(and www.circ.ahajournals.org r23-r35). A Phase 3 International, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Efficacy and Safety.

Slides:



Advertisements
Similar presentations
August 30, 2009 at CET. Ticagrelor compared with clopidogrel in patients with acute coronary syndromes – the PLATO trial.
Advertisements

TIMI 11BESSENCE Enoxaparin for UA/NQMI: TIMI 11B-ESSENCE Meta-Analysis Antman EM et al, Circulation 1999 Oct 12;100(15):
Standard Medical Therapy TRA 40 mg mg/d TRA 40 mg mg/d Placebo EP:CV Death/MI/stroke/hosp for RI/urgent coronary revasc. 1  EP:CV Death/MI/stroke/hosp.
PCI - A prospective, randomized, double- blind substudy of patients undergoing PCI in the CURE trial.
The FINESSE Trial: Results of the Formal Low Molecular Weight Heparin Substudy Facilitated INtervention with Enhanced Reperfusion Speed to Stop Events.
Keith A A Fox Royal Infirmary & University of Edinburgh CURE and PCI-CURE.
Update on the Medical Management of Acute Coronary Syndrome.
Long-term Outcomes of Patients with ACS and Chronic Renal Insufficiency Undergoing PCI and being treated with Bivalirudin vs UFH/Enoxaparin plus a GP IIb/IIIa.
A Risk Score for Predicting Coronary Artery Bypass Surgery in Patients with Non-ST Elevation Acute Coronary Syndromes Sai Sadanandan, MD*; Christopher.
Slide Source: Lipids Online Slide Library Pravastatin or Atorvastatin Evaluation and Infection Therapy (PROVE IT): Design Cannon CP.
“Adjunctive Therapy” Non ST segment elevation ACS Dr M R Thomas King’s College Hospital. Advanced Angioplasty 2002.
Management of Acute Myocardial Infarction Minimal Acceptable vs Optimal Care Hussien H. Rizk, MD Cairo University.
Stanford ACS Guidelines 2003 David P. Lee, M.D. John S. Schroeder, M.D. *Donald Schreiber, M.D. Division of Cardiovascular Medicine and *Department of.
TNT: Study Design Treating to New Targets 2 5 years 10,001 Patients Clinically evident CHD LDL-C 130  250 mg/dL following up to 8-week washout and 8-week.
lopidogrel in nstable Angina to Prevent ecurrent vents
TRial to Assess Improvement in Therapeutic Outcomes by Optimizing Platelet InhibitioN with Prasugrel TRITON-TIMI 38 TRITON-TIMI 38 Elliott M. Antman, MD.
Prasugrel Compared to Clopidogrel in Patients with Acute Coronary Syndromes Undergoing PCI with Stenting: the TRITON - TIMI 38 Stent Analysis Stephen D.
Clinical Trial Results. org Pexelizumab for Acute ST-Elevation Myocardial Infarction in Patients Undergoing Primary Percutaneous Coronary Intervention.
Clopidogrel in ACS: Overview Investigator, TIMI Study Group Associate Physician, Cardiovascular Division, BWH Assistant Professor of Medicine, Harvard.
Kenneth W. Mahaffey, Zhen Huang, Pierluigi Tricoci, Frans Van de Werf, Harvey D. White, Paul W. Armstrong, Claes Held, Sergio Leonardi, Philip E. Aylward,
VBWG CHARISMA Clopidogrel for High Atherothrombotic Risk and Ischemic Stabilization, Management, and Avoidance trial.
VBWG OASIS-5 The Fifth Organization to Assess Strategies in Acute Ischemic Syndromes trial.
ACTIVE Clopidogrel plus Aspirin versus Aspirin in Patients Unsuitable for Warfarin.
C.R.E.D.O. C lopidogrel for the R eduction of E vents D uring O bservation Multicenter Multinational (USA, Canada) Prospective Randomized Double Blind.
TIMI 11A A Multicenter Trial of the Safety and Tolerability of Two Doses of Enoxaparin in Patients With Unstable Angina and Non-Q-Wave Myocardial Infarction.
New Treatment Advances in Acute Coronary Syndrome.
Prasugrel vs. Clopidogrel for Acute Coronary Syndromes Patients Managed without Revascularization — the TRILOGY ACS trial On behalf of the TRILOGY ACS.
Background Fibrinolytic Rx in STEMI is limited by inadequate reperfusion and/or reocclusion in ~25% of pts. An occluded infarct-related artery is associated.
Aspirin Resistance: Significance, Detection and Clinical Management of This Real Phenomenon Webcast May 10 th, 2004 Sponsored by.
What’s New in Acute Coronary Syndromes? Claudia Bucci BScPhm, PharmD Clinical Coordinator, Cardiovascular Diseases Sunnybrook Health Sciences Centre 13.
Vorapaxar for Secondary Prevention in Patients with Prior Myocardial Infarction Benjamin M. Scirica, MD, MPH On behalf of the TRA 2°P-TIMI 50 Steering.
Safety and Efficacy of Intravenous Enoxaparin in Elective Percutaneous Coronary Intervention: An International Randomised Evaluation One year follow-up.
