INGELHEIM, Germany, Friday, October 23rd 2009
 
 
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CHMP Issues Positive Opinion for MICARDIS (telmisartan) as the First Treatment in Its Class to Reduce the Risk of Cardiovascular (CV) Morbidity in High CV Risk Patients

 

INGELHEIM, Germany, Friday, October 23rd 2009 [ME NewsWire]:

  • MICARDIS (telmisartan) is set to be the ONLY treatment in its class with this indication, demonstrating proven cardiovascular (CV) protection in patients at high CV risk
  • The ONTARGET Trial results reviewed by the CHMP showed that MICARDIS may prevent one in five serious CV events1
  • Patients at-risk of heart attack and stroke will benefit from this new indication if approved.

(BUSINESS WIRE)-- Boehringer Ingelheim announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Evaluation Agency (EMEA) has issued a positive opinion for the approval of MICARDIS (telmisartan) for the reduction of cardiovascular morbidity in patients with:

I. manifest atherothrombotic cardiovascular disease (history of coronary heart disease, stroke, or peripheral arterial disease) or

II. type 2 diabetes mellitus with documented target organ damage.

The CHMP opinion follows a review of clinical trial results including The ONTARGET Trial involving 25,620 patients and confirmed MICARDIS as the only treatment option in its class with proven cardiovascular protective effects in patients with high CV risk.1 The results also demonstrated that MICARDIS is

better tolerated than the previous gold standard ramipril and is associated with higher treatment adherence.1-2

Professor Klaus Dugi, Corporate Vice President Medical Affairs, Boehringer Ingelheim, commented, “We are delighted to receive this positive opinion from the CHMP. This is an important development that may help physicians ensure that patients receive appropriate treatment tailored to their individual needs. If approved, MICARDIS will offer a much needed alternative to ACE inhibitors.”

Earlier this week, the US Food and Drugs Administration (FDA) approved MICARDIS for the reduction of the risk of myocardial infarction (heart attack), stroke, or death from cardiovascular (CV) causes in patients 55 years of age or older at high risk of developing major CV events who are unable to take ACE inhibitors.

  • Cardiovascular disease (CVD) is responsible for nearly one in three deaths worldwide and is the number one cause of death3
  • CVD causes nearly half of all deaths in Europe (48%) and in the EU (42%).4 About half of all deaths from CVD are from coronary heart disease and nearly one-third are from stroke5
  • 15 million people each year suffer strokes and 5 million are left permanently disabled6

MICARDIS® is one of the most studied antihypertensives in clinical trials and is widely used with over five million patient years since its approval. Its safety profile is similar to that of placebo.

~ENDS~

To view notes to editors and references, click on the link below:

http://www.boehringer-ingelheim.com/corporate/news/press_releases/detail.asp?ID=7015
For media enquiries, please contact:
Boehringer Ingelheim GmbH
Dr.
Reinhard Malin,
Tel: + 49 - 6132 - 77 90815
Corporate Division Communications
Fax: + 49 - 6132 - 72 6601
E-mail: reinhard.malin@boehringer-ingelheim.com
 
 
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