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首页> 外文期刊>Cancer chemotherapy and pharmacology. >Comparative pharmacokinetics, safety, and tolerability of two sources of ch14.18 in pediatric patients with high-risk neuroblastoma following myeloablative therapy
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Comparative pharmacokinetics, safety, and tolerability of two sources of ch14.18 in pediatric patients with high-risk neuroblastoma following myeloablative therapy

机译:小儿清髓性治疗后高危神经母细胞瘤小儿ch14.18两种来源的比较药代动力学,安全性和耐受性

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摘要

Dinutuximab (Unituxin (TM); ch14.18), a monoclonal antibody against disialoganglioside, improved survival as part of post-consolidation therapy for high-risk neuroblastoma. United Therapeutics Corporation (UTC) assumed ch14.18 production from the National Cancer Institute (NCI); this study evaluates pharmacokinetic comparability, safety, and tolerability of UTC and NCI products.
机译:抗双唾液酸神经节苷脂的单克隆抗体Dinutuximab(Unituxin(TM); ch14.18)作为高危神经母细胞瘤巩固治疗后的一部分提高了生存率。 United Therapeutics Corporation(UTC)假定国家癌症研究所(NCI)生产ch14.18;这项研究评估了UTC和NCI产品的药代动力学可比性,安全性和耐受性。

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