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Radiopharm公司称,人体试验结果显示,该放射性治疗候选药物具有“显著”的肿瘤摄取率和良好的安全性。

-- Radiopharm Theranostics(ASX:RAD)周一向澳大利亚证券交易所提交的文件显示,正在进行的0/1期HEAT试验的首批人体试验结果显示,其放射性治疗候选药物镥-177-RAD202在最低剂量30毫居里(mCi)下即可实现“显著”的肿瘤摄取,且安全性良好。 文件指出,器官吸收的辐射剂量在预期和临床可接受的范围内,支持继续增加剂量,同时未观察到剂量限制性毒性或因不良事件导致的治疗中断。 文件还补充道,在接受治疗的前三名患者中,该放射性治疗候选药物的耐受性总体良好,主要出现1至2级的治疗相关不良事件。 Radiopharm Theranostics的股价在周一的交易中上涨超过2%。

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