-- 根据周四提交给澳大利亚证券交易所的文件，Clarity Pharmaceuticals（ASX：CU6）在与美国食品药品监督管理局（FDA）成功举行阶段结束会议后，将启动一项针对神经内分泌肿瘤的铜-64-SARTATE的注册性3期临床试验。 该公司计划招募约70名受试者参与该试验。 文件还显示，Clarity正在美国和澳大利亚招募受试者，开展一项针对高危前列腺癌患者在根治性前列腺切除术前使用铜-64-SAR-bisPSMA进行正电子发射断层扫描（PET）成像的注册性3期临床试验。该公司计划招募约383名受试者。 文件称，该试验将评估铜-64-SAR-bisPSMA PET在检测盆腔淋巴结内前列腺癌方面的诊断性能。 Clarity Pharmaceuticals的股价在周四的交易中下跌了近2%。
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