Prescription Drugs

CLINICAL PHARMACOLOGY Mechanism Of Action Bivalirudin directly inhibits thrombin by specifically binding both to the catalytic site and to the anionbinding exosite of circulating and clot-bound thrombin. Thrombin is a serine proteinase that plays a central role in the thrombotic process, acting to cleave fibrinogen into fibrin monomers and to activate Factor XIII to Factor XIIIa, allowing fibrin to develop a covalently cross-linked framework which stabilizes the thrombus; thrombin also activates Factors V and VIII, promoting further thrombin generation, and activates platelets, stimulating aggregation and granule release. The binding of bivalirudin to thrombin is reversible as thrombin slowly cleaves the bivalirudin-Arg3-Pro4 bond, resulting in recovery of thrombin active site functions. In in vitro studies, bivalirudin inhibited both soluble (free) and clot-bound thrombin, was not neutralized by products of the platelet release reaction, and prolonged the activated partial thromboplastin time (aPTT), thrombin time (TT), and prothrombin time (PT) of normal human plasma in a concentrationdependent manner. The clinical relevance of these findings is unknown. Pharmacodynamics In healthy volunteers and patients (with ≥70% vessel occlusion undergoing routine PTCA), bivalirudin exhibited dose- and concentration-dependent anticoagulant activity as evidenced by prolongation of the ACT, aPTT, PT, and TT. Intravenous administration of bivalirudin produces an immediate anticoagulant effect. Coagulation times return to baseline approximately 1 hour following cessation of bivalirudin administration. In 291 patients with ≥70% vessel occlusion undergoing routine PTCA, a positive correlation was observed between the dose of bivalirudin and the proportion of patients achieving ACT values of 300 sec or 350 sec. At a bivalirudin dose of 1 mg/kg IV bolus plus 2.5 mg/kg/h IV infusion for 4 hours, followed by 0.2 mg/kg/h, all patients reached maximal ACT values >300 sec. Pharmacokinetics Bivalirudin exhibits linear pharmacokinetics following IV administration to patients undergoing PTCA. In these patients, a mean steady state bivalirudin concentration of 12.3 ± 1.7 mcg/mL is achieved following an IV bolus of 1 mg/kg and a 4-hour 2.5 mg/kg/h IV infusion. Bivalirudin does not bind to plasma proteins (other than thrombin) or to red blood cells. Bivalirudin is cleared from plasma by a combination of renal mechanisms and proteolytic cleavage, with a half-life in patients with normal renal function of 25 min. The disposition of bivalirudin was studied in PTCA patients with mild, moderate, and severe renal impairment. Drug elimination was related to glomerular filtration rate (GFR). Total body clearance was similar for patients with normal renal function and with mild renal impairment (60 to 89 mL/min). Clearance was reduced in patients with moderate and severe renal impairment and in dialysis-dependent patients (see Table 6 for pharmacokinetic parameters). Bivalirudin is hemodialyzable, with approximately 25% cleared by hemodialysis. Table 6: PK Parameters in Patients with Renal Impairment* Renal Function (GFR, mL/min) Clearance(mL/min/kg) Half-life (min) Normal renal function (≥90 mL/min) 3.4 25 Mild renal impairment (60 to 89 mL/min) 3.4 22 Moderate renal impairment (30 to 59 mL/min) 2.7 34 Severe renal impairment (10 to 29 mL/min) 2.8 57 Dialysis-dependent patients (off dialysis) 1.0 3.5 hours *The ACT should be monitored in renally-impaired patients. Clinical Studies PCI/PTCA Bivalirudin has been evaluated in five randomized, controlled interventional cardiology trials reporting 11,422 patients. Stents were deployed in 6,062 of the patients in these trials – mainly in trials performed since 1995. Percutaneous transluminal coronary angioplasty, atherectomy or other procedures were performed in the remaining patients. REPLACE-2 Trial This was a randomized, double-blind, multicenter study reporting 6,002 (intent-to-treat) patients undergoing PCI. Patients were randomized to treatment with bivalirudin with the “provisional” use of platelet glycoprotein IIb/IIIa inhibitor (GPI) or heparin plus planned use of GPI. GPIs were added on a “provisional” basis to patients who were randomized to bivalirudin in the following circumstances: decreased TIMI flow (0 to 2) or slow reflow; dissection with decreased flow; new or suspected thrombus; persistent residual stenosis; distal embolization; unplanned stent; suboptimal stenting; side branch closure; abrupt closure; clinical instability; and prolonged ischemia. During the study, one or more of these circumstances occurred in 10.9% of patients in the bivalirudin with provisional GPI arm. GPIs were administered to 7.2% of patients in the bivalirudin with provisional GPI arm (66.8% of eligible patients). Patients ranged in age from 25 to 95 years (median, 63); weight ranged from 35 to 199 kg (median 85.5); 74.4% were male and 25.6% were female. Indications for PCI included unstable angina (35% of patients), myocardial infarction within 7 days prior to intervention (8% of patients), stable angina (25%), positive ischemic stress test (24%), and other not specified indications (8%). Stents were deployed in 85% of patients. Ninety-nine percent of patients received aspirin and 86% received thienopyridines prior to study treatment. Bivalirudin was administered as a 0.75 mg/kg bolus followed by a 1.75 mg/kg/h infusion for the duration of the procedure. The activated clotting time (ACT – measured by a Hemochron® device) was measured 5 min after the first bolus of study medication. If the ACT was < 225 seconds, an additional bolus of 0.3 mg/kg was given. At investigator discretion, the infusion could be continued following the procedure for up to 4 hours. The median infusion duration was 44 min. Heparin was administered as a 65 U/kg bolus. The activated clotting time (ACT – measured by a Hemochron® device) was measured 5 min after the first bolus of study medication. If the ACT was < 225 seconds, an additional bolus of 20 units/kg was given. GPIs (either abciximab or eptifibatide) were given according to manufacturers’ instructions. Both randomized groups could be given “provisional” treatments during the PCI at investigator discretion, but under double-blind conditions. “Provisional” treatment with GPI was requested in 5.2% of patients randomized to heparin plus GPI (they were given placebo) and 7.2% patients randomized to bivalirudin with provisional GPI (they were given abciximab or eptifibatide according to pre-randomization investigator choice and patient stratification). The percent of patients reaching protocol-specified levels of anticoagulation was greater in the bivalirudin with provisional GPI group than in the heparin plus GPI group. For patients randomized to bivalirudin with provisional GPI, the median 5 min ACT was 358 sec (interquartile range 320 to 400 sec) and the ACT was < 225 sec in 3%. For patients randomized to heparin plus GPI, the median 5 min ACT was 317 sec (interquartile range 263 to 373 sec) and the ACT was < 225 sec in 12%. At the end of the procedure, median ACT values were 334 sec (bivalirudin group) and 276 sec (heparin plus GPI group). For the composite endpoint of death, MI, or urgent revascularization adjudicated under double-blind conditions, the frequency was higher (7.6%) (95% confidence interval 6.7% to 8.6%) in the bivalirudin with “provisional” GPI arm when compared to the heparin plus GPI arm (7.1%) (95% confidence interval 6.1% to 8.0%). However, major hemorrhage was reported significantly less frequently in the bivalirudin with provisional GPI arm (2.4%) compared to the heparin plus GPI arm (4.1%). Study outcomes are shown in Table 7. Table 7: Incidences of Clinical Endpoints at 30 Days for REPLACE-2, a Randomized Doubleblind Clinical Trial Intent-to-treat Population Bivalirudin with “Provisional” GPI (n=2,994) Heparin + GPI (n=3,008) Efficacy Endpoints Death, MI, or urgent revascularization 7.6% 7.1% Death 0.2% 0.4% MI 7.0% 6.2% Urgent revascularization 1.2% 1.4% Safety Endpoint Major hemorrhage1,2 2.4% 4.1% 1Defined as intracranial bleeding, retroperitoneal bleeding, a transfusion of >2 units of blood/blood products, a fall in Hgb >4 g/dL, whether or not bleeding site is identified, spontaneous or nonspontaneous blood loss with a decrease in Hgb >3 g/dL. 2p-value <0.001 between groups. At 12 months’ follow-up, mortality was 1.9% among patients randomized to bivalirudin with “provisional” GPIs and 2.5% among patients randomized to heparin plus GPI. Bivalirudin Angioplasty Trial (BAT) Bivalirudin was evaluated in patients with unstable angina undergoing PTCA in two randomized, doubleblind, multicenter studies with identical protocols. Patients must have had unstable angina defined as: (1) a new onset of severe or accelerated angina or rest pain within the month prior to study entry or (2) angina or ischemic rest pain which developed between four hours and two weeks after an acute myocardial infarction (MI). Overall, 4,312 patients with unstable angina, including 741 (17%) patients with post-MI angina, were treated in a 1:1 randomized fashion with bivalirudin or heparin. Patients ranged in age from 29 to 90 (median 63) years, their weight was a median of 80 kg (39 to 120 kg), 68% were male, and 91% were Caucasian. Twenty-three percent of patients were treated with heparin within one hour prior to randomization. All patients were administered aspirin 300 to 325 mg prior to PTCA and daily thereafter. Patients randomized to bivalirudin were started on an intravenous infusion of bivalirudin (2.5 mg/kg/h). Within 5 min after starting the infusion, and prior to PTCA, a 1 mg/kg loading dose was administered as an intravenous bolus. The infusion was continued for 4 hours, then the infusion was changed under double-blinded conditions to bivalirudin (0.2 mg/kg/h) for up to an additional 20 hours (patients received this infusion for an average of 14 hours). The ACT was checked at 5 min and at 45 min following commencement. If on either occasion the ACT was <350 sec, an additional double-blinded bolus of placebo was administered. The bivalirudin dose was not titrated to ACT. Median ACT values were: ACT in sec (5th percentile to 