INGELHEIM, Germany - Monday, June 22nd 2015 [ME NewsWire]
First patient study data show that idarucizumab* immediately reverses dabigatran within minutes in patients requiring urgent procedures or with serious bleeding complications1,2
Interim analysis from RE-VERSE AD™, the first study investigating the effect of a specific reversal agent to a NOAC with patients in a real-world setting
Data are published in the New England Journal of Medicine and presented at the ISTH 2015 Congress1,2
(BUSINESS WIRE)-- Results from an interim analysis of the Phase III RE-VERSE AD™ patient study demonstrate that 5 g of idarucizumab* immediately reversed the anticoagulant effect of dabigatran (Pradaxa®) in patients requiring urgent anticoagulant reversal. No safety concerns relating to idarucizumab* were identified. The results have been simultaneously published in the New England Journal of Medicine (NEJM) and presented today at the International Society of Thrombosis and Haemostasis 2015 Congress in Toronto, Canada.1,2
“The interim analysis from RE-VERSE AD™ is important for healthcare professionals as it provides the first insights into the effect of a specific reversal agent to a non-vitamin K antagonist oral anticoagulant during real-world emergency situations,” said Dr. Charles Pollack, Professor of Emergency Medicine at the Perelman School of Medicine, University of Pennsylvania in Philadelphia, USA, and lead investigator of the patient study. “As observed in earlier research in volunteers, idarucizumab* reversed the anticoagulant effect of dabigatran in patients completely within minutes, even in those rare critical care situations studied in RE-VERSE AD™. These data demonstrate that use of idarucizumab* can help physicians focus on other vital aspects of emergency management beyond anticoagulant reversal in dabigatran-treated patients.”
RE-VERSE AD™ is designed to evaluate the types of patients and real-world situations healthcare professionals may see in emergency settings.1,3 The broad inclusion criteria ensure that even the most severely ill or injured patients (e.g. patients with sepsis or a severe intracranial haemorrhage), who require urgent reversal of dabigatran, may be enrolled in the study.1,3 Patients were categorised into two groups – (A) patients with uncontrolled or life-threatening bleeding complications, e.g. intracranial haemorrhage or severe trauma after a car accident (Group A, n= 51), or (B) patients requiring emergency surgery or an invasive procedure, e.g. surgery for an open fracture after a fall (Group B, n=39).1,3 The primary endpoint of the study is the degree of reversal of the anticoagulant effect of dabigatran achieved by 5 g idarucizumab* within 4 hours measured by diluted thrombin time (dTT) and ecarin clotting time (ECT).3
The interim analysis from RE-VERSE AD™ included data from 90 patients in emergency settings who were taking dabigatran and required reversal. Of the 81 patients that presented with elevated anticoagulation levels at baseline as measured with ECT, results showed:1
The study met its primary endpoint, achieving 100 per cent maximum reversal as median value across all patients
Reversal was evident immediately after administration of the first vial of idarucizumab* and was complete in all but 1 patient
After 4 and 12 hours, laboratory tests showed normal coagulation levels in almost 90 per cent of patients
Normal blood clotting (haemostasis) during surgery was reported in 92 per cent of the patients that required surgery or invasive procedures
There was no signal of a pro-coagulant effect following administration of idarucizumab*
Thrombotic events occurred in five patients, none of whom were receiving antithrombotic therapy at the time of the event
There were 18 deaths overall. Mortality within 96 hours of study enrolment appeared to be related to the original reason for emergency admission to the hospital, while all later events appeared to be related to co-morbidities.
“The real-world results from RE-VERSE AD™ are extremely encouraging and demonstrate how idarucizumab* can support patient management during emergency situations,” said Professor Jörg Kreuzer, Vice President Medicine Therapeutic Area Cardiovascular, Boehringer Ingelheim. “The study is ongoing. We look forward to gaining further understanding of the potential of idarucizumab* as yet another breakthrough in anticoagulant therapy for advancing care of patients who require urgent reversal of the anticoagulant effect of dabigatran.”
* Idarucizumab is the recommended International Nonproprietary Name (INN). Idarucizumab is an investigational drug, which has not been approved for clinical use, and further safety and efficacy testing will be required.
This press release is issued from our Corporate Headquarters in Ingelheim, Germany and is intended to provide information about our global business. 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.
