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Updated: Feb 12, 2026

A Kinetic Fluorescence-based Ca2+ Mobilization Assay to Identify G Protein-coupled Receptor Agonists, Antagonists, and Allosteric Modulators
Published on: February 20, 2018
Elinogrel, an orally and intravenously available ADP-receptor antagonist
Insights
Standard antiplatelet drugs like clopidogrel show variable effectiveness. Elinogrel, a new drug, offers more consistent platelet inhibition, potentially improving outcomes for patients with acute coronary syndrome or after coronary intervention.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Aspirin and clopidogrel are standard antiplatelet therapies post-coronary intervention or acute coronary syndrome.
- High interindividual variability in response to clopidogrel affects up to 44% of patients, impacting treatment efficacy.
- Platelet function testing (PFT) can identify high-risk patients, but PFT-guided therapy has not shown improved prognostic outcomes in recent trials.
Purpose of the Study:
- To review the investigational drug elinogrel as a personalized antiplatelet therapy.
- To highlight elinogrel's potential to overcome poor response to standard antiplatelet agents.
Main Methods:
- Review of existing literature on antiplatelet therapy and elinogrel.
- Comparison of elinogrel's pharmacological profile and clinical effects with clopidogrel.
Main Results:
- Elinogrel is a novel, reversible ADP-receptor antagonist available in oral and intravenous forms.
- Elinogrel demonstrates more rapid, less variable, and more complete platelet inhibition compared to clopidogrel.
- Elinogrel administration did not significantly increase bleeding complications.
Conclusions:
- Elinogrel presents a promising alternative for personalized antiplatelet therapy.
- The drug's efficacy and safety profile suggest advantages over clopidogrel in specific patient populations.
- Further investigation into elinogrel's role in preventing ischemic events is warranted.
Abstract:
The antiplatelet therapy with aspirin and the ADP-receptor blocker clopidogrel is currently the standard medication after coronary intervention or after acute coronary syndrome to prevent recurrent ischemic events and reduce mortality. However, high interindividual response variability to antiplatelet treatment is described in up to 44% of treated patients. A poor response to clopidogrel is caused by multifactorial mechanisms. Individual risk assessment including platelet function testing (PFT) can help to identify high risk patients, although recent randomized trials to investigate effects of PFT-guided therapy have failed to detect an impact on prognostic outcome. Poor response to standard antiplatelet agents can be overcome by switching to alternate substances. Elinogrel is a novel competitive, reversible ADP-receptor antagonist available in oral and intravenous formulation. Additional treatment with elinogrel showed advantages over clopidogrel, including more rapid, less variable, and more complete inhibition of platelet function without significantly increased bleeding complications. This review gives an overview over the investigational drug elinogrel for use in a personalized antiplatelet approach.
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