95th percentile): 345 sec (240 to 595 sec) at 5 min and 346 sec (range 269 to 583 sec) at 45 min after initiation of dosing. Patients randomized to heparin were given a loading dose (175 IU/kg) as an intravenous bolus 5 min before the planned procedure, with immediate commencement of an infusion of heparin (15 IU/kg/h). The infusion was continued for 4 hours. After 4 hours of infusion, the heparin infusion was changed under doubleblinded conditions to heparin (15 IU/kg/h) for up to 20 additional hours. The ACT was checked at 5 min and at 45 min following commencement. If on either occasion the ACT was <350 sec, an additional double-blind bolus of heparin (60 IU/kg) was administered. Once the target ACT was achieved for heparin patients, no further ACT measurements were performed. All ACTs were determined with the Hemochron® device. The protocol allowed use of open-label heparin at the discretion of the investigator after discontinuation of blinded study medication, whether or not an endpoint event (procedural failure) had occurred. The use of open-label heparin was similar between bivalirudin and heparin treatment groups (about 20% in both groups). The studies were designed to demonstrate the safety and efficacy of bivalirudin in patients undergoing PTCA as a treatment for unstable angina as compared with a control group of similar patients receiving heparin during and up to 24 hours after initiation of PTCA. The primary protocol endpoint was a composite endpoint called procedural failure, which included both clinical and angiographic elements measured during hospitalization. The clinical elements were: the occurrence of death, MI, or urgent revascularization, adjudicated under double-blind conditions. The angiographic elements were: impending or abrupt vessel closure. The protocol-specified safety endpoint was major hemorrhage. The median duration of hospitalization was 4 days for both the bivalirudin and the heparin treatment groups. The rates of procedural failure were similar in the bivalirudin and heparin treatment groups. Study outcomes are shown in Table 8. Table 8: Incidences of In-hospital Clinical Endpoints in BAT Trial Occurring within 7 Days All Patients Bivalirudin (n=2,161) Heparin (n=2,151) Efficacy Endpoints Procedural failure1 7.9% 9.3% Death, MI, revascularization 6.2% 7.9% Death 0.2% 0.2% MI2 3.3% 4.2% Revascularization3 4.2% 5.6% Safety Endpoint Major hemorrhage4 3.5% 9.3% 1The protocol-specified primary endpoint (a composite of death or MI or clinical deterioration of cardiac origin requiring revascularization or placement of an aortic balloon pump or angiographic evidence of abrupt vessel closure). 2Defined as: Q-wave MI; CK-MB elevation ≥2 x ULN, new ST- or T-wave abnormality, and chest pain ≥30 min; OR new LBBB with chest pain ≥30 min and/or elevated CK-MB enzymes; OR elevated CKMB and new ST- or T-wave abnormality without chest pain; OR elevated CK-MB. 3Defined as: any revascularization procedure, including angioplasty, CABG, stenting, or placement of an intra-aortic balloon pump. 4Defined as the occurrence of any of the following: intracranial bleeding, retroperitoneal bleeding, clinically overt bleeding with a decrease in Hgb ≥3 g/dL or leading to a transfusion of ≥2 units of blood. AT-BAT Trial This was a single-group open-label study which enrolled 51 patients with heparin-induced thrombocytopenia (HIT) or heparin-induced thrombocytopenia and thrombosis syndrome (HITTS) undergoing PCI. Evidence for the diagnosis of HIT/HITTS was based on a clinical history of a decrease of platelets in patients after heparin administration [new diagnosis or history of clinically suspected or objectively documented HIT/HITTS defined as either: 1) HIT: positive heparin-induced platelet aggregation (HIPA) or other functional assay where the platelet count has decreased to <100,000/mL (minimum 30% from prior to heparin), or has decreased to <150,000/mL (minimum 40% from prior to heparin), or has decreased as above within hours of receiving heparin in a patient with a recent, previous exposure to heparin; 2) HITTS: thrombocytopenia as above plus arterial or venous thrombosis diagnosed by physician examination/laboratory and/or appropriate imaging studies]. Patients ranged in age from 48 to 89 years (median 70); weight ranged from 42 to 123 kg (median 76); 50% were male and 50% were female. Bivalirudin was administered as either 1 mg/kg bolus followed by 2.5 mg/kg/h (high dose in 28 patients) or 0.75 mg/kg bolus followed by a 1.75 mg/kg/h infusion (lower dose in 25 patients) for up to 4 hours. Ninety-eight percent of patients received aspirin, 86% received clopidogrel and 19% received GPIs. The median ACT values at the time of device activation were 379 sec (high dose) and 317 sec (lower dose). Following the procedure, 48 of the 51 patients (94%) had TIMI grade 3 flow and stenosis <50%. One patient died during a bradycardic episode 46 hours after successful PCI, another patient required surgical revascularization, and one patient experienced no flow requiring a temporary intraaortic balloon. Two of the fifty-one patients with the diagnosis of HIT/HITTS developed thrombocytopenia after receiving bivalirudin and GPIs.

CLINICAL PHARMACOLOGY Mechanism Of Action Bivalirudin directly inhibits thrombin by specifically binding both to the catalytic site and to the anion-binding exosite of circulating and clot-bound thrombin. Thrombin is a serine proteinase that plays a central role in the thrombotic process, acting to cleave fibrinogen into fibrin monomers and to activate Factor XIII to Factor XIIIa, allowing fibrin to develop a covalently cross-linked framework which stabilizes the thrombus; thrombin also activates Factors V and VIII, promoting further thrombin generation, and activates platelets, stimulating aggregation and granule release. The binding of bivalirudin to thrombin is reversible as thrombin slowly cleaves the bivalirudin-Arg3-Pro4 bond, resulting in recovery of thrombin active site functions. In in vitro studies, bivalirudin inhibited both soluble (free) and clot-bound thrombin, was not neutralized by products of the platelet release reaction, and prolonged the activated partial thromboplastin time (aPTT), thrombin time (TT), and prothrombin time (PT) of normal human plasma in a concentration-dependent manner. The clinical relevance of these findings is unknown. Pharmacodynamics In healthy volunteers and patients (with ≥70% vessel occlusion undergoing routine PTCA), bivalirudin exhibited dose- and concentration-dependent anticoagulant activity as evidenced by prolongation of the ACT, aPTT, PT, and TT. Intravenous administration of bivalirudin produces an immediate anticoagulant effect. Coagulation times return to baseline approximately 1 hour following cessation of bivalirudin administration. In 291 patients with ≥70% vessel occlusion undergoing routine PTCA, a positive correlation was observed between the dose of bivalirudin and the proportion of patients achieving ACT values of 300 sec or 350 sec. At a bivalirudin dose of 1 mg/kg IV bolus plus 2.5 mg/kg/h IV infusion for 4 hours, followed by 0.2 mg/kg/h, all patients reached maximal ACT values >300 sec. Pharmacokinetics Bivalirudin exhibits linear pharmacokinetics following IV administration to patients undergoing PTCA. In these patients, a mean steady state bivalirudin concentration of 12.3 ± 1.7 mcg/mL is achieved following an IV bolus of 1 mg/kg and a 4-hour 2.5 mg/kg/h IV infusion. Bivalirudin does not bind to plasma proteins (other than thrombin) or to red blood cells. Bivalirudin is cleared from plasma by a combination of renal mechanisms and proteolytic cleavage, with a half-life in patients with normal renal function of 25 min. The disposition of bivalirudin was studied in PTCA patients with mild, moderate, and severe renal impairment. Drug elimination was related to glomerular filtration rate (GFR). Total body clearance was similar for patients with normal renal function and with mild renal impairment (60-89 mL/min). Clearance was reduced in patients with moderate and severe renal impairment and in dialysis-dependent patients (see Table 6 for pharmacokinetic parameters). Bivalirudin is hemodialyzable, with approximately 25% cleared by hemodialysis. Table 6: PK Parameters in Patients with Renal Impairment* Renal Function (GFR, mL/min) Clearance (mL/min/kg) Half-life (min) Normal renal function (≥90 mL/min) 3.4 25 Mild renal impairment (60-89 mL/min) 3.4 22 Moderate renal impairment (30-59 mL/min) 2.7 34 Severe renal impairment (10-29 mL/min) 2.8 57 Dialysis-dependent patients (off dialysis) 1.0 3.5 hours *The ACT should be monitored in renally-impaired patients Clinical Studies PCI/PTCA Angiomax has been evaluated in five randomized, controlled interventional cardiology trials reporting 11,422 patients. Stents were deployed in 6062 of the patients in these trials – mainly in trials performed since 1995. Percutaneous transluminal coronary angioplasty, atherectomy or other procedures were performed in the remaining patients. REPLACE-2 Trial This was a randomized, double-blind, multicenter study reporting 6002 (intent-to-treat) patients undergoing PCI. Patients were randomized to treatment with Angiomax with the “provisional” use of platelet glycoprotein IIb/IIIa inhibitor (GPI) or heparin plus planned use of GPI. GPIs were added on a “provisional” basis to patients who were randomized to Angiomax in the following circumstances: decreased TIMI flow (0 to 2) or slow reflow; dissection with decreased flow; new or suspected thrombus; persistent residual stenosis; distal embolization; unplanned stent; suboptimal stenting; side branch closure; abrupt closure; clinical instability; and prolonged ischemia. During the study, one or more of these circumstances occurred in 10.9% of patients in the Angiomax with provisional GPI arm. GPIs were administered to 7.2% of patients in the Angiomax with provisional GPI arm (66.8% of eligible patients). Patients ranged in age from 25-95 years (median, 63); weight ranged from 35-199 kg (median 85.5); 74.4% were male and 25.6% were female. Indications for PCI included unstable angina (35% of patients), myocardial infarction within 7 days prior to intervention (8% of patients), stable