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Clarity Pharmaceuticals社、米国FDAとの会合後、神経内分泌腫瘍を対象とした第3相臨床試験を開始へ

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-- クラリティ・ファーマシューティカルズ(ASX:CU6)は、米国食品医薬品局(FDA)との最終段階会議が成功裏に終了したことを受け、神経内分泌腫瘍を対象とした銅-64-SARTATEの第3相臨床試験を開始すると、木曜日にオーストラリア証券取引所に提出した書類で明らかにした。 同社はこの試験に約70名の被験者を募集する予定だ。 また、クラリティは、米国とオーストラリアで、根治的前立腺摘除術を受ける高リスク前立腺がん患者を対象とした、銅-64-SAR-bisPSMAを用いた陽電子放出断層撮影(PET)イメージングの第3相臨床試験の被験者募集も行っていると、提出書類で述べている。同社は約383名の被験者を募集する予定だ。 この試験では、骨盤リンパ節内の前立腺がんを検出する際の銅-64-SAR-bisPSMA PETの診断性能を評価すると、提出書類には記載されている。 クラリティ・ファーマシューティカルズの株価は、木曜日の直近の取引で約2%下落した。

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