Potential Utility of rNAPC2 in ACS: Potential Utility of rNAPC2 in ACS: Phase 2 Heparin Replacement Trial Phase 2 Heparin Replacement Trial Evaluating RNAPc2 In Acute Coronary Evaluating RNAPc2 In Acute Coronary Syndromes Syndromes Robert P. Giugliano, MD, SM, Associate Physician, Cardiovascular Division Brigham and Women's Hospital Assistant Professor in Medicine Harvard Medical School Boston, MA
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Potential Utility of rNAPC2 in ACS: Phase 2 Heparin Replacement Trial Evaluating RNAPc2 In Acute Coronary Syndromes Potential Utility of rNAPC2 in ACS:
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Potential Utility of rNAPC2 in ACS: Potential Utility of rNAPC2 in ACS: Phase 2 Heparin Replacement Trial Phase 2 Heparin Replacement Trial
Evaluating RNAPc2 In Acute Coronary Evaluating RNAPc2 In Acute Coronary SyndromesSyndromes
Robert P. Giugliano, MD, SM, Associate Physician, Cardiovascular Division
Brigham and Women's HospitalAssistant Professor in Medicine
Harvard Medical SchoolBoston, MA
Novel Tissue Factor / Factor VIIa Inhibitor Reduces Ischemia in Patients with NSTE-ACS: Results of the Dose-Ranging and Heparin De-Escalation Phases of the ANTHEM-TIMI 32 Trial
RP Giugliano1, SD Wiviott1, DI Simon2, MJ Schweiger3, MA Leesar4, PH Stone1, R Bach5, A Skene6, SR Deitcher7, E Braunwald1
on behalf of the ANTHEM-TIMI 32 Investigators
(1) Brigham & Women’s Hospital, Boston, MA. (2) University Hospitals – Case Medical Center, Cleveland, OH. (3) Baystate Medical Center, Springfield, MA. (4)U of Louisville,
Louisville, KY. (5) Washington U School of Medicine, St. Louis, MO. (6) Nottingham Clinical Research Limited, Nottingham, UK. (7) Nuvelo, Inc., San Carlos, USA
DisclosuresDisclosures
Accumetrics, Inc. Amgen, Inc. AstraZeneca PharmaceuticalsBaxterBayer Healthcare LLCBeckman Coulter, Inc. Biosite IncorporatedBristol-Myers SquibbCardioKinetixCV Therapeutics, Inc. Eli Lilly and CompanyFoldRxGlaxoSmithKlineINO Therapeutics LLCInotek Pharmaceuticals Corp
Accumetrics, Inc. Amgen, Inc. AstraZeneca PharmaceuticalsBaxterBayer Healthcare LLCBeckman Coulter, Inc. Biosite IncorporatedBristol-Myers SquibbCardioKinetixCV Therapeutics, Inc. Eli Lilly and CompanyFoldRxGlaxoSmithKlineINO Therapeutics LLCInotek Pharmaceuticals Corp
Integrated Therapeutics CorpKAI PharmaceuticalsMerck & Co., Inc.Millennium Pharmaceuticals, Inc. Novartis PharmaceuticalsNuvelo, Inc. Ortho-Clinical Diagnostics, Inc. Pfizer, Inc. Roche Diagnostics CorporationRoche Diagnostics GmbHSanofi-AventisSanofi-Synthelabo RechercheSchering-PloughSt Jude MedicalThe National Institutes of Health
Integrated Therapeutics CorpKAI PharmaceuticalsMerck & Co., Inc.Millennium Pharmaceuticals, Inc. Novartis PharmaceuticalsNuvelo, Inc. Ortho-Clinical Diagnostics, Inc. Pfizer, Inc. Roche Diagnostics CorporationRoche Diagnostics GmbHSanofi-AventisSanofi-Synthelabo RechercheSchering-PloughSt Jude MedicalThe National Institutes of Health
The TIMI Study Group received research/grant support in the last 2 yrs through Brigham & Women’s Hospital from (alphabetical order):
The TIMI Study Group received research/grant support in the last 2 yrs through Brigham & Women’s Hospital from (alphabetical order):
