IUPAC_name = N 6 -(aminoiminomethyl)-N 2 -(3-mercapto-1-oxopropyl-L-lysylglycyl-L-a-aspartyl-L- tryptophyl-L -prolyl-L-cysteinamide

width = 400
CAS_number = 188627-80-7
ATC_prefix = B01
ATC_suffix = AC16
ATC_supplemental =
PubChem = 123610
DrugBank = BTD00063
C = 35 | H = 49 | N = 11 | O = 9 | S = 2
molecular_weight = 831.96 g/mol
bioavailability = n/a
protein_bound = ~25%
metabolism =
elimination_half-life = ~2.5 hours
excretion = Renal
licence_EU = Integrilin
licence_US = Eptifibatide
pregnancy_US = B
legal_UK = POM
legal_US = Rx-only
legal_status =
routes_of_administration = IV only

Eptifibatide (Integrilin, Millennium Pharmaceuticals, also co-promoted by Schering-Plough/Essex), is an antiplatelet drug that selectively blocks the platelet glycoprotein IIb/IIIa receptor. Eptifibatide is a cyclic heptapeptide derived from a protein found in the venom of the southeastern pygmy rattlesnake ("Sistrurus miliarus barbouri"). It belongs to the class of the so called arginin-glycin-aspartat-mimetics and reversibly binds to platelets. Eptifibatide has a short half-life. The drug is the third inhibitor of GPIIb/IIIa that has found broad acceptance after the specific antibody abciximab and the non-peptide tirofiban entered the global market.

Integrilin is sold in two strengthes, globally: vials containing 2 mg/ml (20 mg totally) and 0.75 mg/ml (75 mg totally). A third strength is sold in the US: 100 ml vials containing 2 mg/ml (200 mg totally).


Eptifibatide is used to reduce the risk of acute cardiac ischemic events (death and/or myocardial infarction) in patients with unstable angina or non-ST-segment-elevation (e.g., non-Q-wave) myocardial infarction (i.e., non-ST-segment elevation acute coronary syndromes) both in patients who are to receive non surgery (conservative) medical treatment and those undergoing percutaneous coronary intervention (PCI).

The drug is always applied together with aspirin or clopidogrel and (low molecular weight or unfractionated) heparin. Additionally, the usual supportive treatment consisting of applications of nitrates, beta-blockers, lidocaine, opioid analgesics and/or benzodiazepines should be employeed as indicated. Angiographic evaluation and other intensive diagnostic procedures may be considered a first line task before initiating therapy with eptifibatide.

The drug should exclusively be used in hospitalized patients both because of the serious degree of patients' illness and because of the possible side-effects of eptifibatide.

Contraindications and precautions

* Thrombocytopenia : The drug is contraindicated in patients with platelet counts of less than 100,000 because no clinical experience exists regarding such patients.
* Renal insufficiency : Eptifibatide undergoes renal elimination. In such patients with renal insufficiency where a glycoprotein IIb/IIIa inhibitor is likely to provide benefit, Abciximab (trade name: Reopro) is an alternative medication.
* Current bleeding tendencies or abnormally prolonged coagulation parameters observed within 30 days before starting therapy with eptifibatide is intended.
* Coagulation parameters such as ACT, aPTT, TT, and PT should be followed closely during therapy and afterwards.
* Allergy to eptifibatide and/or other ingredients.
* Severe, uncontrolled hypertension.
* Pregnancy : No experience exists. Pregnant patients should be treated only when clearly needed.
* Lactation : No human data exists. Breast-feeding should be avoided during treatment in order to prevent damage to the newborn.
* Geriatric patients : No differences in side effects compared with younger patients have been seen. Nevertheless, geriatric patients should be very closely observed for bleeding and other side-effects.
* Pediatric patients : Eptifibatide is not indicated in patients below 18 years of age, because no experience exists.

ide effects

It should be noticed that all patients receiving eptifibatide were seriously ill and most of them were concomitantly treated with other drugs known to have the potential to cause significant side effects. Therefore, not all side effects listed as follows may be attributable to eptifibatide treatment alone:

The major adverse event in the PURSUIT study was severe bleeding. Bleeding occurred as well at sites of clinical intervention (local sites) as at other sites (systemically) like urogenital bleedings. Sometimes, these events were severe enough to require transfusion of blood or plasma concentrates to stop bleeding and counteract anemia. Severe bleedings occurred in 4.4 and 4.7 % of patients respectively depending on the infusion rate (0.5 µg/kg and minute vs. 0.75 µg/kg and minute). A few cases of death due to severe bleeding events attributable to drug therapy were reported. No cases of hemorrhagic stroke were seen. Thrombocytopenia of unknown origin (allergic reaction?) was also noticed in 0.2 % of patients.

Additionally, hypotension was seen frequently (6 %). Cardiovascular failure was also frequent (2 %) as were serious arrhythmias (ventricular fibrillation 1.5 %, atrial fibrillation 6 %). Severe allergic (anaphylactic) reactions occurred in almost 0.2 % of patients. These reactions can be life-threatening and may be due to the peptide character of eptifibatide. Other side effects were rare and mild in nature and may not be connected to eptifibatide therapy.

Dosage regime

The recommended adult dosage is an i.v. loading dose of 180 µg/kg over 1 to 2 minutes immediately after diagnosis, followed by continuous i.v.-infusion of 2 µg/kg per minute until either hospital discharge or initiation of coronary artery bypass grafting, or for up to 72 hours. At least 4 hours before discharge all local or systemic bleedings should have been controlled and terminated.

tudy results

Eptifibatide was licensed due to the positive results of the so called PURSUIT study encompassing 10,948 patients. In this study all patients had suffered either unstable angina or a non-ST-segment-elevation myocardial infarction. Significantly fewer patients developed a myocardial infarction under therapy with eptifibatide. Death rates showed a tendency in favour of eptifibatide, but this superiority was not statistically significant.

Additional information

Sometimes the treating physicians require the patient after discharge from hospital to continue treatment with aspirin or clopidrogel or heparin for a few weeks, some months or even for life (as usually is the case with aspirin) to prevent recurrence of symptoms, development of myocardial infarction and/or death related to cardiovascular disease. These advises should be adhered to strictly.Eptifibatide is one of very many antiplatelet drugs [http://www.healthvalue.net/antiplateletdrugs.html] that all have different consequences on the platelet's activity.


Integrilin was invented by Robert M. Scarborough [http://www.sfgate.com/cgi-bin/article.cgi?file=/c/a/2006/08/01/BAGFLK8UD41.DTL] and David Phillips, at COR Therapeutics, Inc. in South San Francisco, CA. The company was acquired by Millennium pharmaceuticals,Inc,. of MA in 2001. David Phillips is also the original discoverer of GPIIb/IIIa on the platelets ( [http://www.neurology.org/cgi/content/abstract/57/suppl_2/S12] ). Robert Scarborough, a medicinal chemist, is also the discoverer of Natrecor (Nesiritide), sold by Johnson and Johnson.


* AHFS Database Online
* Arzneimittel Datenbank (in German)
* http://www.pharmazeutische-zeitung.de/index.php?id=352&type=0 (in German)
* http://www.chemsoc.org/chembytes/ezine/1999/berressem_apr99.htm (information on the biological origin of eptifibatide)

ee also

*Glycoprotein IIb/IIIa inhibitors

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