-- 根據週四提交給澳洲證券交易所的文件，Clarity Pharmaceuticals（ASX：CU6）在與美國食品藥物管理局（FDA）成功舉行階段結束會議後，將啟動一項針對神經內分泌腫瘤的銅-64-SARTATE的註冊性3期臨床試驗。 該公司計劃招募約70名受試者參與試驗。 文件還顯示，Clarity正在美國和澳洲招募受試者，進行一項針對高風險前列腺癌患者在根治性前列腺切除術前使用銅-64-SAR-bisPSMA進行正電子發射斷層掃描（PET）成像的註冊性3期臨床試驗。該公司計劃招募約383名受試者。 文件稱，該試驗將評估銅-64-SAR-bisPSMA PET在檢測骨盆腔淋巴結內前列腺癌的診斷效能。 Clarity Pharmaceuticals的股價在周四的交易中下跌了近2%。
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