutic delivery procedures within the heart, the Morph DNA
steerable introducer family has bidirectional steering, a
proprietary layup for torque response, ergonomic actuation, an
adjustable brake for fine control, and a swiveling side port in its
hemostasis valve to solve tangling issues and enhance
procedures.
Morph DNA designs contain tensioning elements in the catheter
that rotate around the catheter shaft, allowing consistent catheter
performance in any direction. The DNA name reflects this design, as
these tensioning elements resemble the double helix in a strand of
DNA. This design is intended to enable smooth navigation and
prevent “whip,” when the build-up of mechanical forces in the
device causes a catheter to suddenly jump from one orientation to
another.
A product brochure detailing available model numbers and sizes
is available on the Company’s website at brochure link.
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 advantages of the Morph DNA
design and expectations for data availability and enrollment in the
Company’s clinical trials. 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, 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
BioCardia (NASDAQ:BCDA)
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