บันทึกจากแหล่งปฐมภูมิ
FDA accepted the NDA for GTx-104 (nimodipine IV) for formal review on August 22, 2025. The agency set a PDUFA target action date of April 23, 2026 for the aSAH indication. The submission is supported by the completed Phase 3 STRIVE-ON safety trial.
EX-99.1 2 ef20058656_ex99-1.htm EXHIBIT 99.1 Exhibit 99.1 Grace Therapeutics Announces Second Quarter 2026 Financial Results, Provides Business Update Announced U.S. Food and Drug Administration (FDA) Acceptance for Review of New Drug Application (NDA) for GTx-104 FDA Established April 23, 2026 as PDUFA Target Date for Review of Submission Seeking Approval for GTx-104 in the Treatment of Patients with aneurysmal Subarachnoid Hemorrhage (aSAH) Phase 3 STRIVE-ON Safety Trial Data Presented at 2025 Neurocritical Care Annual Meeting Granted Sixth U.S. Patent Covering IV Dosing Regimen for GTx-104 Princeton, NJ, November 13, 2025 (GLOBE NEWSWIRE)—Grace Therapeutics, Inc. (Nasdaq: GRCE) (Grace Therapeutics or the Company), a late-stage, biopharma company advancing GTx-104, a clinical-st
Grace Therapeutics: ผลการทดลอง STRIVE-ON Phase 3 ได้รับการยอมรับสำหรับโปสเตอร์ AAN 2026
Grace Therapeutics ได้รับสิทธิบัตรสหรัฐฯ ฉบับที่หกสำหรับระบบการให้ยา GTx-104 ทางหลอดเลือดดำ