angina (25%), positive ischemic stress test (24%), and other not specified indications (8%). Stents were deployed in 85% of patients. Ninety-nine percent of patients received aspirin and 86% received thienopyridines prior to study treatment. Angiomax was administered as a 0.75 mg/kg bolus followed by a 1.75 mg/kg/h infusion for the duration of the procedure. The activated clotting time (ACT – measured by a Hemochron® device) was measured 5 min after the first bolus of study medication. If the ACT was <225 seconds, an additional bolus of 0.3 mg/kg was given. At investigator discretion, the infusion could be continued following the procedure for up to 4 hours. The median infusion duration was 44 min. Heparin was administered as a 65 U/kg bolus. The activated clotting time (ACT – measured by a Hemochron® device) was measured 5 min after the first bolus of study medication. If the ACT was <225 seconds, an additional bolus of 20 units/kg was given. GPIs (either abciximab or eptifibatide) were given according to manufacturers' instructions. Both randomized groups could be given “provisional” treatments during the PCI at investigator discretion, but under double-blind conditions. “Provisional” treatment with GPI was requested in 5.2% of patients randomized to heparin plus GPI (they were given placebo) and 7.2% patients randomized to Angiomax with provisional GPI (they were given abciximab or eptifibatide according to pre-randomization investigator choice and patient stratification). The percent of patients reaching protocol-specified levels of anticoagulation was greater in the Angiomax with provisional GPI group than in the heparin plus GPI group. For patients randomized to Angiomax with provisional GPI, the median 5 min ACT was 358 sec (interquartile range 320-400 sec) and the ACT was <225 sec in 3%. For patients randomized to heparin plus GPI, the median 5 min ACT was 317 sec (interquartile range 263-373 sec) and the ACT was <225 sec in 12%. At the end of the procedure, median ACT values were 334 sec (Angiomax group) and 276 sec (heparin plus GPI group). For the composite endpoint of death, MI, or urgent revascularization adjudicated under doubleblind conditions, the frequency was higher (7.6%)(95% confidence interval 6.7%-8.6%) in the Angiomax with “provisional” GPI arm when compared to the heparin plus GPI arm (7.1%)(95% confidence interval 6.1%-8.0%). However, major hemorrhage was reported significantly less frequently in the Angiomax with provisional GPI arm (2.4%) compared to the heparin plus GPI arm (4.1%). Study outcomes are shown in Table 7. Table 7: Incidences of Clinical Endpoints at 30 Days for REPLACE-2, a Randomized Double-blind Clinical Trial Intent-to-treat Population ANGIOMAX with “Provisional” GPI (n=2994) HEPARIN + GPI (n=3008) Efficacy Endpoints Death, MI, or urgent revascularization 7.6% 7.1% Death 0.2% 0.4% MI 7.0% 6.2% Urgent revascularization 1.2% 1.4% Safety Endpoint Major hemorrhage1,2 2.4% 4.1% 1 Defined as intracranial bleeding, retroperitoneal bleeding, a transfusion of ≥2 units of blood/blood products, a fall in Hgb >4 g/dL, whether or not bleeding site is identified, spontaneous or non-spontaneous blood loss with a decrease in Hgb >3 g/dL 2 p-value <0.001 between groups At 12 months' follow-up, mortality was 1.9% among patients randomized to Angiomax with “provisional” GPIs and 2.5% among patients randomized to heparin plus GPI. Bivalirudin Angioplasty Trial (BAT) Angiomax was evaluated in patients with unstable angina undergoing PTCA in two randomized, double-blind, multicenter studies with identical protocols. Patients must have had unstable angina defined as: (1) a new onset of severe or accelerated angina or rest pain within the month prior to study entry or (2) angina or ischemic rest pain which developed between four hours and two weeks after an acute myocardial infarction (MI). Overall, 4312 patients with unstable angina, including 741 (17%) patients with post-MI angina, were treated in a 1:1 randomized fashion with Angiomax or heparin. Patients ranged in age from 29-90 (median 63) years, their weight was a median of 80 kg (39-120 kg), 68% were male, and 91% were Caucasian. Twentythree percent of patients were treated with heparin within one hour prior to randomization. All patients were administered aspirin 300-325 mg prior to PTCA and daily thereafter. Patients randomized to Angiomax were started on an intravenous infusion of Angiomax (2.5 mg/kg/h). Within 5 min after starting the infusion, and prior to PTCA, a 1 mg/kg loading dose was administered as an intravenous bolus. The infusion was continued for 4 hours, then the infusion was changed under double-blinded conditions to Angiomax (0.2 mg/kg/h) for up to an additional 20 hours (patients received this infusion for an average of 14 hours). The ACT was checked at 5 min and at 45 min following commencement. If on either occasion the ACT was <350 sec, an additional double-blinded bolus of placebo was administered. The Angiomax dose was not titrated to ACT. Median ACT values were: ACT in sec (5th percentile-95th percentile): 345 sec (240-595 sec) at 5 min and 346 sec (range 269-583 sec) at 45 min after initiation of dosing. Patients randomized to heparin were given a loading dose (175 IU/kg) as an intravenous bolus 5 min before the planned procedure, with immediate commencement of an infusion of heparin (15 IU/kg/h). The infusion was continued for 4 hours. After 4 hours of infusion, the heparin infusion was changed under double-blinded conditions to heparin (15 IU/kg/h) for up to 20 additional hours. The ACT was checked at 5 min and at 45 min following commencement. If on either occasion the ACT was <350 sec, an additional double-blind bolus of heparin (60 IU/kg) was administered. Once the target ACT was achieved for heparin patients, no further ACT measurements were performed. All ACTs were determined with the Hemochron® device. The protocol allowed use of open-label heparin at the discretion of the investigator after discontinuation of blinded study medication, whether or not an endpoint event (procedural failure) had occurred. The use of open-label heparin was similar between Angiomax and heparin treatment groups (about 20% in both groups). The studies were designed to demonstrate the safety and efficacy of Angiomax in patients undergoing PTCA as a treatment for unstable angina as compared with a control group of similar patients receiving heparin during and up to 24 hours after initiation of PTCA. The primary protocol endpoint was a composite endpoint called procedural failure, which included both clinical and angiographic elements measured during hospitalization. The clinical elements were: the occurrence of death, MI, or urgent revascularization, adjudicated under double-blind conditions. The angiographic elements were: impending or abrupt vessel closure. The protocolspecified safety endpoint was major hemorrhage. The median duration of hospitalization was 4 days for both the Angiomax and the heparin treatment groups. The rates of procedural failure were similar in the Angiomax and heparin treatment groups. Study outcomes are shown in Table 8. Table 8: Incidences of In-hospital Clinical Endpoints in BAT Trial Occurring within 7 Days All Patients ANGIOMAX (n=2161) HEPARIN (n=2151) Efficacy Endpoints Procedural failure1 7.9% 9.3% Death, MI, revascularization 6.2% 7.9% Death 0.2% 0.2% MI2 3.3% 4.2% Revascularization3 4.2% 5.6% Safety Endpoint Major hemorrhage4 3.5% 9.3% 1 The protocol-specified primary endpoint (a composite of death or MI or clinical deterioration of cardiac origin requiring revascularization or placement of an aortic balloon pump or angiographic evidence of abrupt vessel closure). 2 Defined as: Q-wave MI; CK-MB elevation ≥2 x ULN, new ST- or T-wave abnormality, and chest pain ≥30 min; OR new LBBB with chest pain ≥30 min and/or elevated CK-MB enzymes; OR elevated CK-MB and new ST- or T-wave abnormality without chest pain; OR elevated CK-MB. 3 Defined as: any revascularization procedure, including angioplasty, CABG, stenting, or placement of an intraaortic balloon pump. 4 Defined as the occurrence of any of the following: intracranial bleeding, retroperitoneal bleeding, clinically overt bleeding with a decrease in Hgb ≥3 g/dL or leading to a transfusion of ≥2 units of blood. AT-BAT Trial This was a single-group open-label study which enrolled 51 patients with heparin-induced thrombocytopenia (HIT) or heparin induced thrombocytopenia and thrombosis syndrome (HITTS) undergoing PCI. Evidence for the diagnosis of HIT/HITTS was based on a clinical history of a decrease of platelets in patients after heparin administration [new diagnosis or history of clinically suspected or objectively documented HIT/HITTS defined as either: 1) HIT: positive heparin-induced platelet aggregation (HIPA) or other functional assay where the platelet count has decreased to <100,000/mL (minimum 30% from prior to heparin), or has decreased to <150,000/mL (minimum 40% from prior to heparin), or has decreased as above within hours of receiving heparin in a patient with a recent, previous exposure to heparin; 2) HITTS: thrombocytopenia as above plus arterial or venous thrombosis diagnosed by physician examination/laboratory and/or appropriate imaging studies]. Patients ranged in age from 48-89 years (median 70); weight ranged from 42-123 kg (median 76); 50% were male and 50% were female. Angiomax was administered as either 1 mg/kg bolus followed by 2.5 mg/kg/h (high dose in 28 patients) or 0.75 mg/kg bolus followed by a 1.75 mg/kg/h infusion (lower dose in 25 patients) for up to 4 hours. Ninety-eight percent of patients received aspirin, 86% received clopidogrel and 19% received GPIs. The median ACT values at the time of device activation were 379 sec (high dose) and 317 sec (lower dose). Following the procedure, 48 of the 51 patients (94%) had TIMI grade 3 flow and stenosis <50%. One patient died during a bradycardic episode 46 hours after successful PCI, another patient required surgical revascularization, and one patient experienced no flow requiring a temporary intra-aortic balloon. Two of the fifty-one patients with the diagnosis of HIT/HITTS developed thrombocytopenia after receiving Angiomax and GPIs.

