Study shows that Aorfix™ Reduces Iliac Limb Occlusion Rates from 7.5% to 0%

 

London, UK, 15 April 2010 – Lombard Medical Technologies PLC (AIM: LMT), announced today that Dr John Hardman has presented data this week at the 32nd International Charing Cross Symposium on the use of Aorfix™ in patients with tortuous iliac anatomy. The study was performed at the Royal United Hospital in Bath, UK.


The aim of the study was to evaluate the use of Lombard Medical’s Aorfix™ Stent Graft on the rate of iliac limb occlusion.  The study had two arms, a control group and a study group.  Aorfix™ was used in the study group only.


The control group included 93 patients, 12 of whom were considered to be severely angulated or required adjunctive stenting (12.9%).  7 patients in the control group developed iliac limb occlusions (7.5% occlusion rate), and 5 of these 7 patients required an additional intervention during the first two weeks post procedure. 


The study group included 168 patients, 25 of whom were considered to be severely angulated (14.8%).  Iliac limb occlusions were eliminated completely in this group (0% occlusion rate).  The Aorfix™ stent graft was utilized in 40 of the most severely angulated cases in the study group.
Dr Hardman concluded his presentation by stating that:


 “In our experience, having Aorfix™ available allows us to treat more patients with an endovascular approach.  Furthermore, we have seen a dramatic improvement in our iliac limb occlusion rates when utilizing the Aorfix™ stent graft.”

 

- Ends -


About Lombard Medical
Lombard Medical Technologies PLC (AIM: LMT), is a medical device company focused on device solutions for the $1 billion dollar abdominal aortic aneurysm (AAA) repair market. AAA’s 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 AAA’s in the developed world and each year 600,000 new cases are diagnosed. The market for endovascular stent grafts for this application is expected to grow to $1.6 billion by 2015.  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 currently being commercialised in the EU, with a pivotal clinical trial ongoing in the USA.  
The Company is headquartered in Oxfordshire, with operations in Ayrshire and Phoenix, USA.
Further background on the Company can be found at www.lombardmedical.com.

 

For further information:

Lombard Medical Technologies PLC 
John Rush, Chief Executive Officer
Tim Hall, Finance Director 

Tel: 01235 750 800

 

Evolution Securities Limited 
Barry Saint
Tel : 020 7071 4300

 

Financial Dynamics 
Jonathan Birt
Tel : 020 7831 3113


 



