-- トレンドラインズ(SGX:42T)の子会社であるベンシカ・メディカルは、同社の薬剤送達システム「VixE」の第2相臨床試験開始について、米国食品医薬品局(FDA)の承認を取得した。シンガポール証券取引所への月曜日の提出書類で明らかになった。 医療・その他サービス企業である同社の株価は、火曜日の取引で約5%上昇した。 この針を使わない薬剤送達システムは、過活動膀胱の治療薬として開発されており、第2相試験では米国と欧州で約210人の患者を対象に試験を実施する予定だ。
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