BIVALIRUDIN (bivalirudin) Injection DESCRIPTION Bivalirudin for Injection contains bivalirudin which is a specific and reversible direct thrombin inhibitor. Bivalirudin is a synthetic, 20 amino acid peptide, with the chemical name of D-phenylalanyl- L-prolyl-L-arginyl-L-prolyl-glycyl-glycyl-glycyl-glycyl-L-asparagyl-glycyl-L-aspartyl-Lphenylalanyl- L-glutamyl-L-glutamyl-L-isoleucyl-L-prolyl-L-glutamyl-L-glutamyl-L-tyrosyl-Lleucine. The active pharmaceutical ingredient is in the form of bivalirudin trifluoroacetate as a white to off-white powder. The chemical name for bivalirudin trifluoroacetate is D-phenylalanyl-L-prolyl-Larginyl- L-prolyl-glycyl-glycyl-glycyl-glycyl-L-asparagyl-glycyl-L-aspartyl-L-phenylalanyl-Lglutamyl- L-glutamyl-L-isoleucyl-L-prolyl-L-glutamyl-L-glutamyl-L-tyrosyl-L-leucine trifluoroacetate (Figure 1). The molecular weight of bivalirudin is 2,180 daltons (anhydrous free base peptide). Figure 1. Structural formula for bivalirudin trifluoroacetate Bivalirudin for Injection is supplied as a sterile white lyophilized cake, in single-dose vials. Each vial contains 250 mg bivalirudin, equivalent to an average of 270 mg of bivalirudin trifluoroactetate*, 125 mg mannitol, and sodium hydroxide to adjust the pH to 5 to 6 (equivalent of approximately 12.5 mg sodium). When reconstituted with Sterile Water for Injection, the product yields a clear to opalescent, colorless to slightly yellow solution, pH 5 to 6. *The range of bivalirudin trifluoroacetate is 260 mg to 280 mg based on a range of trifluoroacetic acid composition of 1.0 to 2.2 equivalents.

Find Lowest Prices on ANGIOMAX® (bivalirudin) for Injection, for Intravenous Use DESCRIPTION Angiomax contains bivalirudin which is a specific and reversible direct thrombin inhibitor. Bivalirudin is a synthetic, 20 amino acid peptide, with the chemical name of D-phenylalanyl-Lprolyl- L-arginyl-L-prolyl-glycyl-glycyl-glycyl-glycyl-L-asparagyl-glycyl-L-aspartyl-Lphenylalanyl- L-glutamyl-L-glutamyl-L-isoleucyl-L-prolyl-L-glutamyl-L-glutamyl-L-tyrosyl-Lleucine. The active pharmaceutical ingredient is in the form of bivalirudin trifluoroacetate as a white to off-white powder. The chemical name for bivalirudin trifluoroacetate is D-phenylalanyl- L-prolyl-L-arginyl-L-prolyl-glycyl-glycyl-glycyl-glycyl-L-asparagyl-glycyl-L-aspartyl-Lphenylalanyl- L-glutamyl-L-glutamyl-L-isoleucyl-L-prolyl-L-glutamyl-L-glutamyl-L-tyrosyl-Lleucine trifluoroacetate (Figure 1). The molecular weight of bivalirudin is 2180 daltons (anhydrous free base peptide). Figure 1: Structure formula for bivalirudin trifluoroacetate Angiomax is supplied as a sterile white lyophilized cake, in single-dose vials. Each vial contains 250 mg bivalirudin, equivalent to an average of 275 mg of bivalirudin trifluoroactetate*, 125 mg mannitol, and sodium hydroxide to adjust the pH to 5-6 (equivalent of approximately 12.5 mg sodium). When reconstituted with Sterile Water for Injection, the product yields a clear to opalescent, colorless to slightly yellow solution, pH 5-6. *The range of bivalirudin trifluoroacetate is 270 mg to 280 mg based on a range of trifluoroacetic acid composition of 1.7 to 2.6 equivalents.