~ENDS~
Please click on the link below for ‘Notes to Editors’ and ‘References’: http://www.boehringer-ingelheim.com/news/news_releases/press_releases/2015/22_june_2015_dabigatranetexilate.html
Contacts
Boehringer Ingelheim GmbH
Friederike Middeke
Phone: +49 6132 – 77 141575
Fax: +49 6132 – 77 6601
E-mail: press@boehringer-ingelheim.com
Twitter: http://twitter.com/Boehringer
or
More information
www.boehringer-ingelheim.com
Permalink: http://me-newswire.net/news/14978/en
First patient study data show that idarucizumab* immediately reverses dabigatran within minutes in patients requiring urgent procedures or with serious bleeding complications1,2
Interim analysis from RE-VERSE AD™, the first study investigating the effect of a specific reversal agent to a NOAC with patients in a real-world setting
Data are published in the New England Journal of Medicine and presented at the ISTH 2015 Congress1,2
(BUSINESS WIRE)-- Results from an interim analysis of the Phase III RE-VERSE AD™ patient study demonstrate that 5 g of idarucizumab* immediately reversed the anticoagulant effect of dabigatran (Pradaxa®) in patients requiring urgent anticoagulant reversal. No safety concerns relating to idarucizumab* were identified. The results have been simultaneously published in the New England Journal of Medicine (NEJM) and presented today at the International Society of Thrombosis and Haemostasis 2015 Congress in Toronto, Canada.1,2
“The interim analysis from RE-VERSE AD™ is important for healthcare professionals as it provides the first insights into the effect of a specific reversal agent to a non-vitamin K antagonist oral anticoagulant during real-world emergency situations,” said Dr. Charles Pollack, Professor of Emergency Medicine at the Perelman School of Medicine, University of Pennsylvania in Philadelphia, USA, and lead investigator of the patient study. “As observed in earlier research in volunteers, idarucizumab* reversed the anticoagulant effect of dabigatran in patients completely within minutes, even in those rare critical care situations studied in RE-VERSE AD™. These data demonstrate that use of idarucizumab* can help physicians focus on other vital aspects of emergency management beyond anticoagulant reversal in dabigatran-treated patients.”
RE-VERSE AD™ is designed to evaluate the types of patients and real-world situations healthcare professionals may see in emergency settings.1,3 The broad inclusion criteria ensure that even the most severely ill or injured patients (e.g. patients with sepsis or a severe intracranial haemorrhage), who require urgent reversal of dabigatran, may be enrolled in the study.1,3 Patients were categorised into two groups – (A) patients with uncontrolled or life-threatening bleeding complications, e.g. intracranial haemorrhage or severe trauma after a car accident (Group A, n= 51), or (B) patients requiring emergency surgery or an invasive procedure, e.g. surgery for an open fracture after a fall (Group B, n=39).1,3 The primary endpoint of the study is the degree of reversal of the anticoagulant effect of dabigatran achieved by 5 g idarucizumab* within 4 hours measured by diluted thrombin time (dTT) and ecarin clotting time (ECT).3
The interim analysis from RE-VERSE AD™ included data from 90 patients in emergency settings who were taking dabigatran and required reversal. Of the 81 patients that presented with elevated anticoagulation levels at baseline as measured with ECT, results showed:1
The study met its primary endpoint, achieving 100 per cent maximum reversal as median value across all patients
Reversal was evident immediately after administration of the first vial of idarucizumab* and was complete in all but 1 patient
After 4 and 12 hours, laboratory tests showed normal coagulation levels in almost 90 per cent of patients
Normal blood clotting (haemostasis) during surgery was reported in 92 per cent of the patients that required surgery or invasive procedures
There was no signal of a pro-coagulant effect following administration of idarucizumab*
Thrombotic events occurred in five patients, none of whom were receiving antithrombotic therapy at the time of the event
There were 18 deaths overall. Mortality within 96 hours of study enrolment appeared to be related to the original reason for emergency admission to the hospital, while all later events appeared to be related to co-morbidities.
“The real-world results from RE-VERSE AD™ are extremely encouraging and demonstrate how idarucizumab* can support patient management during emergency situations,” said Professor Jörg Kreuzer, Vice President Medicine Therapeutic Area Cardiovascular, Boehringer Ingelheim. “The study is ongoing. We look forward to gaining further understanding of the potential of idarucizumab* as yet another breakthrough in anticoagulant therapy for advancing care of patients who require urgent reversal of the anticoagulant effect of dabigatran.”
* Idarucizumab is the recommended International Nonproprietary Name (INN). Idarucizumab is an investigational drug, which has not been approved for clinical use, and further safety and efficacy testing will be required.
This press release is issued from our Corporate Headquarters in Ingelheim, Germany and is intended to provide information about our global business. 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.
~ENDS~
Please click on the link below for ‘Notes to Editors’ and ‘References’: http://www.boehringer-ingelheim.com/news/news_releases/press_releases/2015/22_june_2015_dabigatranetexilate.html
Contacts
Boehringer Ingelheim GmbH
Friederike Middeke
Phone: +49 6132 – 77 141575
Fax: +49 6132 – 77 6601
E-mail: press@boehringer-ingelheim.com
Twitter: http://twitter.com/Boehringer
or
More information
www.boehringer-ingelheim.com
Permalink: http://me-newswire.net/news/14978/en
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