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BTG Receives U.S. FDA 510(k) Clearance for EKOS® Control Unit 4.0 - BTG plc, the global specialist healthcare company, today announced U.S. Food and Drug Administration 510(k) clearance has been granted to the EKOS® Control Unit 4.0 - BTGplc.com
BTG Receives U.S. FDA 510(k) Clearance for EKOS® Control Unit 4.0

 

NewswireToday - /newswire/ - London, United Kingdom, 2017/02/27 - BTG plc, the global specialist healthcare company, today announced U.S. Food and Drug Administration 510(k) clearance has been granted to the EKOS® Control Unit 4.0 - BTGplc.com. LSE: BTG

   
 
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The EKOS® system includes an ultrasonic device that uses acoustic pulses, powered by the new Control Unit 4.0, to quickly and safely dissolve blood clots and restore blood flow in patients with pulmonary embolism (PE), deep vein thrombosis (DVT), and peripheral arterial occlusions (PAO).

The EKOS® Control Unit 4.0 was specifically designed to support a new standard of PE treatment allowing physicians to use one control unit to treat both pulmonary arteries. The color touchscreen allows physicians to easily monitor and independently manage two EKOS® devices simultaneously, simplifying bilateral PE treatment. With new functionality and workflow-based intelligence, the EKOS® Control Unit 4.0 is designed to support a medical team’s ability to perform at a high level from cath lab to transport to intensive care unit.

“Currently the only device cleared for the treatment of pulmonary embolism, EKOS® has been in a leadership position in the PE treatment market since the beginning” said BTG Vice President and General Manager Matt Stupfel. “Now, BTG is further solidifying our leadership position with the EKOS® Control Unit 4.0. This new platform will allow for further device innovation to simplify treatment for clinicians and improve outcomes for patients.”

Blood clots are tightly bound together in a fibrous mesh called fibrin. Fibrin blocks the flow of thrombolytic drugs, requiring higher drug doses to effectively dissolve the clot. The EKOS® system uses acoustic pulses to unwind and thin fibrin to expose drug receptor sites, allowing the drug to reach deeper into the clot, accelerating absorption and helping to dissolve the clot faster and with less thrombolytic.1

About Pulmonary Embolism
Pulmonary Embolism (PE) is a condition where one or more clots break off or travel from existing venous clots in the legs or arms and travel in the circulation, getting trapped in the lung, where they block the ability for blood to get to some areas of the lungs and receive oxygen. This may lead to a strain on the heart’s ability to pump blood through the lungs which can then lead to heart failure and/or cardiovascular collapse. PEs can be immediately fatal, but if PE can be diagnosed and appropriate therapy started, the mortality can be reduced from approximately 30 percent to less than 10 percent.2

About the EKOS® Endovascular System
The EKOS® system uses ultrasonic waves in combination with clot-dissolving thrombolytic drugs to effectively dissolve clots and restore healthy heart function and blood flow.

In clinical studies EKOS® therapy has been shown to speed time to clot dissolution, increase clot removal and enhance clinical improvement compared to either standard catheter-directed drug therapy or thrombectomy.1,3 EKOS® therapy requires significantly shorter treatment times and less thrombolytic compared to standard catheter-directed drug therapy4,5,6, lowering the risk of bleeding and other complications.1,6,7

Reference materials as the remarks in the press release:
1. Lin, P., et al.,“Comparison of Percutaneous Ultrasound-Accelerated Thrombolysis versus Catheter-Directed Thrombolysis in Patients with Acute Massive Pulmonary Embolism.” Vascular, Vol. 17, Suppl. 3, 2009, S137 S147.
2. Banovac, R et al.,"Reporting standards for endovascular treatment of pulmonary embolism." Journal of Vascular and Interventional Radiology, 2010; 21: 44-53.
3. Schrijver, am., et al.,“Dutch Randomized Trial Comparing Standard Catheter-Directed Thrombolysis and Ultrasound-Accelerated Thrombolysis for Arterial Thromboembolic Infrainguinal Disease (DUET)." Journal of Endovascular Therapy 2015, Vol. 22(1):87-95.
4. Litzendorf, M E., et al.,“Ultrasound-accelerated thrombolysis is superior to catheter-directed thrombolysis for the treatment of acute limb ischemia.” Journal of Vascular Surgery, Jun 2011; 53(Suppl S), p106S-107S.
5. Lin, P., et al.,“Catheter-Directed Thrombectomy and Thrombolysis for Symptomatic Lower-Extremity Deep Vein Thrombosis: Review of Current Interventional Treatment Strategies.” Perspectives in Vascular Surgery and Endovascular Therapy, 2010, 22(3): 152 163.
6. Parikh, S., et al.,“Ultrasound-Accelerated Thrombolysis for the Treatment of Deep Vein Thrombosis: Initial Clinical Experience.” Journal of Vascular and Interventional Radiology, Vol. 19, Issue 4, April 2008, 521 528.
7. Kucher, N., et al.,“Randomized, Controlled Trial of Ultrasound-Assisted Catheter-Directed Thrombolysis for Acute Intermediate-Risk Pulmonary Embolism.” Circulation, Vol. 129, No. 4, 2014, 479 486.

About BTG
BTG (btgplc.com) is a global specialist healthcare company bringing to market innovative products in specialist areas of medicine to better serve doctors and their patients. We have a portfolio of Interventional Medicine products to advance the treatment of cancer, severe emphysema, severe blood clots and varicose veins, and Specialty Pharmaceuticals that help patients overexposed to certain medications or toxins. Inspired by patient and physician needs, BTG is investing to expand its portfolio to address some of today’s most complex healthcare challenges.

EKOS is a registered trademark of EKOS Corporation, a BTG International group company. BTG and the BTG roundel logo are registered trademarks of BTG International LTD

Contacts:
Chris Sampson, Corporate Communications Director
P: +44(0)20 7575 1595 / M: +44(0)77 7325 1178

Chris Gale, Vice President - Greentarget Communications
P: +1 646-695-2883 / M: +1 203-570-4681.

 
 
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Written by / Agency / Source: Biocompatibles UK Ltd / BTG Plc

 
 

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BTG Receives U.S. FDA 510(k) Clearance for EKOS® Control Unit 4.0

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Publisher Contact: Hayley Senior - BTGplc.com 
+44(0)20 7575 1582 / +44(0)78 1577 8536 (mobile) chris.sampson[.]btgplc.com
 
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IMPORTANT INFORMATION: Issuance, publication or distribution of this press release in certain jurisdictions could be subject to restrictions. The recipient of this press release is responsible for using this press release and the information herein in accordance with the applicable rules and regulations in the particular jurisdiction. This press release does not constitute an offer or an offering to acquire or subscribe for any Biocompatibles UK Ltd / BTG Plc securities in any jurisdiction including any other companies listed or named in this release.

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