首页> 外文期刊>Journal of infusion nursing: the official publication of the Infusion Nurses Society >Assessment and implication of the allergic sensitivity to a single dose of recombinant human hyaluronidase injection: a double-blind, placebo-controlled clinical trial.
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Assessment and implication of the allergic sensitivity to a single dose of recombinant human hyaluronidase injection: a double-blind, placebo-controlled clinical trial.

机译:对单剂量重组人透明质酸酶注射液过敏敏感性的评估及其意义:一项双盲,安慰剂对照的临床试验。

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摘要

Animal-extracted injectable hyaluronidases have been used safely for more than 50 years to increase the dispersion and absorption of coadministered drugs and fluids; however, concern still exists about the allergic and immunological risks of these products. Hylenex recombinant, a novel formulation of recombinant human hyaluronidase, has been developed as an alternative to these animal-derived hyaluronidases. Because recombinant human hyaluronidase is a human (nonforeign) protein manufactured into a purer preparation than the animal extracts, it is expected to convey reduced allergic and immunologic risks. The recombinant human hyaluronidase product was well tolerated in this double-blind, placebo-controlled, single-dose study. No allergic reactions were observed among the 100 volunteer subjects who were injected intradermally. These findings supported the US Food and Drug Administration approval of the recombinant human hyaluronidase product.
机译:动物提取的注射用透明质酸酶已经安全使用了50多年,以增加共同给药的药物和液体的分散和吸收。但是,仍然担心这些产品的过敏和免疫风险。已经开发了重组人透明质酸酶的新型制剂Hylenex重组体,以替代这些动物衍生的透明质酸酶。由于重组人透明质酸酶是一种比动物提取物更纯净的人(非外源)蛋白质,因此有望降低过敏和免疫风险。在这项双盲,安慰剂对照,单剂量研究中,重组人透明质酸酶产品具有良好的耐受性。在皮内注射的100名志愿者受试者中未观察到过敏反应。这些发现支持了美国食品药品监督管理局对重组人透明质酸酶产品的批准。

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