In order to bring you the best possible user experience, this site uses Javascript. If you are seeing this message, it is likely that the Javascript option in your browser is disabled. For optimal viewing of this site, please ensure that Javascript is enabled for your browser.
Did you know that your browser is out of date? To get the best experience using our website we recommend that you upgrade to a newer version. Learn more.

Phase 2 safety and tolerability data on elinogrel, a novel antiplatelet agent, in non-urgent PCI

Hotline II: Embargoed for release: Monday 30 August 2010 0800hrs

Stockholm, Sweden, 30 August: Phase 2 trial results for elinogrel, a novel antiplatelet agent available in both intravenous and oral formulations, were presented here today.

The study, INNOVATE PCI, was a randomised dose-ranging trial that compared elinogrel, a P2Y12 inhibitor which in its IV form provides rapid, reversible platelet inhibition, with clopidogrel in 652 patients undergoing non-urgent PCI. Current P2Y12 antagonists are taken orally and require several hours to reach maximal platelet inhibition. The most widely used P2Y12 inhibitor is clopidogrel, which has significant variability in response (and indeed a lack of response in some patients).

According to the INNOVATE PCI trial, elinogrel provides a more potent antiplatelet effect in both the IV and oral forms; however, this immediate platelet inhibition has yet to be translated into a reduction in hard clinical endpoints.

Patients were initially assigned pre-PCI to clopidogrel 300 or 600 mg followed by 75 mg/day, or to elinogrel 80 mg IV bolus followed by 50, 100, or 150 mg oral elinogrel twice daily. The Data & Safety Monitoring Committee recommended discontinuation of enrolment into the 50 mg oral dose arm and increasing elinogrel IV dose to 120 mg; 590 patients were followed for 60 days, and 328 for 120 days.

While the study was not powered to determine efficacy, principal investigator Dr Sunil Rao from the Duke Clinical Research Institute, Durham, USA, said the results now provide a basis for further exploration of elinogrel in larger trials examining clinical endpoints. Rao explained that a pharmacodynamic sub-study provided two key findings as the basis for this further research: elinogrel appeared to be more potent than clopidogrel in platelet inhibition and inhibition appeared greater at higher doses.

“While clopidogrel is a well established and effective therapy," said Rao, "it doesn’t work for all patients, so it is important that we explore alternatives to improve efficacy help prevent serious complications.”



* Clopidogrel is recommended for treatment of patients with acute coronary syndrome and/or PCI. However, the delayed onset of effect and varied response are associated with a raised risk of stent thrombosis. The molecular target of clopidogrel and newer antiplatelet agents is the P2Y12 receptor, which is the main platelet receptor responsible platelet aggregation.

Notes to editor

About the European Society of Cardiology
The European Society of Cardiology (ESC) represents more than 62,000 cardiology professionals across Europe and the Mediterranean. Its mission is to reduce the burden of cardiovascular disease in Europe.

About ESC Congress 2010
ESC Congress 2010 will take place from 28 August to 1 September at the Stockholmsmässan, Stockholm. Information on the scientific programme is available at More information on ESC Congress 2010 is available from the ESC's press office at

This press release accompanies both a presentation and an ESC press conference given at the ESC Congress 2010. The press release has been written and/or edited by the ESC from information provided by the investigator and does not necessarily reflect the opinion of the European Society of Cardiology. The content of the press release has been approved by the investigator.