Naotsugu Oyama, MD, PhD, MBA A Trial of PLATelet inhibition and Patient Outcomes.
Do Tirofiban And ReoPro Give Similar Efficacy Outcomes Trial Presented at AHA Scientific Sessions Nov. 15, 2000.
1 HOT LINE PRESENTATION World Congress of Cardiology 2006 Barcelona, Spain September 5, 2006 Warfarin Antiplatelet Vascular Evaluation PAD Patients.
The Additive Value of Tirofiban Administered With the High-Dose Bolus in the Prevention of Ischemic Complications During High-Risk Coronary Angioplasty.
The INT egrelin and E noxaparin R andomized assessment of A cute C oronary syndrome Treatment T rial Sponsored by the Canadian Heart Research Centre, Key.
Clinical Trial Results. org Increased Risk in Patients with High Platelet Aggregation Receiving Chronic Clopidogrel Therapy Undergoing Percutaneous Coronary.
Xemilofiban 10 mg TID Xemilofiban 20 mg TID Placebo TID RandomizationRandomization Xemilofiban 20 mg Placebo PCI 30 to 90 min prior to PTCR Stented patients.
Acute Coronary Syndrome David Aymond, MD. ACS Definition: Myocardial ischemia typically due to atherosclerotic plaque rupture  Coronary thrombosis ACS.
THE MEDICINES COMPANY ® ® N = 9000 SA/NSTEMI/STEMI Maintenance Plavix PCI PLATFORM Screening Cangrelor infusion Placebo infusion PlavixPlacebo Plavix PCI.
TACTICS- TIMI 18 Treat Angina with Aggrastat TM and Determine Cost of Therapy with an Invasive or Conservative Strategy.
1 Advanced Angioplasty London, England 27 January, 2006 Jörg Michael Rustige,MD Medical Director Lilly Critical Care Europe, Geneva.
GUSTO IV ACS: Trial Design Abciximab versus placebo in very high-risk patients with non-ST elevation acute coronary syndromes: – ST  > 0.5 mm or – elevated.
NSTE Acute Coronary Syndromes
Hypothesis: baseline risk status of the patients and proximity to a recent cardiovascular event influence the response to dual anti-platelet therapy. Patients.
VBWG OASIS-6 The Sixth Organization to Assess Strategies in Acute Ischemic Syndromes trial.
Bivalirudin: Myths vs Reality? Dr Reman McDonagh Nycomed UK Ltd Conflict of Interest: Senior Manager working for Nycomed UK Ltd.
Gregg W. Stone MD for the ACUITY Investigators Gregg W. Stone MD for the ACUITY Investigators A Prospective, Randomized Trial of Bivalirudin in Acute Coronary.
Gender Differences in Long-Term Outcomes Following PCI of Patients with Non-ST Elevation ACS: Results from the ACUITY Trial Alexandra J. Lansky on behalf.
WarfarinApixaban Primary outcome: major/clinically relevant bleeding (through 6 months) Secondary objective: Death, MI, stroke, stent thrombosis Randomize.
Gregg W. Stone MD for the ACUITY Investigators A Prospective, Randomized Trial of Bivalirudin in Acute Coronary Syndromes Final One-Year Results from the.
Duration Safety and Efficacy of Bivalirudin in patients undergoing PCI: The impact of duration of infusion in ACUITY trial Dr. David Cox Lehigh Valley.
Double-blind, randomized trial in 4,162 patients with Acute Coronary Syndrome
The Opus Trial. Antithrombotic Therapy Stable Angina Unstable Angina ST Elevation MI Non-Q wave MI Thrombolysis Non-ST Elevation MI Q wave MI.
Bivalirudin Monotherapy Improves 30-day Clinical Outcomes in Diabetics with Acute Coronary Syndrome: Report from the ACUITY Trial Frederick Feit, Steven.
Learning from the Recently Completed Oral Glycoprotein IIb/IIIa Receptor Antagonist Trials Christopher Cannon, M.D. Brigham and Women’s Hospital Boston,
Clinical Trial Commentary
MCV Campus Ginger Edwards.
SPIRE Program: Studies of PCSK9 Inhibition and the Reduction of Vascular Events Unanticipated attenuation of LDL-c lowering response to humanized PCSK9.
Oral Anticoagulation and Preventing Stent Thrombosis
Disclosures. Evaluating Recent Clinical Trial Data in the Secondary Prevention of ACS.
TIMI IIIA Protocol Design 391 Patients with Unstable Angina / NQWMI
August 30, 2009 at CET. Ticagrelor compared with clopidogrel in patients with acute coronary syndromes – the PLATO trial.
Erasmus MC, Thoraxcenter
What oral antiplatelet therapy would you choose?
Clinical Trial Commentary
OASIS-5: Study Design Randomize N=20,078 Enoxaparin (N=10,021)
SPIRE Program: Studies of PCSK9 Inhibition and the Reduction of Vascular Events Unanticipated attenuation of LDL-c lowering response to humanized PCSK9.
Presenter Disclosure Information
Presentation transcript:

