Hancock Jaffe Announces Objectives for Upcoming CoreoGraft Study
28 Januar 2019 - 2:00PM
Hancock Jaffe Laboratories, Inc. (Nasdaq: HJLI, HJLIW), a Company
specializing in medical devices that restore cardiac and vascular
health, today announced its objectives for its upcoming CoreoGraft®
study at the Texas Heart Institute. The study will begin the week
of January 28.
The CoreoGraft animal study will focus on short
term graft patency and graft viability. Five CoreoGrafts will be
surgically implanted over a three-week period and continuously
monitored for thirty days for flow rates and patency using
transonic probes. The implantable probe will verify flows and
patency of the grafts. Following the monitoring part of the
trial, the CoreoGrafts will undergo pathology examinations to look
for evidence of cellular abnormalities that might lead to failure
or impact graft performance.
HJLI expects to provide an update after the
first implantation. The performance results of the study and the
pathology are expected to be released in April of 2019. Provided
that the study is successful, Hancock Jaffe would then seek a
Pre-FDA meeting to discuss the additional pre-clinical testing that
will be necessary for in-human trials.
Robert Berman, Hancock Jaffe’s Chief Executive
Officer stated, “Short term and long term saphenous vein graft
failures continue to be a major problem for patients undergoing
coronary bypass surgeries, and are a source of frustration for
cardiac surgeons and interventional cardiologists. The CoreoGraft
has the potential to set a new standard of care for the hundreds of
thousands of patients that undergo bypass surgery each year.”
HJLI’s CoreoGraft is a potential alternative to
using saphenous vein grafts (“SVGs”) to revascularize the heart
during coronary artery bypass graft (“CABG”) surgeries. The current
standard of care for most CABG surgeries is to harvest the SVG from
the leg of the patient, and to use pieces of the SVG as grafts to
revascularize the heart. In addition to the vein harvest procedure
being invasive, painful, and subject to its own complications for
the patient, SVGs are known to have high short term and long term
failure rates when used as grafts around the heart. Up to 40% of
SVGs fail within one year of CABG surgeries, with a significant
percentage failing within the first 30 days. Eight to ten years
after surgery, SVG failure rates are known to be in excess of 50%.
The risk of death from cardiac events increases significantly
following SVG failure.
Hancock Jaffe believes that its CoreoGraft will
avoid the two main causes of SVG failure: size mismatch (fluid
dynamics); and a thickening of the interior of the SVG graft that
begins immediately following the harvest procedure (known as the
“endothelial-to-mesenchymal transition” or “EndoMT”). Size
mismatch occurs because the diameter of SVGs is often significantly
larger than the diameter of the coronary arteries, causing flow
disturbances leading to graft thrombosis or development of intimal
hyperplasia resulting in graft failure. The diameter of HJLI’s
CoreoGrafts closely match the diameter of the coronary arteries,
eliminating the size mismatch which leads to clotting.
Scientists have discovered that the thickening
of the interior of SVG’s which leads to graft failure is caused by
a layer of endothelial cells on the inner surface of the SVG. When
the endothelial cells are disturbed as part of the SVG harvest
procedure, a chain reaction begins which causes the cells to
thicken and the inside of the graft to narrow, resulting in blood
clots and graft failure. Because the tissue used to make the
CoreoGrafts is completely different than SVG tissue, the CoreoGraft
may not suffer from the EndoMT that plagues SVGs.
Hancock Jaffe has two important studies starting
this quarter. In addition to the CoreoGraft study, HJLI will begin
first-in-human testing of its VenoValve®, a potential cure for
severe cases of chronic venous insufficiency, a debilitating
condition caused by venous reflux in the lower extremities and
which afflicts 4.5 million people in the U.S.
About Hancock Jaffe Laboratories, Inc.
HJLI specializes in developing and manufacturing
bioprosthetic medical devices to establish improved standards of
care for treating cardiac and vascular diseases. HJLI currently has
three product candidates: the porcine tissue based VenoValve®,
which is intended to be surgically implanted in the deep venous
system of the leg to treat Chronic Venue Insufficiency; the
CoreoGraft®, a bovine tissue based off the shelf conduit intended
to be used for coronary artery bypass surgery, and a porcine tissue
based heart valve, which based upon its relatively small size and
increased output, may be an ideal candidate for pediatric
aortic/mitral valve replacement.
Cautionary Note on Forward-Looking
Statements
This press release and any statements of
stockholders, directors, employees, representatives and partners of
Hancock Jaffe Laboratories, Inc. (the “Company”) related thereto
contain, or may contain, among other things, certain
"forward-looking statements" within the meaning of the Private
Securities Litigation Reform Act of 1995. Such
forward-looking statements involve significant risks and
uncertainties. Such statements may include, without
limitation, statements identified by words such as "projects,"
"may," "will," "could," "would," "should," "believes," "expects,"
"anticipates," "estimates," "intends," "plans," "potential" or
similar expressions. These statements are based upon the
current beliefs and expectations of the Company’s management and
are subject to significant risks and uncertainties, including those
detailed in the Company’s filings with the Securities and Exchange
Commission. Actual results (including, without limitation,
the performance of the new board members described herein) may
differ significantly from those set forth or implied in the
forward-looking statements. These forward-looking statements
involve certain risks and uncertainties that are subject to change
based on various factors (many of which are beyond the Company’s
control). The Company undertakes no obligation to publicly
update any forward-looking statements, whether as a result of new
information, future presentations or otherwise, except as required
by applicable law.
HJLI Press Contacts:
Amy CarmerTel: 949-261-2900Email: ACarmer@HancockJaffe.com
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