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Targeting ticagrelor: a novel therapy for emergency reversal

机译:靶向替卡格雷:紧急逆转的新疗法

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摘要

Newer P2Y12 inhibitors are prescribed in place of clopidogrel for patients with acute coronary syndrome (ACS) and are associated with significant bleeding risks. Currently, limited options exist for the management of life-threatening bleeding or acute reversal for patients on P2Y12 inhibitor therapy, specifically ticagrelor. Various interventions, including platelet transfusion and desmopressin, have been studied for ticagrelor reversal demonstrating limited success. PB2452 is a novel monoclonal antibody which binds to both ticagrelor and its active metabolite resulting in a rapid return of platelet aggregation. PB2452 has been studied in animal models and, most recently, in a Phase I trial in healthy volunteers. In animal models, PB2452 displayed rapid reversal of ticagrelor and its metabolites and return to near normal levels of platelet aggregation within 60 min. In healthy human volunteers, cohorts that received higher dose bolus and infusions of PB2452 over 12–16 h resulted in maximal and sustained reversal of ticagrelor inhibition of platelet aggregation. While it is currently not US Food and Drug Administration approved, future Phase 2 and 3 studies are currently underway that may lead to new directions for patients on ticagrelor therapy who require urgent reversal.
机译:对于患有急性冠脉综合征(ACS)的患者,开具了更新的P2Y12抑制剂以代替氯吡格雷,并伴有明显的出血风险。当前,对于接受P2Y12抑制剂治疗的患者(特别是替卡格雷)的危及生命的出血或急性逆转的治疗存在有限的选择。已经研究了各种干预措施,包括血小板输注和去氨加压素,用于替卡格雷逆转,证明成功有限。 PB2452是一种新颖的单克隆抗体,可与替卡格雷及其活性代谢物结合,从而使血小板聚集迅速恢复。 PB2452已在动物模型中进行了研究,最近在健康志愿者的I期试验中进行了研究。在动物模型中,PB2452在60分钟内显示出替卡格雷及其代谢产物的快速逆转,并恢复到接近正常的血小板聚集水平。在健康的人类志愿者中,在12–16 h内接受更高剂量推注和PB2452输注的人群导致替卡格雷对血小板聚集的抑制作用得以最大程度和持续地逆转。尽管目前尚未获得美国食品药品监督管理局的批准,但正在进行的未来2期和3期研究可能会为接受替卡格雷治疗的需要紧急逆转的患者提供新的指导。

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