(and r23-r35). A Phase 3 International, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Efficacy and Safety Of Orbofiban in Patients with Unstable Coronary Syndromes Cannon CP et al. Circulation 2000;102:

Need for Long-Term Antiplatelet Therapy lMarkers of platelet activation persist 1 month post ACS -Ault K, et al. P selectin in TIMI 12 trial. JACC 1999;33: lAngioscopy: Thrombus persists 1 month post ACS -Van Belle, et al. Circulation 1998;97:26-33 lEvents persist beyond acute period: In the TIMI 3 Registry, Death/MI/Rec Ischemia -In-hospital = 10.5% -One year = 28.3% lBenefit of IIb/IIIa inhibition achieved only during IV infusion period (PURSUIT, PRISM-PLUS)

U.S. 2704Belgium232 Switzerl.65 Canada2064Germany 224 Mexico60 Israel784Poland218 Italy52 Netherl.674U.K.202 Denmark32 Spain568 Australia168 Norway22 Czech R.532 France163 Austria21 Argentina316 Chile145 Finland19 Brazil277S Africa130 N Zealand16 Russia266 Ireland99 Portugal14 Hungary235 Patients Randomized = 10,288 Cannon CP et al. Circulation 2000;102:

TIMI Study Chairman’s Office Eugene Braunwald, MD Christopher Cannon, MD Christopher Cannon, MD Carolyn McCabe, BS Carolyn McCabe, BS Nottingham Clinical Trial Allan Skene, PhD Data Centre Robert Wilcox, MD Andrew Foxley Andrew Foxley Andrew Charlesworth Andrew Charlesworth Sponsor - G.D. Searle: John Alexander, MD Robert Anders, PharmD Robert Anders, PharmD Daniel Burns Daniel Burns Central Units Cannon CP et al. Circulation 2000;102:

