Lombard Medical Announces Strategic Collaboration for its Refix™ Endostapler

London, UK, 14 December 2006 

 

Lombard Medical Technologies PLC (“Lombard Medical”) today announces a strategic collaboration with the leading US medical technology company, Medtronic Inc. (“Medtronic”), for Lombard Medical’s Refix™ Endostapler (“Refix™”).  Endostaplers are used to provide increased fixation of stent grafts which treat abdominal and thoracic aortic aneurysms, a balloon-like weakness in the artery wall. 


This strategic collaboration includes a distribution agreement whereby Medtronic has obtained the right to market Refix™ and will purchase Refix™ from Lombard Medical at an agreed transfer price.  Medtronic intends to market Refix™ under the trade name Securant.  Lombard Medical expects to complete the first clinical cases, following which Medtronic will initiate a controlled launch of the product.


The collaboration also includes a license agreement that allows Medtronic to use Lombard Medical’s Refix™ technology to develop “next generation” products in the field of cardiovascular disease.  Medtronic’s rights under this license agreement will commence provided that Medtronic elects to pay Lombard Medical a US$3 million licence fee following Refix’s™ approval by the FDA.  Royalties up to a maximum of US$5 million will also be payable by Medtronic to Lombard Medical on sales under the license agreement.  In addition, Medtronic will make available to Lombard Medical a loan facility of US$3 million.


Lombard Medical has retained co-distribution rights relating to the use of Refix™ with its own thoracic stent graft and has also retained exclusive rights in the large potential market for the endovascular fixation of percutaneous heart valves as well as potential applications in urinary and gastrointestinal surgery.  In addition, Lombard Medical has secured a licence to Medtronic’s Jervis/Raychem patent family in the endostapler field.  These patents relate to the use of nitinol in medical devices.


Lombard Medical’s Refix™ Endostapler is a device for the percutaneous delivery of tiny fasteners (staples), which are pushed through both the wall of the stent graft as well as the wall of the aorta, to keep the stent graft firmly in place.  Endovascular stent grafts provide vascular surgeons and interventional radiologists with a minimally invasive way to treat aneurysms. The stent graft re-routes the flow of blood into the aneurysm, thus avoiding the potential rupture of the balloon-like weakness, which could otherwise have fatal results.


Alistair Taylor, Executive Chairman of Lombard Medical, said:
“We are very pleased to enter into this strategic collaboration with Medtronic in the field of endovascular stapling. Medtronic is a world leader in the commercialisation of stent grafts for the treatment of aortic aneurysms and we look forward to the growth of Refix™ sales through Medtronic’s worldwide distribution channels. We also look forward to working with Medtronic to develop fixation devices for the next generation of aneurysm stent grafts.”

 

Enquiries:

 

Lombard Medical Technologies PLC Tel: 01235 750 800

Alistair Taylor, Executive Chairman
Brian Howlett, Chief Executive Officer
Tim Hall, Finance Director

 

Financial Dynamics Tel: 020 7831 3113
David Yates / John Gilbert

Notes to editors

 

About Lombard Medical
Lombard Medical Technologies PLC is a medical devices group developing stent grafts and other medical products for use in the treatment of vascular disease.  The Company’s lead product, Aorfix™, is a stent graft for the treatment of aortic aneurysms, a balloon-like enlargement of the aorta which, if untreated, may rupture and cause death.  Abdominal and thoracic aortic aneurysms are the 13th largest cause of death in the US and the market is estimated to be worth approximately US$2 billion by 2010.  Aorfix™ is currently being commercialised in the EU, with US clinical trials having commenced during 2006.   The Company’s Polymer Coatings Division primarily develops polymer coatings for use in drug eluting stents and has a number of research collaborations developing novel products for this $6bn market.


Lombard Medical has recently successfully completed its initial public offering on AIM and was admitted to listing in December 2005, raising £23.9 million, net of expenses.  The Company, based in Oxfordshire, Yorkshire and Boston, USA, employs over 90 people.


Further background on the Company can be found at www.lombardmedical.com.

 



Date   

Title

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
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1/29/2010 10:40:00 AM
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John B. Rush appointed CEO at Lombard Medical
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2009 Oxford and South East Bioscience Award for Best Medtech Fundraising
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FDA acceptance of the first of six modules of PMA filing for Aorfix™
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Interim results for the six months ended 30 June 2009
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Report and Accounts
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AGM May 2009 Results
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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
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Placing and Subscription to raise £6.1 million
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EndoRefix™ Trial Suspended
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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
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Update
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£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
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Lombard Medical Placing announcement
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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
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Yorkshire Forward Grant for Development of Urinary Catheters
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Successful Clinical Cases
1/30/2007 12:00:00 PM
Recommencement of European Clinical Procedures For Second Generation Stent Graft
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Board Change
12/14/2006 10:18:00 AM
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Lombard Medical Technologies PLC Total Voting Rights and Share Capital
12/11/2006 4:47:00 PM
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11/10/2006 12:04:00 PM
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11/8/2006 2:23:00 PM
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Positive 24 month Clinical Data for Aorfix™ Stent Graft
8/25/2006 10:42:00 AM
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8/25/2006 10:15:00 AM
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Annual General Meeting
4/13/2006 3:30:00 PM
Positive 12 month Clinical Data for Aorfix™ Stent Graft
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Research Agreement with Amgen and University of Sheffield
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Company Completes Successful Year
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CE Mark and conditional IDE approval received for second-generation EndoRefix™
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Lombard Medical receives full IDE approval for its US clinical trial of its Aorfix™ stent graft
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Application for admission of ordinary shares
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1/17/2006 3:43:00 PM
Application for admission of ordinary shares
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