Decision marks first approval of a new oral anticoagulant in the USA in 50 years
INGELHEIM, Germany, Wednesday, October 20th 2010 [ME NewsWire]:
(BUSINESS WIRE)-- The US Food and Drug Administration (FDA) has approved Pradaxa® (dabigatran etexilate),1 Boehringer Ingelheim’s novel, oral direct thrombin inhibitor2 for stroke risk reduction in patients with non-valvular atrial fibrillation (AF) marking the first approval of a new oral anticoagulant in the U.S. in more than 50 years. The approval makes Pradaxa® available to a broad spectrum of patients, with the 150 mg bid dose approved for all patients except for a small subset with severe renal impairment (creatinine clearance 15-30 mL/min) where the approved dose is 75 mg bid.
The approval is based on findings from RE-LY®, the largest AF trial completed to date and is set to provide a breakthrough for stroke prevention in AF. The results demonstrated that dabigatran etexilate 150 mg significantly reduced the risk of stroke and systemic embolism by 35 percent beyond the reduction achieved with warfarin, the longtime standard of care, in addition to reductions in life-threatening and intracranial bleeding.3 Besides providing superior efficacy compared to warfarin, dabigatran etexilate does not require monitoring or related dose adjustments, is not affected by food, and no dose adjustment is required for many common co-medications in AF patients.
Physicians and patients in the US will now be the first to have access to this novel agent for this indication, which has the potential to change the treatment paradigm in stroke prevention in AF.
The RE-LY® trial showed for dabigatran etexilate compared with warfarin:3
* Significant reduction in the risk of stroke and systemic embolism – including haemorrhagic strokes with the 150mg bid dose
* Significantly lower major bleeding events with the 110mg bid dose
* Significantly lower life threatening and intracranial bleeding with both doses
* Significant reduction in vascular mortality with the 150mg bid dose.
Dr. Stuart Connolly, co-principal investigator of RE-LY®, Director, Division of Cardiology at McMaster University and member of The Population Health Research Institute, Hamilton, Ontario said, “Warfarin has been the standard therapy for stroke prevention in AF for many years. However, it is a very difficult treatment to use because of its interaction with various drugs, food types and the need for continuous monitoring to ensure that the drug is at the right therapeutic level. Anticoagulant monitoring is particularly burdensome and it is often difficult to maintain therapeutic range with warfarin, which puts patients at a higher risk of stroke or major haemorrhage. The approval of dabigatran etexilate provides for the first time an effective, flexible and convenient treatment option in the U.S., which will be especially important for the large group of patients who currently do not take any treatment because they cannot tolerate or refuse to take warfarin, or are not adequately controlled under current treatment.”
Well-controlled vitamin K antagonist (VKA) therapy (warfarin), currently used for the prevention of stroke in atrial fibrillation, is highly effective in reducing the risk of stroke by approximately two-thirds,4 but is associated with an increased risk of bleeding as well as several limitations. Drug-drug and food interactions as well as the requirement for frequent monitoring result in only about 50% of eligible patients receiving VKA therapy5 with fewer than half of these controlled within the therapeutic INR range.6
Professor Andreas Barner, Chairman of the Board of Managing Directors and responsible for the Corporate Board Division Research & Development and Medicine, Boehringer Ingelheim said, “This first approval of Pradaxa® for Stroke Risk reduction in Atrial Fibrillation in the US marks a new era for stroke prevention in atrial fibrillation. This is an important event in the 125-year history of Boehringer Ingelheim and is a very good example for Boehringer Ingelheim’s approach to provide “value through innovation”, i.e. through innovations in an area with high medical demand. This new treatment will improve the lives of many patients and with preventing stroke, will avoid suffering for a significant proportion of them. We expect that dabigatran etexilate will in the coming months become available to patients with atrial fibrillation in more countries, internationally.”
AF is the most common heart rhythm condition, affecting around 1% of the total population, rising to 10% in people over the age of 80.7 People with AF are at increased risk of blood clots, which raises stroke risk by five times,8,9 with up to three million people worldwide suffering strokes related to AF each year,10-12 which tend to be especially severe and disabling, with half of people dying within one year.13
- ENDS -
Please click on the link below for ‘Notes to Editors’ and ‘References’:
http://www.boehringer-ingelheim.com/news/news_releases/press_releases/2010/20_october_2010_dabigatran.html
For media enquiries, please contact:
Boehringer Ingelheim GmbH
Dr. Reinhard Malin, Corporate Communications
www.boehringer-ingelheim.com
Phone +49 6132 77-90815
Fax +49 6132 77-6601
No comments:
Post a Comment