TY - JOUR
T1 - Recombinant nematode anticoagulant protein c2, an inhibitor of the tissue factor/factor VIIa complex, in patients undergoing elective coronary angioplasty
AU - Moons, Arno H. M.
AU - Peters, Ron J. G.
AU - Bijsterveld, Nick R.
AU - Piek, Jan J.
AU - Prins, Martin H.
AU - Vlasuk, George P.
AU - Rote, William E.
AU - Büller, Harry R.
PY - 2003
Y1 - 2003
N2 - OBJECTIVES We investigated the safety and pharmacodynamics of escalating doses of recombinant nematode anticoagulant protein c2 (rNAPc2) in patients undergoing elective coronary angioplasty. BACKGROUND Recombinant NAPc2 is a potent inhibitor of the tissue factor/factor VIIa complex, which has the potential to reduce the risk of thrombotic complications in coronary artery disease. METHODS In a randomized, double-blinded, dose-escalation, multicenter trial, 154 patients received placebo or rNAPc2 at doses of 3.5, 5.0, 7.5, and 10.0 mug/kg body weight as a single subcutaneous administration 2 to 6 h before angioplasty. All patients received aspirin, unfractionated heparin during angioplasty, and clopidogrel in case of stent implantation. RESULTS Minor bleeding rates for the doses 3.5 to 7.5 mug/kg were comparable to that with placebo (6.7%), whereas an incidence of 26.9% was observed at the 10.0-mug/kg dose level (p <0.01). Major bleedings occurred in the 5.0-mug/kg (n = 3) and 7.5-mug/kg (n = 1) dose groups. The three patients in the 5.0-mug/kg dose group also received a glycoprotein IIb/IIIa receptor inhibitor at the moment of major bleeding. Systemic thrombin generation, as measured by prothrombin fragment 1+2 (F1+2), was suppressed in all rNAPc2 dose groups to levels below pretreatment values for at least 36 h. In the placebo group, a distinct increase of F1+2 levels was observed following cessation of heparin. CONCLUSIONS Inhibition of the tissue factor/factor VIIa complex with rNAPc2, at doses up to 7.5 mug/kg, in combination with aspirin, clopidogrel, and unfractionated heparin appears to be a safe and effective strategy to prevent thrombin generation during coronary angioplasty. (J Am Coll Cardiol 2003;41:2147-53) (C) 2003 by the American College of Cardiology Foundation
AB - OBJECTIVES We investigated the safety and pharmacodynamics of escalating doses of recombinant nematode anticoagulant protein c2 (rNAPc2) in patients undergoing elective coronary angioplasty. BACKGROUND Recombinant NAPc2 is a potent inhibitor of the tissue factor/factor VIIa complex, which has the potential to reduce the risk of thrombotic complications in coronary artery disease. METHODS In a randomized, double-blinded, dose-escalation, multicenter trial, 154 patients received placebo or rNAPc2 at doses of 3.5, 5.0, 7.5, and 10.0 mug/kg body weight as a single subcutaneous administration 2 to 6 h before angioplasty. All patients received aspirin, unfractionated heparin during angioplasty, and clopidogrel in case of stent implantation. RESULTS Minor bleeding rates for the doses 3.5 to 7.5 mug/kg were comparable to that with placebo (6.7%), whereas an incidence of 26.9% was observed at the 10.0-mug/kg dose level (p <0.01). Major bleedings occurred in the 5.0-mug/kg (n = 3) and 7.5-mug/kg (n = 1) dose groups. The three patients in the 5.0-mug/kg dose group also received a glycoprotein IIb/IIIa receptor inhibitor at the moment of major bleeding. Systemic thrombin generation, as measured by prothrombin fragment 1+2 (F1+2), was suppressed in all rNAPc2 dose groups to levels below pretreatment values for at least 36 h. In the placebo group, a distinct increase of F1+2 levels was observed following cessation of heparin. CONCLUSIONS Inhibition of the tissue factor/factor VIIa complex with rNAPc2, at doses up to 7.5 mug/kg, in combination with aspirin, clopidogrel, and unfractionated heparin appears to be a safe and effective strategy to prevent thrombin generation during coronary angioplasty. (J Am Coll Cardiol 2003;41:2147-53) (C) 2003 by the American College of Cardiology Foundation
U2 - https://doi.org/10.1016/S0735-1097(03)00478-9
DO - https://doi.org/10.1016/S0735-1097(03)00478-9
M3 - Article
C2 - 12821239
SN - 0735-1097
VL - 41
SP - 2147
EP - 2153
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 12
ER -