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Patients in cohorts 1.11 and 1.12 (currently lacking detectable cancer) will undergo the collection at least 4 weeks after conclusion of therapy. In ...
Patients in cohorts 1.11 and 1.12 (currently lacking detectable cancer) will undergo the collection at least 4 weeks after conclusion of therapy. In addition to ...
美国食品和药品管理局批准的处方药; 与健康有关的消费品; 健身产品或服务; 医疗产品或器械; 药房(零售和在线药房,VIPPS 计划仅适用于在线药房 ...
Scottsdale/Phoenix, Ariz. This is a phase I, multicenter, open-label, dose-escalation study of cevostamab (BFCR4350A) administered as a single agent by IV ...
Rochester, Minn. A study to compare electrophysiologic activity of epidural stimulation and dorsal root ganglion stimulation, as well as quantify changes in ...
Jacksonville, Fla. The purpose of this study is to assess the safety of a specific treatment regimen (protein-bound Paclitaxel, Cisplatin, And Gemcitabine (GCN)) ...
了解更多关于这项血液检查的信息,其检查的是一种称为血红蛋白的蛋白质。水平偏低是红细胞计数低(也称为贫血)的标志。
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