一次情報の記録
FDAはGrace TherapeuticsのGTx-104(ニモジピン)新薬承認申請を正式に受理し、審査を開始した。PDUFA目標アクション日は2026年4月23日に設定された。この受理により、2023年の残存私募ワラントも失効した。
EX-99.1 2 ef20057547_ex99-1.htm EXHIBIT 99.1 Exhibit 99.1 Grace Therapeutics、GTx-104の新薬承認申請がFDA正式審査受理を受け、普通株式ワラント行使により約400万ドルの資金を確保 Princeton, NJ, October 23, 2025 (GLOBE NEWSWIRE)—Grace Therapeutics, Inc. (Nasdaq: GRCE) (Grace Therapeutics or the Company), a late-stage, biopharma company advancing GTx-104, a clinical-stage, novel, injectable formulation of nimodipine being developed for I . V . infusion to address significant unmet medical needs in aneurysmal subarachnoid hemorrhage (aSAH) patients , today announced it has secured approximately $4.0 million in additional funding through exercises of common warrants that were previously issued in a private placement that the Company closed in Sep