BioSpace.com

Biotech and Pharmaceutical
News & Jobs
Search the Site
 
   
Biotechnology and Pharmaceutical Channel Medical Device and Diagnostics Channel Clinical Research Channel BioSpace Collaborative    Job Seekers:  Register | Login          Employers:  Register | Login  

NEWSLETTERS
Free Newsletters
Archive
My Subscriptions

NEWS
News by Subject
News by Disease
News by Date
PLoS
Search News
Post Your News
JoVE

CAREER NETWORK
Job Seeker Login
Most Recent Jobs
Browse Biotech Jobs
Search Jobs
Post Resume
Career Fairs
Career Resources
For Employers

HOTBEDS
Regional News
US & Canada
  Biotech Bay
  Biotech Beach
  Genetown
  Pharm Country
  BioCapital
  BioMidwest
  Bio NC
  BioForest
  Southern Pharm
  BioCanada East
  US Device
Europe
Asia

DIVERSITY

INVESTOR
Market Summary
News
IPOs

PROFILES
Company Profiles

START UPS
Companies
Events

INTELLIGENCE
Research Store

INDUSTRY EVENTS
Biotech Events
Post an Event
RESOURCES
Real Estate
Business Opportunities

 News | News By Subject | News by Disease News By Date | Search News
eNewsletter Signup
Miles
Km80.5

   

BIOTRONIK Announces Initiation of ProMRI® Clinical Trial


1/16/2013 10:16:31 AM

Lake Oswego, Oregon, January 16th, 2013 – BIOTRONIK, a leading manufacturer of high-quality implantable cardiac devices and a pioneer of wireless remote monitoring technologies, announced today that the U.S. Food and Drug Administration (FDA) has approved, with conditions, the ProMRI® clinical trial via an Investigational Device Exemption. BIOTRONIK is sponsoring the trial (NCT01761162) and has already initiated U.S. site recruitment.

The ProMRI® clinical trial is designed to recruit 245 subjects implanted with one of BIOTRONIK’s cardiac devices that include ProMRI® technology at 30 U.S. investigational centers.

The ProMRI® clinical trial will evaluate BIOTRONIK’s Entovis dual- and single-chamber pacemaker systems after exposure to magnetic resonance imaging (MRI). These systems, which include BIOTRONIK’s current pacing leads, are already approved in the U.S. The trial will test the safety and effectiveness of the Entovis pacing system in patients undergoing MRI scans under predetermined conditions. The ultimate goal of the trial is to determine whether patients with these devices can safely undergo MRI scans. This could, in turn, provide access to important scanning procedures that will meet the future medical needs of patients implanted with BIOTRONIK pacemakers.

ProMRI® investigator Leon Feldman, M.D., at Eisenhower Memorial Hospital in Rancho Mirage, California, points out that, “While Entovis is not the first pacemaker proven safe in the MRI environment, if the endpoints are met, it will be the first device that includes all the modern features and capabilities electrophysiologists expect to have available in pacemakers and leads.” Dr. Feldman implanted the first Entovis system in a U.S. patient on December 26 last year. Additional Entovis implants have already been performed by Dr. Timothy Shinn at St. Joseph Mercy Hospital, Ann Arbor, Michigan and by Dr. Seth Goldbarg at New York Hospital Queens, Flushing, New York and by Dr. Jagmeet Singh at Massachusetts General Hospital, Boston, Massachusetts.

Entovis devices are renowned for their ability to provide the most advanced physiological therapy available via BIOTRONIK’s proprietary Closed Loop Stimulation (CLS) and BIOTRONIK Home Monitoring® technologies. BIOTRONIK’s active-fixation pacing leads have a flexible distal end, fractal coating, and steroid elution to provide excellent handling and stable fixation, as well as optimal electrical performance.

Several million patients currently are implanted with pacemaker systems worldwide. Previously published studies1,2 have projected that a sizeable proportion of these patients will develop a clinical need for an MRI scan during their lifetime. However, the strong forces applied during MRI have the potential to affect the pacemaker system negatively and, consequently, the patient’s safety. Therefore, these diagnostic scans currently are not recommended in patients with a pacemaker. Because MRI scanning often provides improved diagnostic capabilities for certain diseases or conditions that cannot be adequately examined by other imaging modalities, such as X-ray, computerized tomography (CT), or ultrasound, MRI compatible pacemaker systems are essential to comprehensive medical care.

"We are excited about demonstrating the safety of our pacemakers in the MRI environment," said Kevin Mitchell, Vice President of Clinical Studies for BIOTRONIK. "Estimates indicate that as many as 75 percent of patients implanted with pacemakers may require an MRI scan, and we look forward to ensuring that these patients have access to the procedure with the most technologically advanced pacemaker available"

The ProMRI® clinical trial is the first of several studies planned by BIOTRONIK to obtain safety and effectiveness data for its complete portfolio of cardiac rhythm devices with MRI conditional labeling, which the company intends to submit to review for approval by the FDA.'

References

1 Morgan Stanley, ICD market, 1996–2009.

2 Roguin et al., Europace 2008, 10, 336-346.

About BIOTRONIK SE & Co. KG

As one of the world’s leading manufacturers of cardiovascular medical devices, BIOTRONIK is headquartered in Berlin, Germany, and represented in over 100 countries by its global workforce of more than 5600 employees. Several million heart patients around the world have received BIOTRONIK implants, designed to save and improve the quality of their lives. Since its development of the first German pacemaker in 1963, BIOTRONIK has launched several innovations into the market—including remote monitoring with BIOTRONIK Home Monitoring® in 2000 and the world’s first implantable cardioverter-defibrillators and implantable heart failure therapy devices with ProMRI® technology, approved for MR scanning, in 2012. In 2013, BIOTRONIK will be celebrating its fiftieth anniversary.

For more information: www.biotronik.com

Contact U.S.

Rex Richmond

Vice President, Marketing & Communications

BIOTRONIK, Inc.

6024 Jean Road

Lake Oswego, OR 97035

(800) 547-0394, Ext. 8222

(503) 451-8222

Email: rex.richmond@biotronik.com

Contact Global:

Manuela Schildwächter

Global Communications Manager

BIOTRONIK SE & Co. KG

Woermannkehre 1

12359 Berlin

Tel. +49 (0) 30 68905 1466

Email: manuela.schildwaechter@biotronik.com



Read at BioSpace.com

   

ADD TO DEL.ICIO.US    ADD TO DIGG    ADD TO FURL    ADD TO STUMBLEUPON    ADD TO TECHNORATI FAVORITES