INDICATIONS Percutaneous Transluminal Coronary Angioplasty (PTCA) Bivalirudin for Injection is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA). Percutaneous Coronary Intervention (PCI) Bivalirudin for Injection with provisional use of glycoprotein IIb/IIIa inhibitor (GPI) as listed in the REPLACE-2 trial [see Clinical Studies] is indicated for use as an anticoagulant in patients undergoing percutaneous coronary intervention (PCI). Bivalirudin for Injection is indicated for patients with, or at risk of, heparin induced thrombocytopenia (HIT) or heparin induced thrombocytopenia and thrombosis syndrome (HITTS) undergoing PCI. Use With Aspirin Bivalirudin for Injection in these indications is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin [see DOSAGE AND ADMINISTRATION and Clinical Studies]. Limitation Of Use The safety and effectiveness of Bivalirudin for Injection have not been established in patients with acute coronary syndromes who are not undergoing PTCA or PCI. DOSAGE AND ADMINISTRATION Recommended Dose Bivalirudin for Injection is for intravenous administration only. Bivalirudin for Injection is intended for use with aspirin (300 to 325 mg daily) and has been studied only in patients receiving concomitant aspirin. For Patients Who Do Not Have HIT/HITTS The recommended dose of Bivalirudin for Injection is an intravenous (IV) bolus dose of 0.75 mg/kg, followed immediately by an infusion of 1.75 mg/kg/h for the duration of the PCI/PTCA procedure. Five min after the bolus dose has been administered, an activated clotting time (ACT) should be performed and an additional bolus of 0.3 mg/kg should be given if needed. GPI administration should be considered in the event that any of the conditions listed in the REPLACE-2 clinical trial description [see Clinical Studies] is present. For Patients Who Have HIT/HITTS The recommended dose of Bivalirudin for Injection in patients with HIT/HITTS undergoing PCI is an IV bolus of 0.75 mg/kg. This should be followed by a continuous infusion at a rate of 1.75 mg/kg/h for the duration of the procedure. For Ongoing Treatment Post-Procedure Bivalirudin for Injection infusion may be continued following PCI/PTCA for up to 4 hours postprocedure at the discretion of the treating physician. In patients with ST segment elevation myocardial infarction (STEMI) continuation of the Bivalirudin for Injection infusion at a rate of 1.75 mg/kg/h following PCI/PTCA for up to 4 hours post-procedure should be considered to mitigate risk of stent thrombosis. [see WARNINGS AND PRECAUTIONS]. After four hours, an additional IV infusion of Bivalirudin for Injection may be initiated at a rate of 0.2 mg/kg/h (low-rate infusion), for up to 20 hours, if needed. Dosing In Renal Impairment No reduction in the bolus dose is needed for any degree of renal impairment. The infusion dose of Bivalirudin for Injection may need to be reduced, and anticoagulant status monitored in patients with renal impairment. Patients with moderate renal impairment (30 to 59 mL/min) should receive an infusion of 1.75 mg/kg/h. If the creatinine clearance is less than 30 mL/min, reduction of the infusion rate to 1 mg/kg/h should be considered. If a patient is on hemodialysis, the infusion rate should be reduced to 0.25 mg/kg/h [see Use In Specific Populations]. Instructions For Administration Bivalirudin for Injection is intended for intravenous bolus injection and continuous infusion after reconstitution and dilution. To each 250 mg vial, add 5 mL of Sterile Water for Injection, USP. Gently swirl until all material is dissolved. Next, withdraw and discard 5 mL from a 50 mL infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection. Then add the contents of the reconstituted vial to the infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection to yield a final concentration of 5 mg/mL (e.g., 1 vial in 50 mL; 2 vials in 100 mL; 5 vials in 250 mL). The dose to be administered is adjusted according to the patient’s weight (see Table 1). If the low-rate infusion is used after the initial infusion, a lower concentration bag should be prepared. In order to prepare this lower concentration, reconstitute the 250 mg vial with 5 mL of Sterile Water for Injection, USP. Gently swirl until all material is dissolved. Next, withdraw and discard 5 mL from a 500 mL infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection. Then add the contents of the reconstituted vial to the infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection to yield a final concentration of 0.5 mg/mL. The infusion rate to be administered should be selected from the right-hand column in Table 1. Table 1: Dosing Table Using 5 mg/mL Concentration Using 0.5 mg/mL Concentration Weight (kg) Bolus 0.75 mg/kg (mL) Infusion 1.75 mg/kg/h (mL/h) Subsequent Low-rate Infusion 0.2 mg/kg/h (mL/h) 43 to 47 7 16 18 48 to 52 7.5 17.5 20 53 to 57 8 19 22 58 to 62 9 21 24 63 to 67 10 23 26 68 to 72 10.5 24.5 28 73 to 77 11 26 30 78 to 82 12 28 32 83 to 87 13 30 34 88 to 92 13.5 31.5 36 93 to 97 14 33 38 98 to 102 15 35 40 103 to 107 16 37 42 108 to 112 16.5 38.5 44 113 to 117 17 40 46 118 to 122 18 42 48 123 to 127 19 44 50 128 to 132 19.5 45.5 52 133 to 137 20 47 54 138 to 142 21 49 56 143 to 147 22 51 58 148 to 152 22.5 52.5 60 Bivalirudin for Injection should be administered via an intravenous line. No incompatibilities have been observed with glass bottles or polyvinyl chloride bags and administration sets. The following drugs should not be administered in the same intravenous line with Bivalirudin for Injection, since they resulted in haze formation, microparticulate formation, or gross precipitation when mixed with Bivalirudin for Injection: alteplase, amiodarone HCl, amphotericin B, chlorpromazine HCl, diazepam, prochlorperazine edisylate, reteplase, streptokinase, and vancomycin HCl. Dobutamine was compatible at concentrations up to 4 mg/mL but incompatible at a concentration of 12.5 mg/mL. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration. Preparations of Bivalirudin for Injection containing particulate matter should not be used. Reconstituted material will be a clear to slightly opalescent, colorless to slightly yellow solution. Storage After Reconstitution Do not freeze reconstituted or diluted Bivalirudin for Injection. Reconstituted material may be stored at 2 to 8°C for up to 24 hours. Diluted Bivalirudin for Injection with a concentration of between 0.5 mg/mL and 5 mg/mL is stable at room temperature for up to 24 hours. Discard any unused portion of reconstituted solution remaining in the vial. HOW SUPPLIED Dosage Forms And Strengths For injection: 250 mg of bivalirudin in a single-dose vial for reconstitution. Each vial contains 250 mg of bivalirudin equivalent to an average of 270 mg bivalirudin trifluoroacetate*. Following reconstitution with Sterile Water for Injection, the product is a clear to opalescent, colorless to slightly yellow solution, pH 5 to 6. *The range of bivalirudin trifluoroacetate is 260 to 280 mg based on a range of trifluoroacetic acid composition of 1.0 to 2.2 equivalents. Storage And Handling Bivalirudin for Injection is supplied as a sterile, lyophilized powder in single-dose, glass vials. Each vial contains 250 mg of bivalirudin equivalent to an average of 270 mg of bivalirudin trifluoroacetate*. *The range of bivalirudin trifluoroacetate is 260 to 280 mg based on a range of trifluoroacetic acid composition of 1.0 to 2.2 equivalents. Product No. NDC No. Strength 506210 63323-562-10 250 mg per vial 250 mg single-dose vial, packaged in tens. Store Bivalirudin for Injection dosage units at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. The container closure is not made with natural rubber latex. Distributed by: Fresenius Kabi, Fresenius Kabi USA, LLC Lake Zurich, IL 60047. Revised: June 2016.

INDICATIONS Percutaneous Transluminal Coronary Angioplasty (PTCA) Angiomax® (bivalirudin) is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA). Percutaneous Coronary Intervention (PCI) Angiomax with provisional use of glycoprotein IIb/IIIa inhibitor (GPI) as listed in the REPLACE-2 trial [see Clinical Studies] is indicated for use as an anticoagulant in patients undergoing percutaneous coronary intervention (PCI). Angiomax is indicated for patients with, or at risk of, heparin induced thrombocytopenia (HIT) or heparin induced thrombocytopenia and thrombosis syndrome (HITTS) undergoing PCI. Use With Aspirin Angiomax in these indications is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin [see DOSAGE AND ADMINISTRATION and Clinical Studies]. Limitation Of Use The safety and effectiveness of Angiomax have not been established in patients with acute coronary syndromes who are not undergoing PTCA or PCI. DOSAGE AND ADMINISTRATION Recommended Dose Angiomax is for intravenous administration only. Angiomax is intended for use with aspirin (300-325 mg daily) and has been studied only in patients receiving concomitant aspirin. For Patients Who Do Not Have HIT/HITTS The recommended dose of Angiomax is an intravenous (IV) bolus dose of 0.75 mg/kg, followed immediately by an infusion of 1.75 mg/kg/h for the duration of the PCI/PTCA procedure. Five min after the bolus dose has been administered, an activated clotting time (ACT) should be performed and an additional bolus of 0.3 mg/kg should be given if needed. GPI administration should be considered in the event that any of the conditions listed in the REPLACE-2 clinical trial description [see Clinical Studies] is present. For Patients Who Have HIT/HITTS The recommended dose of Angiomax in patients with HIT/HITTS undergoing PCI is an IV bolus of 0.75 mg/kg. This should be followed by a continuous infusion at a rate of 1.75 mg/kg/h for the duration of the procedure. For Ongoing Treatment Post Procedure Angiomax infusion may be continued following PCI/PTCA for up to 4 hours post-procedure at the discretion of the treating physician. In patients with ST segment elevation myocardial infarction (STEMI) continuation of the Angiomax infusion at a rate of 1.75 mg/kg/h following PCI/PTCA for up to 4 hours postprocedure should be considered to mitigate risk of stent thrombosis. [see WARNINGS AND PRECAUTIONS]. After four hours, an additional IV infusion of Angiomax may be initiated at a rate of 0.2 mg/kg/h (low-rate infusion), for up to 20 hours, if needed. Dosing In Renal Impairment No reduction in the bolus dose is needed for any degree of renal impairment. The infusion dose of Angiomax may need to be reduced, and anticoagulant status monitored in patients with renal impairment. Patients with moderate renal impairment (30-59 mL/min) should receive an infusion of 1.75 mg/kg/h. If the creatinine clearance is less than 30 mL/min, reduction of the infusion rate to 1 mg/kg/h should be considered. If a patient is on hemodialysis, the infusion rate should be reduced to 0.25 mg/kg/h [see Use In Specific Populations]. Instructions For Administration Angiomax is intended for intravenous bolus injection and continuous infusion after reconstitution and dilution. To each 250 mg vial, add 5 mL of Sterile Water for Injection, USP. Gently swirl until all material is dissolved. Next, withdraw and discard 5 mL from a 50 mL infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection. Then add the contents of the reconstituted vial to the infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection to yield a final