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European community and US-FDA approval of recombinant human antithrombin produced in genetically altered goats.

机译:欧洲共同体和美国食品和药物管理局批准了在转基因山羊中生产的重组人抗凝血酶。

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摘要

Thrombin and factor Xa play a central role in thrombogenesis in both medical and surgical patients. Antithrombin (AT) is the key inhibitor, which controls the action of these enzymes in hypercoagulable states. The AT concentrates prepared from human blood have been used to treat patients with thrombotic disorders and heparin resistance. The AT concentrates are prepared from pooled human plasma and beside limited supply, suffer from viral and other biological contaminants. The availability of recombinant human AT (rhAT) obtained from genetically engineered goats provide a biologically equivalent product that can be used in practically all indications where human AT is indicated including heparin resistance. Moreover, because of its high affinity to heparin and related drugs, recombinant AT can also be developed in further indications. On review of the preclinical and clinical data on the safety and efficacy, the European Union and U.S. Food and Drug Administration (US-FDA) have recently approved the use of rhAT in specified clinical indications.
机译:凝血酶和Xa因子在医学和外科手术患者的血栓形成中起着核心作用。抗凝血酶(AT)是关键抑制剂,可在高凝状态下控制这些酶的作用。由人血制备的AT浓缩物已用于治疗血栓形成障碍和肝素抵抗性患者。 AT浓缩物由人血浆汇集而成,除了供应有限外,还受到病毒和其他生物污染物的侵害。从基因工程山羊获得的重组人AT(rhAT)的可用性提供了生物学上等效的产品,几乎可以用于指示人AT的所有适应症中,包括肝素耐药性。而且,由于其对肝素和相关药物的高亲和力,重组AT也可以用于进一步的适应症。在审查有关安全性和有效性的临床前和临床数据后,欧盟和美国食品药品监督管理局(US-FDA)最近批准在特定的临床适应症中使用rhAT。

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