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Boehringer Ingelheim: New sub-analyses to be presented at ESC Congress 2018 further support positive safety profile of Pradaxa® (dabigatran etexilate)

August 20, 2018

INGELHEIM, Germany--(BUSINESS WIRE)--Aug 20, 2018--Boehringer Ingelheim today announced that it will present nine sub-analyses from the RE-DUAL PCI TM trial and GLORIA TM -AF Registry Program at the upcoming ESC Congress 2018, organised by the European Society of Cardiology, taking place in Munich, Germany on the 25-29 August 2018. The primary data from these studies have contributed to a positive label update for dabigatran etexilate (Pradaxa ® ) in the European Union (EU).

The primary RE-DUAL PCI TM trial investigated anticoagulation in patients with non-valvular atrial fibrillation (AF) following percutaneous coronary intervention (PCI) and stent placement. Data showed significantly lower rates of major or clinically relevant non-major bleeding events for dual therapy with dabigatran etexilate when compared to triple therapy with warfarin without compromise on efficacy. 1,2

GLORIA TM -AF is a large, prospective, observational study program run in over 40 countries worldwide. The primary analysis of nearly 5000 AF patients treated with dabigatran etexilate showed that the rates of stroke, major bleeding and life-threatening bleeding were low, confirming the sustained safety and effectiveness of dabigatran etexilate over two years of follow-up in clinical practice. 3 These data are consistent with the long-term safety profile observed in other real-world evidence studies, as well as in randomised clinical trials. 3

Both studies have helped to further confirm the safety profile of dabigatran etexilate in high risk patient populations, as well as in a real-world setting. In recognition of this, the European Medicines Agency (EMA) has recently authorised the inclusion of data from both studies within the SmPC for dabigatran etexilate in the EU. 4

“Insights from the RE-DUAL PCI TM and GLORIA TM -AF study data have helped to further inform the positive safety profile of dabigatran etexilate for the treatment of AF patients”, said Waheed Jamal, MD, Corporate Vice President & Head of Cardiometabolic Medicine at Boehringer Ingelheim. “We are pleased to see that the value these studies bring is also acknowledged by the EMA and the medical community. This is reflected by the updates to the EU SmPC and the number of abstracts accepted for presentation at ESC Congress 2018.”

Details of the data presented at ESC Congress 2018 are as follows:

More information on the Boehringer Ingelheim data due to be presented or published at the ESC Congress 2018 can be found here.

Intended audiences: This press release is issued from our Corporate Headquarters in Ingelheim, Germany and is intended to provide information about our global business. It is directed to the international audience outside Germany. Please be aware that information relating to the approval status and labels of approved products may vary from country to country, and a country-specific press release on this topic may have been issued in the countries where we do business.

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CONTACT: Boehringer Ingelheim

Corporate Communications

Media + PR

Meike Bausinger

Phone: +49 6132 77 182085

Mobile: +49 151 44061760

Fax: +49 6132 77 6601

Email:press@boehringer-ingelheim.com

KEYWORD: EUROPE GERMANY

INDUSTRY KEYWORD: HEALTH CLINICAL TRIALS PHARMACEUTICAL COMMUNICATIONS RESEARCH OTHER COMMUNICATIONS SCIENCE

SOURCE: Boehringer Ingelheim

Copyright Business Wire 2018.

PUB: 08/20/2018 03:00 AM/DISC: 08/20/2018 03:01 AM

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