concentration of 5 mg/mL (e.g., 1 vial in 50 mL; 2 vials in 100 mL; 5 vials in 250 mL). The dose to be administered is adjusted according to the patient's weight (see Table 1). If the low-rate infusion is used after the initial infusion, a lower concentration bag should be prepared. In order to prepare this lower concentration, reconstitute the 250 mg vial with 5 mL of Sterile Water for Injection, USP. Gently swirl until all material is dissolved. Next, withdraw and discard 5 mL from a 500 mL infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection. Then add the contents of the reconstituted vial to the infusion bag containing 5% Dextrose in Water or 0.9% Sodium Chloride for Injection to yield a final concentration of 0.5 mg/mL. The infusion rate to be administered should be selected from the right-hand column in Table 1. Table 1: Dosing Table Weight (kg) Using 5 mg/mL Concentration Using 0.5 mg/mL Concentration Bolus 0.75 mg/kg (mL) Infusion 1.75 mg/kg/h (mL/h) Subsequent Low-rate Infusion 0.2 mg/kg/h (mL/h) 43-47 7 16 18 48-52 7.5 17.5 20 53-57 8 19 22 58-62 9 21 24 63-67 10 23 26 68-72 10.5 24.5 28 73-77 11 26 30 78-82 12 28 32 83-87 13 30 34 88-92 13.5 31.5 36 93-97 14 33 38 98-102 15 35 40 103-107 16 37 42 108-112 16.5 38.5 44 113-117 17 40 46 118-122 18 42 48 123-127 19 44 50 128-132 19.5 45.5 52 133-137 20 47 54 138-142 21 49 56 143-147 22 51 58 148-152 22.5 52.5 60 Angiomax should be administered via an intravenous line. No incompatibilities have been observed with glass bottles or polyvinyl chloride bags and administration sets. The following drugs should not be administered in the same intravenous line with Angiomax, since they resulted in haze formation, microparticulate formation, or gross precipitation when mixed with Angiomax: alteplase, amiodarone HCl, amphotericin B, chlorpromazine HCl, diazepam, prochlorperazine edisylate, reteplase, streptokinase, and vancomycin HCl. Dobutamine was compatible at concentrations up to 4 mg/mL but incompatible at a concentration of 12.5 mg/mL. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration. Preparations of Angiomax containing particulate matter should not be used. Reconstituted material will be a clear to slightly opalescent, colorless to slightly yellow solution. Storage After Reconstitution Do not freeze reconstituted or diluted Angiomax. Reconstituted material may be stored at 2-8°C for up to 24 hours. Diluted Angiomax with a concentration of between 0.5 mg/mL and 5 mg/mL is stable at room temperature for up to 24 hours. Discard any unused portion of reconstituted solution remaining in the vial. HOW SUPPLIED Dosage Forms And Strengths For injection: 250 mg of bivalirudin in a single-dose vial for reconstitution. Each vial contains 250 mg of bivalirudin equivalent to an average of 275 mg bivalirudin trifluoroacetate*. Following reconstitution with Sterile Water for Injection, the product is a clear to opalescent, colorless to slightly yellow solution, pH 5-6. *The range of bivalirudin trifluoroacetate is 270 to 280 mg based on a range of trifluoroacetic acid composition of 1.7 to 2.6 equivalents. Storage And Handling Angiomax is supplied as a sterile, lyophilized powder in single-dose, glass vials. Each vial contains 250 mg of bivalirudin equivalent to an average of 275 mg of bivalirudin trifluoroacetate*. *The range of bivalirudin trifluoroacetate is 270 to 280 mg based on a range of trifluoroacetic acid composition of 1.7 to 2.6 equivalents. NDC 65293-001-01 Store Angiomax dosage units at 20 to 25°C (68 to 77°F). Excursions to 15 to 30°C permitted [see USP Controlled Room Temperature]. Marketed by: The Medicines Company, Parsippany, NJ 07054. Revised: Mar 2016

PATIENT INFORMATION Advise patients to watch carefully for any signs of bleeding or bruising and to report these to their health care provider when they occur. Advise patients to discuss with their health care provider their use of any other medications, including over-the-counter medications or herbal products, prior to bivalirudin use. Examples of other medications that should not be taken with bivalirudin are warfarin and heparin.

PATIENT INFORMATION Advise patients to watch carefully for any signs of bleeding or bruising and to report these to their health care provider when they occur. Advise patients to discuss with their health care provider their use of any other medications, including over-the-counter medications or herbal products, prior to Angiomax use. Examples of other medications that should not be taken with Angiomax are warfarin and heparin.

SIDE EFFECTS Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Bleeding In 6,010 patients undergoing PCI treated in the REPLACE-2 trial, bivalirudin patients exhibited statistically significantly lower rates of bleeding, transfusions, and thrombocytopenia as noted in Table 2. Table 2: Major Hematologic Outcomes REPLACE-2 (Safety Population) Bivalirudin with “provisional” GPI1 (n=2,914) Heparin + GPI (n=2,987) Protocol defined major hemorrhage2 (%) 2.3% 4.0% Protocol defined minor hemorrhage3 (%) 13.6% 25.8% TIMI defined bleeding4 - Major 0.6% 0.9% - Minor 1.3% 2.9% Non-access site bleeding - Retroperitoneal bleeding 0.2% 0.5% - Intracranial bleeding <0.1% 0.1% Access site bleeding - Sheath site bleeding 0.9% 2.4% Thrombocytopenia5 <100,000 0.7% 1.7% <50,000 0.3% 0.6% Transfusions - RBC 1.3% 1.9% - Platelets 0.3% 0.6% 1GPIs were administered to 7.2% of patients in the bivalirudin with provisional GPI group. 2Defined as the occurrence of any of the following: intracranial bleeding, retroperitoneal bleeding, a transfusion of ≥ 2 units of blood/blood products, a fall in hemoglobin > 4g/dL, whether or not bleeding site is identified, spontaneous or non-spontaneous blood loss with a decrease in hemoglobin >3g/dL. 3Defined as observed bleeding that does not meet the criteria for major hemorrhage. 4TIMI major bleeding is defined as intracranial, or a fall in adjusted Hgb >5g/dL or Hct of >15%: TIMI minor bleeding is defined as a fall in adjusted Hgb of 3 to <5 g/dL or a fall in adjusted Hct of 9 to <15%, with a bleeding site such as hematuria, hematemesis, hematomas, retroperitoneal bleeding or a decrease in Hgb of >4 g/dL with no bleeding site. 5If <100,000 and >25% reduction from baseline, or <50,000. In 4,312 patients undergoing PTCA for treatment of unstable angina in 2 randomized, double-blind studies comparing bivalirudin to heparin, bivalirudin patients exhibited lower rates of major bleeding and lower requirements for blood transfusions. The incidence of major bleeding is presented in Table 3. The incidence of major bleeding was lower in the bivalirudin group than in the heparin group. Table 3: Major Bleeding and Transfusions in BAT Trial (all patients )* Bivalirudin (n=2,161) Heparin (n=2,151) No. (%) Patients with Major hemorrhage1 79 (3.7) 199 (9.3) - with >3 g/dL fall in Hgb 41 (1.9) 124 (5.8) - with >5 g/dL fall in Hgb 14 (0.6) 47 (2.2) - retroperitoneal bleeding 5 (0.2) 15 (0.7) - intracranial bleeding 1 (<0.1) 2 (0.1) - required transfusions 43 (2.0) 123 (5.7) *No monitoring of ACT (or PTT) was done after a target ACT was achieved. 1Major hemorrhage was defined as the occurrence of any of the following, intracranial bleeding, retroperitoneal bleeding, clinically overt bleeding with a decrease in hemoglobin ≥ 3 g/dL or leading to a transfusion of > 2 units of blood. This table includes data from the entire hospitalization period. In the AT-BAT study, of the 51 patients with HIT/HITTS, 1 patient who did not undergo PCI had major bleeding during CABG on the day following angiography. Nine patients had minor bleeding (mostly due to access site bleeding), and 2 patients developed thrombocytopenia. Other Adverse Reactions Adverse reactions, other than bleeding, observed in clinical trials were similar between the bivalirudin treated patients and the control groups. Adverse reactions (related adverse events) seen in clinical studies in patients undergoing PCI and PTCA are shown in Tables 4 and 5. Table 4: Most Frequent (>0.2%) Treatment-related Adverse Events (reactions )(through 30 days ) in the REPLACE-2 Safety Population Bivalirudin with “provisional” GPI1 (n = 2,914) n (%) Heparin + GPI (n = 2,987) n (%) Patients with at least one treatment-related AE 78 (2.7) 115 (3.9) Thrombocytopenia 9 (0.3) 30 (1.0) Nausea 15 (0.5) 7 (0.2) Hypotension 7 (0.2) 11 (0.4) Angina pectoris 5 (0.2) 12 (0.4) Headache 6 (0.2) 5 (0.2) Injection site pain 3 (0.1) 8 (0.3) Nausea and vomiting 2 (0.1) 6 (0.2) Vomiting 3 (0.1) 5 (0.2) 1Note: A patient could have been more than one event in any category. Abbreviation: AE = Adverse Event. Table 5: Adverse Reactions Other Than Bleeding Occurring In ≥ 5% of Patients in Either Treatment Group in BAT Trial Event Treatment Groups Bivalirudin (n=2,161) Heparin (n=2,151) Number of Patients (%) Cardiovascular Hypotension 262 (12) 371 (17) Hypertension 135 (6) 115 (5) Bradycardia 118 (5) 164 (8) Gastrointestinal Nausea 318 (15) 347 (16) Vomiting 138 (6) 169 (8) Dyspepsia 100 (5) 111 (5) Genitourinary Urinary retention 89 (4) 98 (5) Miscellaneous Back pain 916 (42) 944 (44) Pain 330 (15) 358 (17) Headache 264 (12) 225 (10) Injection site pain 174 (8) 274 (13) Insomnia 142 (7) 139 (6) Pelvic pain 130 (6) 169 (8) Anxiety 127 (6) 140 (7) Abdominal pain 103 (5) 104 (5) Fever 103 (5) 108 (5) Nervousness 102 (5) 87 (4) Serious, non-bleeding adverse events were experienced in 2% of 2,161 bivalirudin-treated patients and 2% of 2,151 heparin-treated patients. The following individual serious non-bleeding adverse events were rare (>0.1% to <1%) and similar in incidence between bivalirudin- and heparin-treated patients. These events are listed by body system: Body as a Whole: fever, infection, sepsis; Cardiovascular: hypotension, syncope, vascular anomaly, ventricular fibrillation; Nervous: cerebral ischemia, confusion, facial paralysis; Respiratory: lung edema; Urogenital: kidney failure, oliguria. In the BAT trial, there was no causality assessment for adverse events. Immunogenicity/Re-Exposure In in vitro studies, bivalirudin exhibited no platelet aggregation response against sera from patients with a history of HIT/HITTS. Among 494 subjects who received bivalirudin in clinical trials and were tested for antibodies, 2 subjects had treatment-emergent positive bivalirudin antibody tests. Neither subject demonstrated clinical evidence of allergic or anaphylactic reactions and repeat testing was not performed. Nine additional patients who had initial positive tests were negative on repeat testing. Postmarketing Experience Because postmarketing adverse reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. The following adverse reactions have been identified during postapproval use of bivalirudin: fatal bleeding; hypersensitivity and allergic reactions including reports of anaphylaxis; lack of anticoagulant effect; thrombus formation during PCI with and without intracoronary brachytherapy, including reports of fatal outcomes; pulmonary hemorrhage; cardiac tamponade; and INR increased. DRUG INTERACTIONS In clinical trials in patients undergoing PCI/PTCA, co-administration of bivalirudin with heparin, warfarin, thrombolytics, or GPIs was associated with increased risks of major bleeding events compared to patients not receiving these concomitant medications. There is no experience with co-administration of bivalirudin and plasma expanders such as dextran.

