Berlin Heart Inc. Receives FDA Orphan Product Development Grant
Posted on: Wednesday, 17 June 2009, 12:32 CDT
The Berlin Heart EXCOR Pediatric VAD is a system for mechanical support
of the heart in end-stage heart failure patients. It has been specifically
designed for use in pediatric patients of all age groups ranging from
newborns to teenagers. The device received unconditional approval for
investigational use in pediatric patients in the US in
The goal of the Office of Orphan Products Development Grant Program is to encourage clinical development of products for use in rare diseases or conditions. At this time, only clinical studies qualify for consideration. All studies must be conducted under an Investigational New Drug (IND) application or an Investigational Device Exemption (IDE). The grant awarded to Berlin Heart provides three years of support.
The number of grant awards varies each year depending on the availability of funds. On-going studies are funded first with the remainder of funds going to new studies. In recent years, the Office of Orphan Products Development Grant Program has funded approximately twelve to fifteen new awards annually.
About EXCOR(R) Pediatric
The EXCOR Pediatric Ventricular Assist Device is a mechanical cardiac support system for critically ill pediatric patients suffering from severe heart failure. EXCOR Pediatric has been used in more than 500 pediatric patients worldwide ranging from newborns with 2.2 kg body weight to teenagers. EXCOR is currently under clinical investigation for pediatric patients in USA.
About Berlin Heart
Berlin Heart GmbH is the only company worldwide that develops, produces,
and distributes implantable and external ventricular assist devices (also
called mechanical heart support systems) for patients of every age and body
size. The company is market leader in
The company also manufactures the implantable left ventricular assist
device INCOR(R), which has been designed for long-term application in adult
patients. The longest the device has supported a patient so far is more than
five and a half years and ongoing. INCOR is not FDA approved, but widely used
in
SOURCE Berlin Heart GmbH
Source: PR Newswire
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