与关键相互作用药物同时使用阿皮克萨班的临床影响
Nicholas Favatella1, David Dalton1, Wonkyung Byon2
1Bristol Myers Squibb, Princeton, NJ, USA.
Clinical pharmacology in drug development
|July 24, 2024
概括
作为XA因子抑制剂的阿皮克萨班在与相互作用的药物一起使用时保持了有利的益处风险概况. 本综述考察了阿皮克萨班的使用情况.
科学领域:
- 药理学 药理学是指药理学的学科.
- 临床医学 临床医学
- 药物相互作用 药物相互作用
背景情况:
- 抗凝剂的选择需要仔细评估益处与风险,特别是在并发症和药物相互作用的情况下.
- 阿皮克萨班是一种广泛使用的选择性XA因子抑制剂,用于抗凝血.
研究的目的:
- 评估阿皮克萨班与相互作用的药物同时使用时的益处风险概况.
- 审查apixaban在特定患者群体中的使用,包括那些患有癌症相关的血栓栓塞和COVID-19的患者.
主要方法:
- 来自多个药物开发阶段的临床数据的叙述性综述.
- 来自第三期ARISTOTLE试验 (NCT00412984) 的子组分析,检查P-糖蛋白和CYP3A4抑制剂/诱导剂的同时使用.
主要成果:
- 阿皮克萨班与相互作用的药物显示出可管理的益处风险概况.
- 证据支持在患有癌症相关血栓栓塞和COVID-19的患者中使用阿皮克萨班.
结论:
- 阿皮克萨班的益处风险概况即使在同时服用药物时也仍然有利.
- 临床数据支持阿皮克萨班在复杂的患者场景中的实用性,包括癌症和COVID-19.
相关概念视频
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
1.2K
Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
1.2K
Factors Affecting Protein-Drug Binding: Drug Interactions
125
Drug interactions are a critical aspect of pharmacology and can occur when two or more drugs compete for the same binding site. This competition can result in one drug displacing another, altering the effect of the displaced drug. Drug interactions are complex processes that rely heavily on how much of the displacer drug is present and how strongly it can bind to the same sites as the displaced drug.
Displacement interactions can have varying outcomes, ranging from toxicity to virtually...
Displacement interactions can have varying outcomes, ranging from toxicity to virtually...
125
Anticoagulant Drugs: Low-Molecular-Weight Heparins
663
Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
663
Combined Effects of Drugs: Antagonism
8.4K
The combined effects of drugs can result in various interactions, of which an important type is antagonism. Antagonism is a mechanism where one drug inhibits or counteracts the effects of another drug. Antagonism can occur through various means, including receptor binding, allosteric modulation, functional interaction, chemical reactions, and pharmacokinetic processes.
The most common type is receptor antagonism, where one drug acts as an antagonist to block the effects of another drug by...
The most common type is receptor antagonism, where one drug acts as an antagonist to block the effects of another drug by...
8.4K
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
507
Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
507
Factors Affecting Drug Response: Overview
1.9K
When it comes to infants and young children, they are typically administered smaller doses of medication in comparison to adults. This is primarily because their organ functions still need to fully develop, meaning their bodies are not as efficient at metabolizing or eliminating drugs. Additionally, their blood-brain barrier is more permeable than in adults. As a result, high concentrations of drugs can easily penetrate the central nervous system (CNS), potentially leading to neurological...
1.9K