SIDE EFFECTS Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Bleeding In 6010 patients undergoing PCI treated in the REPLACE-2 trial, Angiomax patients exhibited statistically significantly lower rates of bleeding, transfusions, and thrombocytopenia as noted in Table 2. Table 2: Major Hematologic Outcomes REPLACE-2 (Safety Population) ANGIOMAX with “provisional” GPI1 (n=2914) HEPARIN + GPI (n=2987) Protocol defined major hemorrhage2 (%) 2.3% 4.0% Protocol defined minor hemorrhage3 (%) 13.6% 25.8% TIMI defined bleeding4 - Major 0.6% 0.9% - Minor 1.3% 2.9% Non-access site bleeding - Retroperitoneal bleeding 0.2% 0.5% - Intracranial bleeding <0.1% 0.1% Access site bleeding - Sheath site bleeding 0.9% 2.4% Thrombocytopenia5 <100,000 0.7% 1.7% <50,000 0.3% 0.6% Transfusions - RBC 1.3% 1.9% - Platelets 0.3% 0.6% 1 GPIs were administered to 7.2% of patients in the Angiomax with provisional GPI group 2 Defined as the occurrence of any of the following: intracranial bleeding, retroperitoneal bleeding, a transfusion of ≥2 units of blood/blood products, a fall in hemoglobin > 4 g/dL, whether or not bleeding site is identified, spontaneous or non-spontaneous blood loss with a decrease in hemoglobin >3 g/Dl 3 Defined as observed bleeding that does not meet the criteria for major hemorrhage 4 TIMI major bleeding is defined as intracranial, or a fall in adjusted Hgb >5 g/dL or Hct of >15%: TIMI minor bleeding is defined as a fall in adjusted Hgb of 3 to <5 g/dL or a fall in adjusted Hct of 9 to <15%, with a bleeding site such as hematuria, hematemesis, hematomas, retroperitoneal bleeding or a decrease in Hgb of >4 g/dL with no bleeding site 5 If <100,000 and >25% reduction from baseline, or <50,000 In 4312 patients undergoing PTCA for treatment of unstable angina in 2 randomized, doubleblind studies comparing Angiomax to heparin, Angiomax patients exhibited lower rates of major bleeding and lower requirements for blood transfusions. The incidence of major bleeding is presented in Table 3. The incidence of major bleeding was lower in the Angiomax group than in the heparin group. Table 3: Major Bleeding and Transfusions in BAT Trial (all patients)* ANGIOMAX (n=2161) HEPARIN (n=2151) No. (%) Patients with Major hemorrhage1 79 (3.7) 199 (9.3) -with >3 g/dL fall in Hgb 41 (1.9) 124 (5.8) -with >5 g/dL fall in Hgb 14 (0.6) 47 (2.2) -retroperitoneal bleeding 5 (0.2) 15 (0.7) -intracranial bleeding 1 (<0.1) 2 (0.1) -Required transfusions 43 (2.0) 123 (5.7) * No monitoring of ACT (or PTT) was done after a target ACT was achieved. 1 Major hemorrhage was defined as the occurrence of any of the following, intracranial bleeding, retroperitoneal bleeding, clinically overt bleeding with a decrease in hemoglobin ≥3 g/dL or leading to a transfusion of ≥2 units of blood. This table includes data from the entire hospitalization period. In the AT-BAT study, of the 51 patients with HIT/HITTS, 1 patient who did not undergo PCI had major bleeding during CABG on the day following angiography. Nine patients had minor bleeding (mostly due to access site bleeding), and 2 patients developed thrombocytopenia. Other Adverse Reactions Adverse reactions, other than bleeding, observed in clinical trials were similar between the Angiomax treated patients and the control groups. Adverse reactions (related adverse events) seen in clinical studies in patients undergoing PCI and PTCA are shown in Tables 4 and 5. Table 4: Most Frequent (>0.2%) Treatment-related Adverse Events (reactions)(through 30 days) in the REPLACE-2 Safety Population ANGIOMAX with “provisional” GPI1 (n=2914) HEPARIN + GPI (n =2987) Patients with at least one treatment-related AE n (%) n (%) 78 (2.7) 115 (3.9) Thrombocytopenia 9 (0.3) 30 (1.0) Nausea 15 (0.5) 7 (0.2) Hypotension 7 (0.2) 11 (0.4) Angina pectoris 5 (0.2) 12 (0.4) Headache 6 (0.2) 5 (0.2) Injection site pain 3 (0.1) 8 (0.3) Nausea and vomiting 2 (0.1) 6 (0.2) Vomiting 3 (0.1) 5 (0.2) 1 Note: A patient could have been more than one event in any category. Abbreviation: AE = Adverse Event Table 5: Adverse Reactions Other Than Bleeding Occurring In ≥ 5% of Patients in Either Treatment Group in BAT Trial Event Treatment Groups ANGIOMAX (n=2161) HEPARIN (n=2151) Number of Patients (%) Cardiovascular Hypotension 262 (12) 371 (17) Hypertension 135 (6) 115 (5) Bradycardia 118 (5) 164 (8) Gastrointestinal Nausea 318 (15) 347 (16) Vomiting 138 (6) 169 (8) Dyspepsia 100 (5) 111 (5) Genitourinary Urinary retention 89 (4) 98 (5) Miscellaneous Back pain 916 (42) 944 (44) Pain 330 (15) 358(17) Headache 264 (12) 225 (10) Injection site pain 174 (8) 274 (13) Insomnia. 142 (7) 139 (6) Pelvic pain 130 (6) 169 (8) Anxiety 127 (6) 140 (7) Abdominal pain 103 (5) 104 (5) Fever 103 (5) 108 (5) Nervousness 102 (5) 87 (4) Serious, non-bleeding adverse events were experienced in 2% of 2161 Angiomax-treated patients and 2% of 2151 heparin-treated patients. The following individual serious non-bleeding adverse events were rare (>0.1% to <1%) and similar in incidence between Angiomax- and heparin-treated patients. These events are listed by body system: Body as a Whole: fever, infection, sepsis; Cardiovascular: hypotension, syncope, vascular anomaly, ventricular fibrillation; Nervous: cerebral ischemia, confusion, facial paralysis; Respiratory: lung edema; Urogenital: kidney failure, oliguria. In the BAT trial, there was no causality assessment for adverse events. Immunogenicity/Re-Exposure In in vitro studies, Angiomax exhibited no platelet aggregation response against sera from patients with a history of HIT/HITTS. Among 494 subjects who received Angiomax in clinical trials and were tested for antibodies, 2 subjects had treatment-emergent positive bivalirudin antibody tests. Neither subject demonstrated clinical evidence of allergic or anaphylactic reactions and repeat testing was not performed. Nine additional patients who had initial positive tests were negative on repeat testing. Postmarketing Experience Because postmarketing adverse reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. The following adverse reactions have been identified during postapproval use of Angiomax: fatal bleeding; hypersensitivity and allergic reactions including reports of anaphylaxis; lack of anticoagulant effect; thrombus formation during PCI with and without intracoronary brachytherapy, including reports of fatal outcomes; pulmonary hemorrhage; cardiac tamponade; and INR increased. DRUG INTERACTIONS In clinical trials in patients undergoing PCI/PTCA, co-administration of Angiomax with heparin, warfarin, thrombolytics, or GPIs was associated with increased risks of major bleeding events compared to patients not receiving these concomitant medications. There is no experience with co-administration of Angiomax and plasma expanders such as dextran.

