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Immunome社、第3相臨床試験データに基づきVaregacestatのNDAを提出

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-- イムノーム(IMNM)は水曜日、成人デスモイド腫瘍患者を対象とした経口治療薬候補であるバレガセスタットについて、米国食品医薬品局(FDA)に新薬承認申請(NDA)を提出したと発表した。 同社によると、この申請は、プラセボ群と比較して無増悪生存期間が有意に改善し、病勢進行または死亡のリスクが84%減少、客観的奏効率が56%であった第3相RINGSIDE試験の良好な結果に基づいている。 同社はまた、同試験の詳細なデータは2026年の米国臨床腫瘍学会(ASCO)年次総会で発表される予定であると付け加えた。 イムノームの株価は水曜日の取引で2.7%下落した。

Price: $23.18, Change: $-0.53, Percent Change: -2.24%

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