Lombard Medical Technologies PLC First U.S. patients treated with Aorfix (4682M)
August 27 2013 - 2:01AM
UK Regulatory
TIDMLMT
RNS Number : 4682M
Lombard Medical Technologies PLC
27 August 2013
Lombard Medical Technologies PLC
("Lombard Medical" or "Company")
LOMBARD MEDICAL ANNOUNCES FIRST U.S. PATIENTS TREATED
WITH AORFIX FLEXIBLE AORTIC STENT GRAFT
Only Endovascular Stent Graft Approved in U.S. for Use in Most
Challenging
Abdominal Aortic Aneurysm Cases
London, UK and Irvine, CA, August 27 2013 - Lombard Medical
Technologies PLC (AIM: LMT), the specialist medical technology
company focused on innovative vascular products, today announces
that the first U.S. patients have been successfully treated with
Aorfix(TM), the Group's flexible stent graft for the endovascular
repair of abdominal aortic aneurysms (AAAs).
Aorfix was approved by the FDA for commercial sale in the U.S.
in February 2013. The approval included a label indication for the
treatment of patients with angulations at the neck of the aneurysm
from 0 to 90 degrees. Moreover, Aorfix is the only endovascular
stent graft with approved labeling for use in more challenging
cases with neck angulations greater than 60 degrees.
The first U.S. cases using Aorfix included patients with aortic
neck angles significantly greater than 60 degrees that would have
previously required more invasive open surgical AAA repair or "off
label" use of an alternative device not designed to treat patients
with this level of tortuosity in the aorta. The patients were
treated by Victor J. Weiss, M.D., a vascular surgeon at Meriter
Hospital in Madison, WI and Sachinder Hans, M.D. of Henry Ford
Hospital in Detroit, respectively. Kim Hodgson, M.D. of Southern
Illinois University School of Medicine, Division of Vascular
Surgery, Springfield, Illinois, also reported a further case where
the patient was successfully treated using Aorfix. All patients are
doing well following the procedures.
Simon Hubbert, Chief Executive Officer of Lombard Medical
said:
"We are delighted to see the first patients being treated with
Aorfix since the FDA granted approval earlier this year. Previously
these patients would have received more invasive open surgery
repair or would have been treated using a less flexible
endovascular device, unlicensed to treat high aortic neck angles.
Since receiving U.S. FDA approval, the Company has invested in the
right people and worked diligently to ensure we have the commercial
infrastructure and processes in place to become a significant
player in the AAA market in the United States."
Dr. Victor Weiss commented:
"The flexible design of Aorfix promises to make it possible to
treat the most challenging patients and provides a less invasive
treatment option to open surgery repair. Based on my initial
experience with Aorfix, I believe its ease of use and unique design
will provide us with an important new tool to ensure the
effectiveness of endovascular treatment of AAAs."
Dr. Sachinder Hans added:
"I was particularly impressed by how Aorfix conformed to a very
challenging anatomy. This patient had several health issues that
existed prior to the procedure, including poor renal function and
heavy calcium deposits, but we had a very successful outcome due to
our ability to address the AAA in a minimally invasive fashion.
Aorfix provides a new and important addition to the armamentarium
of physicians working with patients with AAAs."
-Ends-
For further information:
Lombard Medical Technologies PLC Tel: +44(0)1235 750 800
Simon Hubbert, Chief Executive Officer
Ian Ardill, Chief Financial Officer
Canaccord Genuity Limited Tel: +44(0)20 7523 8000
Lucy Tilley / Tim Redfern / Henry
Fitzgerald O'Connor / Dr Julian Feneley
FTI Consulting Tel: +44(0)20 7831 3113
Simon Conway / Susan Stuart / Victoria
Foster Mitchell
Allen & Caron Tel: +1 (949) 474 4300
Matt Clawson
About Abdominal Aortic Aneurysms
AAAs are a balloon-like enlargement of the aorta which, if left
untreated, may rupture and cause death. Approximately 4.5 million
people are living with AAAs in the developed world and each year
600,000 new cases are diagnosed. In the U.S. aortic aneurysm
disease is among the leading cause of death and it is estimated
that 1.7 million people over the age of 55 have an AAA. The market
for the repair of AAAs in the U.S. is valued at more than $600
million annually, and is forecast to grow to $1.6 billion worldwide
by 2015 according to independent market research.
About Lombard Medical
Lombard Medical Technologies PLC (AIM: LMT) is a medical device
company focused on device solutions for the $1.3 billion per annum
abdominal aortic aneurysm (AAA) repair market. The Company's lead
product, Aorfix, is an endovascular stent graft which has been
specifically designed to solve the problems that exist in treating
complex tortuous anatomy, which is often present in advanced AAA
disease. Aorfix is the only stent graft approved for AAA neck
angulations of up to 90 degrees and is currently being
commercialized worldwide. Aorfix is the first AAA stent graft not
of U.S. origin to gain FDA approval. The Company is headquartered
in Oxfordshire, England with U.S. operations in Irvine, CA.
Further background on the Company can be found at
www.lombardmedical.com.
This information is provided by RNS
The company news service from the London Stock Exchange
END
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