MJ Schweiger, MA Leesar, R Bach, and A Skene received research grant support from Nuvelo; SR Deitcher is an employee of Nuvelo
MJ Schweiger, MA Leesar, R Bach, and A Skene received research grant support from Nuvelo; SR Deitcher is an employee of Nuvelo
Background Exposure of tissue factor (TF) initiates coagulation at
sites of vascular injury (plaque rupture, PCI) rNAPc2 is a recombinant, modified version of NAPc2
(derived from the hookworm) that provides potent factor X(a)-dependent inhibition of the TF/fVIIa complex
rNAPc2 prevented new thrombin generation in a dose-dependent manner in phase 2 studies of elective knee surgery and elective PTCA
Ischemia during continuous ECG monitoring identifies patients with ACS at high risk of adverse cardiac events
Enoxaparin was associated with less ischemia based on continuous ECG and better clinical outcomes than UFH, suggesting more proximal inhibition may be more effective than distal inhibition of the coagulation cascade
Trial Design: Dose RangingnSTE ACS -> Early Catheterization
ASA, Enox or UFH, GP IIb/IIIa*, clopidogrel*ASA, Enox or UFH, GP IIb/IIIa*, clopidogrel*
PK, PD: pre-dose, 2-6h, 48h, d7, d42Continuous ECG x 7 daysClinical f/u to 6 months
Major Endpoints
Safety
Major/Minor Bleed
Efficacy
F1+2, PT, PK
Holter Ischemia* Encouraged per current practice guidelines† 10 mcg/kg dose panel repeated
Blinded Randomized 4:1
nSTE ACS
Early Cath
nSTE ACS
Early Cath
Heparin De-Escalation (HDE) Design (n=52)
ASA
GP IIb/IIIa*
clopidogrel*
ASA
GP IIb/IIIa*
clopidogrel*
* Encouraged per current practice guidelines† 30 U/kg bolus (max 2500 U); 6 U/kg/h (max 600 U/h)‡ Defined as use of open-label anticoagulant to manage a thrombotic complication
rNAPc2
10 mcg/kg
rNAPc2
10 mcg/kg
½ Std† UFH (n=26)½ Std† UFH (n=26)
No UFH (n=26)No UFH (n=26)
2 Sequential Panels
Unblinded
PK, PD, Cont ECG, 6 mth clinicalAngiograms reviewed by Core LabThrombosis monitored by Investigators
Endpoints
Major/Minor Bleed
Thrombotic Bailout‡
F1+2, PT, PK
Holter Ischemia
1
2
Entry Criteria and Study Schema
rNAPc2/placebo
(rNAPc2/placebo)
Angio +/- PCIAngio +/- PCI
IV GP IIb/IIIa (encouraged)
144h144h00 48h48h 96h96h
R in hospital
192h192h(8d)(8d)
Enox q 12h or UFHAspirin 75-325 mg daily x 6 mths
Inclusion: Age 18-75, rest sx > 5min w/i 48h c/w ACS+ markers or ST deviation or TIMI Risk Score > 3Planned early invasive strategy
*p < 0.05 vs placebo † p = 0.12 vs placebo ‡ p = 0.051 vs ½ Std heparin.
Note: TBO was prospectively assessed only during heparin de-escalation, 1 case was retrospectively identified in patients receiving 10 mcg/kg rNAPc2 + standard heparin
Clinical Endpoints at 42 DaysrNAPc2 placebo (n=215) (n = 40)
All-cause Mortality 0 0New Myocardial Infarct* 2 3Clinical Rec Ischemia* 8 8D / MI* / RI* 10 10 Holter ischemia* 0-7 days 18 21Revasc post discharge 10 13Stroke 0.5 0Any of the above 30 38
Data shown are % of patients* Central blinded adjudicated All p = NS
rNAPc2 did not increase bleeding despite dose-related increase in INR
Higher dose rNAPc2 (> 7.5 mcg/kg) suppressed new thrombin generation and these doses ischemia by 50%
Some heparin may be necessary to avoid procedure-related thrombosis
These proof of concept data warrant larger-scale evaluation to determine if rNAPc2 improves clinical outcomes