Author(s): Markus HS, McCollum C, Imray C, Goulder MA, Gilbert J, et al.
Background and purpose:Inhibition of von Willebrand factor offers a novel approach to prevention of stroke and myocardial ischemia but has not yet been demonstrated to show efficacy on clinically relevant end points. ARC1779 is an aptamer that inhibits the prothrombotic function of von Willebrand factor by binding to the A1 domain of von Willebrand factor and thereby blocking its interaction with glycoprotein. Phase 1 studies suggest it inhibits platelet aggregation with less increase in bleeding than conventional antiplatelet agents. The effect of ARC 1779 on cerebral emboli immediately after carotid endarterectomy was investigated in a randomized clinical trial.
Methods:Patients undergoing carotid endarterectomy were randomized double-blind to ARC1779 or placebo administered intravenously. Transcranial Doppler recording, to detect cerebral embolic signals, was performed in the first 3 hours postoperatively. The primary end point was time to first embolic signals.
Results:Thirty-six patients were recruited, 18 in each arm. The Kaplan-Meier median time to first embolic signals was 83.6 minutes for ARC1779 compared with 5.5 minutes for placebo. Using Cox proportional hazards embolic signals occurred statistically significantly later on ARC1779 (P=0.007). Reduced embolic signals counts were correlated with inhibition of von Willebrand factor activity (P=0.03). Increased perioperative bleeding and anemia were seen with ARC1779.
Conclusions:von Willebrand factor inhibition reduces thromboembolism in humans. It may play a role in treatment of stroke and myocardial ischemia. The extent to which bleeding complications occur in nonoperated patients needs to be assessed in further studies. Clinical Trial Registration- URL: http://clinicaltrials.gov. Unique identifier: NCT00742612.
Referred From: https://www.ncbi.nlm.nih.gov/pubmed/21700934
Author(s): No authors listed
Author(s): Muir KW
Author(s): Petty GW, Brown RD Jr, Whisnant JP, Sicks JD, O'Fallon WM, et al.
Author(s): Petty GW, Brown RD Jr, Whisnant JP, Sicks JD, O'Fallon WM, et al.
Author(s): Hacke W, Kaste M, Bluhmki E, Brozman M, Dávalos A, et al.
Author(s): Molina CA
Author(s): Lapchak PA, Araujo DM, Song D, Zivin JA
Author(s): Moskowitz MA, Lo EH, Iadecola C
Author(s): Lapchak PA, Araujo DM
Author(s): De Meyer SF, Stoll G, Wagner DD, Kleinschnitz C
Author(s): Bath PM, Blann A, Smith N, Butterworth RJ
Author(s): Liu Y, Jacobowitz DM, Barone F, McCarron R, Spatz M, et al.
Author(s): Savage B, Almus-Jacobs F, Ruggeri ZM
Author(s): Dong JF, Moake JL, Nolasco L, Bernardo A, Arceneaux W, et al.
Author(s): André P, Denis CV, Ware J, Saffaripour S, Hynes RO, et al.
Author(s): Siedlecki CA, Lestini BJ, Kottke-Marchant KK, Eppell SJ, Wilson DL, et al.
Author(s): Stoll G, Kleinschnitz C, Nieswandt B
Author(s): Kleinschnitz C, Pozgajova M, Pham M, Bendszus M, Nieswandt B, et al.
Author(s): Ni H, Denis CV, Subbarao S, Degen JL, Sato TN, et al.
Author(s): Kleinschnitz C, De Meyer SF, Schwarz T, Austinat M, Vanhoorelbeke K, et al.
Author(s): Lapchak PA
Author(s): Turner RJ, Jickling GC, Sharp FR
Author(s): Lapchak PA, Araujo DM, Zivin JA
Author(s): Zivin JA, Fisher M, DeGirolami U, Hemenway CC, Stashak JA
Author(s): Lapchak PA, Wei J, Zivin JA
Author(s): Zivin JA, Lyden PD, DeGirolami U, Kochhar A, Mazzarella V, et al.
Author(s): Zivin JA, Waud DR
Author(s): Kawaguchi M, Furuya H, Patel PM