WARNINGS Included as part of the "PRECAUTIONS" Section PRECAUTIONS Bleeding Events Although most bleeding associated with the use of bivalirudin in PCI/PTCA occurs at the site of arterial puncture, hemorrhage can occur at any site. An unexplained fall in blood pressure or hematocrit should lead to serious consideration of a hemorrhagic event and cessation of bivalirudin administration [see ADVERSE REACTIONS]. Bivalirudin should be used with caution in patients with disease states associated with an increased risk of bleeding. Acute Stent Thrombosis In Patients With STEMI Undergoing PCI Acute stent thrombosis (AST) (<4 hours) has been observed at a greater frequency in Bivalirudin for Injection treated patients (1.2%, 36/2,889) compared to heparin treated patients (0.2%, 6/2,911) with STEMI undergoing primary PCI. Among patients who experienced an AST, one fatality (0.03%) occurred in a bivalirudin treated patient and one fatality (0.03%) in a heparin treated patient. These patients have been managed by Target Vessel Revascularization (TVR). Patients should remain for at least 24 hours in a facility capable of managing ischemic complications and should be carefully monitored following primary PCI for signs and symptoms consistent with myocardial ischemia. Coronary Artery Brachytherapy An increased risk of thrombus formation, including fatal outcomes, has been associated with the use of Bivalirudin for Injection in gamma brachytherapy. If a decision is made to use Bivalirudin for Injection during brachytherapy procedures, maintain meticulous catheter technique, with frequent aspiration and flushing, paying special attention to minimizing conditions of stasis within the catheter or vessels [see ADVERSE REACTIONS]. Laboratory Test Interference Bivalirudin affects International Normalized Ratio (INR), therefore INR measurements made in patients who have been treated with Bivalirudin for Injection may not be useful for determining the appropriate dose of warfarin. Nonclinical Toxicology Carcinogenesis, Mutagenesis, Impairment Of Fertility No long-term studies in animals have been performed to evaluate the carcinogenic potential of bivalirudin. Bivalirudin displayed no genotoxic potential in the in vitro bacterial cell reverse mutation assay (Ames test), the in vitro Chinese hamster ovary cell forward gene mutation test (CHO/HGPRT), the in vitro human lymphocyte chromosomal aberration assay, the in vitro rat hepatocyte unscheduled DNA synthesis (UDS) assay, and the in vivo rat micronucleus assay. Fertility and general reproductive performance in rats were unaffected by subcutaneous doses of bivalirudin up to 150 mg/kg/day, about 1.6 times the dose on a body surface area basis (mg/m2) of a 50 kg person given the maximum recommended dose of 15 mg/kg/day. Use In Specific Populations Pregnancy Pregnancy Category B Reproductive studies have been performed in rats at subcutaneous doses up to 150 mg/kg/day, (1.6 times the maximum recommended human dose based on body surface area) and rabbits at subcutaneous doses up to 150 mg/kg/day (3.2 times the maximum recommended human dose based on body surface area). These studies revealed no evidence of impaired fertility or harm to the fetus attributable to bivalirudin. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. Bivalirudin is intended for use with aspirin [see INDICATIONS AND USAGE]. Because of possible adverse effects on the neonate and the potential for increased maternal bleeding, particularly during the third trimester, bivalirudin and aspirin should be used together during pregnancy only if clearly needed. Nursing Mothers It is not known whether bivalirudin is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when bivalirudin is administered to a nursing woman. Pediatric Use The safety and effectiveness of bivalirudin in pediatric patients have not been established. Geriatric Use In studies of patients undergoing PCI, 44% were ≥65 years of age and 12% of patients were ≥75 years old. Elderly patients experienced more bleeding events than younger patients. Patients treated with bivalirudin experienced fewer bleeding events in each age stratum, compared to heparin. Renal Impairment The disposition of bivalirudin was studied in PTCA patients with mild, moderate and severe renal impairment. The clearance of bivalirudin was reduced approximately 20% in patients with moderate and severe renal impairment and was reduced approximately 80% in dialysis-dependent patients [see CLINICAL PHARMACOLOGY]. The infusion dose of bivalirudin may need to be reduced, and anticoagulant status monitored in patients with renal impairment [see DOSAGE AND ADMINISTRATION].

WARNINGS Included as part of the PRECAUTIONS section. PRECAUTIONS Bleeding Events Although most bleeding associated with the use of Angiomax in PCI/PTCA occurs at the site of arterial puncture, hemorrhage can occur at any site. An unexplained fall in blood pressure or hematocrit should lead to serious consideration of a hemorrhagic event and cessation of Angiomax administration [see ADVERSE REACTIONS]. Angiomax should be used with caution in patients with disease states associated with an increased risk of bleeding. Acute Stent Thrombosis In Patients With STEMI Undergoing PCI Acute stent thrombosis (AST) (<4 hours) has been observed at a greater frequency in Angiomax treated patients (1.2%, 36/2889) compared to heparin treated patients (0.2%, 6/2911) with STEMI undergoing primary PCI. Among patients who experienced an AST, one fatality (0.03%) occurred in an Angiomax treated patient and one fatality (0.03%) in a heparin treated patient. These patients have been managed by Target Vessel Revascularization (TVR). Patients should remain for at least 24 hours in a facility capable of managing ischemic complications and should be carefully monitored following primary PCI for signs and symptoms consistent with myocardial ischemia. Coronary Artery Brachytherapy An increased risk of thrombus formation, including fatal outcomes, has been associated with the use of Angiomax in gamma brachytherapy. If a decision is made to use Angiomax during brachytherapy procedures, maintain meticulous catheter technique, with frequent aspiration and flushing, paying special attention to minimizing conditions of stasis within the catheter or vessels [see ADVERSE REACTIONS]. Laboratory Test Interference Angiomax affects International Normalized Ratio (INR), therefore INR measurements made in patients who have been treated with Angiomax may not be useful for determining the appropriate dose of warfarin. Nonclinical Toxicology Carcinogenesis, Mutagenesis, Impairment Of Fertility No long-term studies in animals have been performed to evaluate the carcinogenic potential of bivalirudin. Bivalirudin displayed no genotoxic potential in the in vitro bacterial cell reverse mutation assay (Ames test), the in vitro Chinese hamster ovary cell forward gene mutation test (CHO/HGPRT), the in vitro human lymphocyte chromosomal aberration assay, the in vitro rat hepatocyte unscheduled DNA synthesis (UDS) assay, and the in vivo rat micronucleus assay.  Fertility and general reproductive performance in rats were unaffected by subcutaneous doses of bivalirudin up to 150 mg/kg/day, about 1.6 times the dose on a body surface area basis (mg/m²) of a 50 kg person given the maximum recommended dose of 15 mg/kg/day. Use In Specific Populations Pregnancy Pregnancy Category B Reproductive studies have been performed in rats at subcutaneous doses up to 150 mg/kg/day, (1.6 times the maximum recommended human dose based on body surface area) and rabbits at subcutaneous doses up to 150 mg/kg/day (3.2 times the maximum recommended human dose based on body surface area). These studies revealed no evidence of impaired fertility or harm to the fetus attributable to bivalirudin. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. Angiomax is intended for use with aspirin [see INDICATIONS AND USAGE]. Because of possible adverse effects on the neonate and the potential for increased maternal bleeding, particularly during the third trimester, Angiomax and aspirin should be used together during pregnancy only if clearly needed. Nursing Mothers It is not known whether bivalirudin is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Angiomax is administered to a nursing woman. Pediatric Use The safety and effectiveness of Angiomax in pediatric patients have not been established. Geriatric Use In studies of patients undergoing PCI, 44% were ≥65 years of age and 12% of patients were ≥75 years old. Elderly patients experienced more bleeding events than younger patients. Patients treated with Angiomax experienced fewer bleeding events in each age stratum, compared to heparin. Renal Impairment The disposition of Angiomax was studied in PTCA patients with mild, moderate and severe renal impairment. The clearance of Angiomax was reduced approximately 20% in patients with moderate and severe renal impairment and was reduced approximately 80% in dialysisdependent patients [see CLINICAL PHARMACOLOGY]. The infusion dose of Angiomax may need to be reduced, and anticoagulant status monitored in patients with renal impairment [seeDOSAGE AND ADMINISTRATION].