一次情報の記録
同社は2026年第2四半期に150名の患者登録完了を予定し、EMPEROR第3相データの結果発表を2027年半ばに前倒しした。ローリングNDA提出は2027年前半に開始予定。Breakthrough Therapy Designationに基づくFDAとの継続的な協議では、迅速化経路の検討が続けられている。
EX-99.1 2 d36198dex991.htm EX-99.1 EX-99.1 Exhibit 99.1 Stoke Therapeutics Announces Updates to Timelines for the Completion of Enrollment and a Phase 3 Data Readout from the EMPEROR Study of Zorevunersen for the Treatment of Dravet Syndrome — Company now expects to complete enrollment of 150 patients in Q2 2026, with a Phase 3 data readout in mid-2027; Rolling NDA submission planned to initiate in first half 2027— — Discussions with FDA ongoing following recent multidisciplinary meeting; Company continues to explore potential for expedited development, registration and delivery of zorevunersen to patients — – Company to present at 44 th Annual J.P. Morgan Healthcare Conference on Tuesday, January 13, 2026 — BEDFORD, Mass, January 11, 2026 – Stoke Therapeutics, Inc . (Nasdaq: STOK) is
Stoke TherapeuticsがDravet症候群に対するzorevunersenの第3相EMPEROR試験の進捗とFDAとの調整を更新
Stoke Therapeutics、Dravet症候群に対するZorevunersenのNDA計画およびVineland-3解析についてFDAと合意
Stoke Therapeutics、Bo Cumboを取締役に任命、Zorevunersenの2028年初頭のFDA承認の可能性を指摘