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Updated: Aug 17, 2026

Targeted Antibody Blocking by a Dual-Functional Conjugate of Antigenic Peptide and Fc-III Mimetics (DCAF)
Published on: September 17, 2019
Abciximab (Reopro): a clinically effective glycoprotein IIb/IIIa receptor blocker
1Cardiothoracic Division, South Cleveland Hospital, Middlesbrough, Marton Road, TS4 3BW, UK.
Insights
New therapies like abciximab are improving outcomes for acute coronary syndromes. This glycoprotein IIb/IIIa receptor blocker effectively reduces myocardial infarction and revascularization needs in high-risk patients undergoing percutaneous transluminal coronary angioplasty.
Area of Science:
- Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Acute coronary syndromes (ACS) are a leading cause of mortality worldwide.
- Current treatments for ACS, including myocardial infarction (MI) and unstable angina (UA), have limitations.
- Novel therapeutic strategies are needed to further reduce ACS incidence and risk.
Purpose of the Study:
- To evaluate the efficacy of new therapeutic agents in managing ACS and percutaneous transluminal coronary angioplasty (PTCA).
- To specifically assess the role of glycoprotein IIb/IIIa receptor blockers, particularly abciximab, in ACS and PTCA.
Main Methods:
- Review of clinical studies evaluating new agents for ACS and PTCA.
- Focus on abciximab, a glycoprotein IIb/IIIa receptor antagonist.
- Analysis of data regarding reduction in ischemic complications, MI, and repeat revascularization.
Main Results:
- Abciximab demonstrated clear efficacy in reducing acute ischemic complications in high-risk patients undergoing PTCA.
- It significantly reduced the frequency of myocardial infarction and the need for repeat revascularization.
- Both short- and long-term efficacy of abciximab were observed, distinguishing it from other agents in its class.
Conclusions:
- Abciximab is a potent platelet aggregation inhibitor with proven benefits in PTCA.
- Further research is ongoing to explore its role in intracoronary stent implantation and early management of unstable angina.
- Abciximab shows promise in enhancing the efficacy of thrombolytic agents in ACS management.
Abstract:
Acute coronary syndromes are responsible for the deaths of tens of thousands of patients every year. Rupture of coronary atheromatous plaques with resultant luminal thrombosis is the cause in most cases. Although great steps forward have been taken in the management of acute myocardial infarction (MI) and unstable angina (UA), new therapeutic strategies are required to reduce further the incidence and risk of these events. At present, aspirin, nitrates and heparin are the conventional treatments for unstable angina. Aspirin, in combination with a thrombolytic agent or with percutaneous transluminal coronary angioplasty (PTCA), has been shown to be effective in reducing mortality in acute MI. Heparin is conventionally used in all PTCA procedures, whereas its efficacy in enhancing the therapeutic role of thrombolytic agents remains uncertain and may depend on the thrombolytic agent used. PTCA, which is also an effective therapy for stable angina, can be complicated by intimal dissection and thrombosis in a minority of cases, with vessel restenosis leading to recurrent symptoms in approximately 30% of cases. A number of new agents are being evaluated in both acute coronary syndromes and PTCA. These can be classified as adenosine diphosphate (ADP) receptor antagonists, Factor Xa inhibitors (low-molecular weight heparin [LMWH], direct thrombin inhibitors, new thrombolytic agents and glycoprotein IIb/IIIa receptor blockers. Of the latter, the most studied is abciximab, the Fab fragment of the chimeric monoclonal antibody, 7E3. This is a potent inhibitor of platelet aggregation. Four major clinical studies of PTCA in high-risk patients have demonstrated clear efficacy of abciximab in reducing acute ischaemic complications, mainly by reducing the frequency of MI and the need for repeat revascularisation. Unlike other glycoprotein IIb/IIIa receptor blockers, both short- and long-term efficacy have been demonstrated. Its impact on the rate of restenosis after PTCA is unclear. Abciximab's role in an era of intracoronary stent implantation is undergoing further study (with encouraging early results). Its role in other situations, such as the early (non-angioplasty) management of unstable angina and its ability to enhance the efficacy of thrombolytic agents, is under active investigation.
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