Eligibility Criteria n Inclusion Criteria: n Rest ischemic pain > 5 mins within 72 hrs with any 1: u ECG changes, Positive enzymes, (Hx coronary, peripheral or cerebrovasc disease, diabetes) u Major Exclusion Criteria: u Age < 18 years u Renal insufficiency (creatinine >1.6 mg/dl or a estimated creatinine clearance of 1.6 mg/dl or a estimated creatinine clearance of <40 cc/min) u Increased bleeding risk (Hx. Plts, GI bleed) u Need for warfarin, chronic NSAIDs u ReoPro/IIb/IIIa inhibitor Rx for index event

Study Design ASA mg daily Orbofiban 50 mg BID Orbo 50 mg BID x 30 days then Orbo 30 mg BID Placebo BID Other Meds, Cath/Revasc per MD F/U Day 14, Day 30 Follow-up visit every 3 months Primary endpoint to 30 days + follow-up Death, MI Urgent Revasc, Ischemia -> Rehosp, or Stroke Randomize 1:1:1 Patient with Unstable Coronary Syndrome <72 hours 30 days: orbofiban vs. placebo p=0.01 F/U: each dose vs. placebo p=0.02 N=10,288

Baseline Characteristics

Day 30 Outcomes Plac.Orbo 50/30 Orbo 50/50 Orbo (All) P value Death MI Urg Rev < Isch-rehosp ICH Non-ICH Composite Death /MI Cannon CP et al. Circulation 2000;102:

10 Month Outcomes Cannon CP et al. Circulation 2000;102:

TIMI Classification - Underlying Event Leading to Death No. Deaths Progressive Sudden Non-Ischemic Bleeding New Thrombotic Event Unclassified Orbo 50/50PlaceboOrbo 50/30 * * *p=0.03 Cannon CP et al. Circulation 2000;102:

Bleeding - Day 30 Cannon CP et al. Circulation 2000;102:

Bleeding - 10 Months Cannon CP et al. Circulation 2000;102:

Thrombocytopenia by Study Drug 30 Day 50-80,000 (%) 20-50,000 (%) <20,000 (%) 10 Months 50-80,000 (%) 20-50,000 (%) <20,000 (%) Placebo Orbo 50/ Orbo 50/ P value / NS / / / NS / / 0.01 Cannon CP et al. Circulation 2000;102:

Day 2 Results Cannon CP et al. Circulation 2000;102:

Day 2 Results Cannon CP et al. Circulation 2000;102:

Plac Orbo Int. P Age< 65 Age > 65 Men Women No prior CHF Prior CHF Acute MI UA Killiip I Killip II-IV Relative Risk Subgroups: 30 Day Mortality Orbo better Orbo Worse Circulation 2000;102:

Subgroups: 30 Day Mortality Day Mortality Plac Orbo Int P. CC > 100 CC < 100 No Heparin Heparin PCI pre-R No PCI PCI pre/post No PCI OrboBetter Orbo Worse Relative Risk Cannon CP et al. Circulation 2000;102:

Subgroups: 10 Month Composite Plac Orbo Int. P Age< 65 Age > 65 Men Women No prior CHF Prior CHF Acute MI UA Killiip I Killip II-IV Relative Risk Orbo better Orbo Worse Cannon CP et al. Circulation 2000;102:

CC > 100 CC < 100 No Heparin Heparin PCI pre-R No PCI PCI pre/post No PCI Orbo Better Orbo Worse Plac Orbo Int. P Relative Risk Subgroups: 10 Month Composite Cannon CP et al. Circulation 2000;102:

Summary l Orbofiban: l Minimal efficacy benefit overall in ACS l Greater benefit in PCI l Substudies:  P-selectin, FGN binding l  mortality, l Small absolute % l  thrombotic events l -> ? Prothrombotic, ?Unstable patients l Major bleeding, thrombocytopenia higher, but in acceptable range Cannon CP et al. Circulation 2000;102:

Potential Explanations - Future Directions l PK/PD variability, peak trough - è Longer T1/2, ? Adjust with platelet monitoring l Only modest benefit in non-PCI ACS patients l Recurrent events not platelet -mediated?- unlikely l Concomitant Rx beyond ASA? è ? Clopidogrel to  Platelet Activation, è ? Antithrombin to inhibit clotting cascade l ? Prothrombotic effects: è Need drugs with tight binding Cannon CP et al. Circulation 2000;102: