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PureTech Health社、LYT-200が第1b相臨床試験で「強力な」抗白血病活性を示したと発表

-- ピュアテック・ヘルス(PRTC)は水曜日、再発・難治性の高リスク骨髄異形成症候群および再発・難治性の急性骨髄性白血病の重度前治療患者を対象としたLYT-200の第1b相臨床試験の主要結果が、「強力な」抗白血病活性と「良好な」安全性プロファイルを示したと発表した。 同社によると、LYT-200と低メチル化剤の併用療法は、完全寛解、移植への橋渡し、および持続的な臨床効果をもたらした。 また、LYT-200は、試験したすべてのコホートおよび用量レベルにおいて一貫した安全性プロファイルを示したという。 同社によると、傘下のギャロップ・オンコロジー部門は、再発・難治性の高リスク骨髄異形成症候群を対象とした第2相臨床試験の推奨用量を決定し、試験デザインについて米国食品医薬品局(FDA)と協議する予定である。

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