Date   

Title

8/23/2010 11:37:00 AM
Interim results for the six months ended 30 June 2010
8/9/2010 12:49:00 PM
FDA approves the third of six modules for Aorfix™ PMA filing
5/20/2010 2:12:00 PM
AGM RESULTS
5/20/2010 1:33:00 PM
AGM 2010 - Trading Update
5/4/2010 12:17:00 PM
Senior Medical Device Sales and Marketing Executive Joins Lombard Medical
4/20/2010 2:53:00 PM
Positive Aorfix™ Data Reported at Charing Cross Symposium
4/16/2010 1:39:00 PM
Preliminary Results for the Year ended 31 December 2009
4/15/2010 12:05:00 PM
Study shows that Aorfix™ Reduces Iliac Limb Occlusion Rates from 7.5% to 0%
3/24/2010 11:21:00 AM
Professor Don Ricci - Board Appointment
3/10/2010 1:25:00 PM
International Congress (XXIII) Endovascular Interventions
2/5/2010 3:19:00 PM
Share Option Grant
2/2/2010 5:27:00 PM
Total Voting Rights
2/1/2010 1:16:00 PM
Result of General Meeting
1/29/2010 10:40:00 AM
Result of offer to qualifying shareholders and qualifying employees
1/13/2010 4:25:00 PM
Issue of equity to raise £13 million
12/24/2009 11:22:00 AM
Change of Nominated Adviser and Broker
11/17/2009 10:59:00 AM
Disposal of Polymer Coatings Business to Bayer
10/12/2009 10:03:00 AM
John B. Rush appointed CEO at Lombard Medical
9/23/2009 12:55:00 PM
Further Positive Aorfix™ Data Reported at CIRSE and TCT
9/11/2009 2:04:00 PM
2009 Oxford and South East Bioscience Award for Best Medtech Fundraising
9/2/2009 10:51:00 AM
FDA acceptance of the first of six modules of PMA filing for Aorfix™
8/7/2009 1:06:00 PM
Interim results for the six months ended 30 June 2009
6/18/2009 1:24:00 PM
Report and Accounts
6/4/2009 1:08:00 PM
European Label Claim Extension for Aorfix™ to Treat Patients with High-angle-neck Aneurysms
5/20/2009 11:48:00 AM
AGM Trading Update
5/20/2009 11:45:00 AM
AGM May 2009 Results
4/6/2009 10:58:00 AM
Positive Aorfix™ Data in Challenging Anatomies Reported at Charing Cross Symposium
4/1/2009 10:58:00 AM
Preliminary Results for year ended 31 December 2008
3/12/2009 4:34:00 PM
Lombard Medical Regains Marketing Rights for EndoRefix™
2/27/2009 12:38:00 PM
NICE Guidelines for the Treatment of Abdominal Aortic Aneurysms
1/29/2009 2:19:00 PM
Share Option Grant
1/13/2009 2:56:00 PM
Employee Consultation regarding Redundancies
1/12/2009 1:16:00 PM
Fundraising Circular
1/9/2009 11:40:00 AM
Placing and Subscription to raise £6.1 million
12/10/2008 11:09:00 AM
EndoRefix™ Trial Suspended
11/26/2008 10:40:00 AM
Growing positive experience of Aorfix™ across the world - Approval received for Aorfix™ in Russia
11/24/2008 4:19:00 PM
US Trial and Further Cost Cutting Measures
10/17/2008 5:06:00 PM
Update
9/26/2008 10:46:00 AM
£1.6 million fundraising
9/22/2008 11:22:00 AM
European Arbiter II Trial Completes Recruitment
8/15/2008 6:14:00 PM
Interim Results for the six months ended June 2008
5/12/2008 12:10:00 PM
AGM Trading Update
4/30/2008 11:22:00 AM
US EndoRefix™ Pivotal Trial commences
4/16/2008 12:16:00 PM
FDA Acceptance for Aorfix™ as a Modular PMA and Successful Charing Cross Symposium
3/20/2008 11:27:00 AM
Preliminary Results for Year ended 31 December 2007
1/16/2008 11:29:00 AM
Lombard Directors' Share Purchase
1/14/2008 12:38:00 PM
Result of Lombard EGM and Company Strategy Update
1/8/2008 3:00:00 PM
NHS screening programme for treatment of AAA
12/20/2007 10:22:00 AM
Fundraising of £7.6 million
11/19/2007 11:15:00 AM
Aorfix™ successfully passes 21- patient case review by FDA
10/22/2007 12:31:00 PM
CE Mark and conditional IDE approval received for second-generation EndoRefix™
9/20/2007 11:34:00 AM
Lombard Medical Announces board changes
9/20/2007 11:23:00 AM
Lombard Medical Announces interim results 2007
7/30/2007 11:12:00 AM
Lombard Medical Receives Full FDA Approval of its Supplemental IDE to Pivotal US Clinical Trial
7/13/2007 10:19:00 AM
First US Case in a Patient with a High Angle Neck Aneurysm using Gen II Aorfix™
7/5/2007 3:27:00 PM
Lombard Medical enters into Collaboration with Smith & Nephew to Develop Bioresorbable Drug-eluting Coronary Stents
6/20/2007 1:42:00 PM
Lombard Medical Announces the Acquisition of Culzean Medical Devices Limited
6/15/2007 12:51:00 PM
Lombard Medical Placing announcement
6/15/2007 12:34:00 PM
Lombard Medical announces 2006 Results
5/31/2007 11:52:00 AM
Lombard Medical Receives Conditional FDA Approval of its Supplemental IDE to Pivotal US Clinical Trial
5/22/2007 12:23:00 PM
First Cases for Aorfix™ in Brazil
4/23/2007 6:35:00 PM
Lombard Medical Announces Filing of Supplemental IDE to Pivotal US Clinical Trial for Aorfix™ and Provides Progress Update
4/4/2007 1:24:00 PM
Lombard Medical receives FDA approval of its Supplemental IDE to use "Gen II" Aorfix™ in Pivotal US Clinical Trial
2/23/2007 11:06:00 AM
Trade Investment in Endoart SA
2/12/2007 12:27:00 PM
Yorkshire Forward Grant for Development of Urinary Catheters
2/5/2007 12:22:00 PM
Successful Clinical Cases
1/30/2007 12:00:00 PM
Recommencement of European Clinical Procedures For Second Generation Stent Graft
1/9/2007 1:52:00 PM
Board Change
12/14/2006 10:18:00 AM
Lombard Medical Announces Strategic Collaboration for its Refix™ Endostapler
12/11/2006 5:00:00 PM
Lombard Medical Technologies PLC Total Voting Rights and Share Capital
12/11/2006 4:47:00 PM
Temporary Suspension of European Clinical Procedures For Second Generation Stent Graft
11/10/2006 12:04:00 PM
Lombard Medical announces receipt of CE Mark for its Refix™ Endostapler
11/8/2006 2:23:00 PM
Lombard Medical receives conditional FDA approval of its supplemental IDE for Aorfix™
10/2/2006 12:59:00 PM
Lombard Technologies PLC announces a Collaboration for the Development of a Next Generation Regenerative Stent
9/11/2006 10:32:00 AM
Positive 24 month Clinical Data for Aorfix™ Stent Graft
8/25/2006 10:42:00 AM
Lombard Medical Technologies PLC Trading Update
8/25/2006 10:15:00 AM
Lombard Medical Technologies PLC retains distribution rights for Aorfix™, AAA and Thoracic Stent Grafts
8/3/2006 1:27:00 PM
Lombard Medical enters into collaboration with Axordia for stem cell derived drug eluting stents
5/10/2006 10:31:00 AM
Annual General Meeting
4/13/2006 3:30:00 PM
Positive 12 month Clinical Data for Aorfix™ Stent Graft
4/4/2006 5:07:00 PM
Research Agreement with Amgen and University of Sheffield
3/24/2006 4:44:00 PM
Company Completes Successful Year
2/24/2006 10:59:00 AM
CE Mark and conditional IDE approval received for second-generation EndoRefix™
2/17/2006 2:25:00 PM
Lombard Medical receives full IDE approval for its US clinical trial of its Aorfix™ stent graft
2/15/2006 9:22:00 PM
Application for admission of ordinary shares
2/10/2006 9:18:00 PM
Lombard Medical Announces that Abdominal Aortic Aneurysm Screening to Commence in the US
1/19/2006 2:41:00 PM
Lombard Medical reports new data demonstrating that its Aorfix™ stent graft reduces the risk of endoleaks in angulated necks
1/19/2006 2:16:00 PM
Directors share purchase
1/17/2006 3:43:00 PM
Application for admission of ordinary shares
12/13/2005 3:46:00 PM
Lombard Medical Technologies PLC commences trading on AIM
12/7/2005 9:08:00 PM
Lombard Medical Technologies PLC raises £26.2 million on successful completion of IPO