บันทึกจากแหล่งปฐมภูมิ
Following positive Type B meetings, the FDA confirmed that integrated interventional and natural history data could serve as an adequate and well-controlled study supporting accelerated approval. The company now plans to submit the BLA for TA-ERT in Q4 2026, with potential eligibility for a Rare Pediatric Disease Priority Review Voucher.
EX-99.1 6 sprb-ex99_1.htm EX-99.1 EX-99.1 Exhibit 99.1 Spruce Biosciences Reports Full Year 2025 Financial Results and Provides Corporate Updates Following Positive Type B Meetings with the FDA, BLA Submission for TA-ERT for the Treatment of Sanfilippo Syndrome Type B (MPS IIIB) on Track for the Fourth Quarter of 2026 Appoints Dale Hooks as Chief Commercial Officer, Strengthening the Company’s Commercial Capabilities in Preparation for a Potential Launch of TA-ERT Secured up to $50 Million in Growth Capital from Avenue Capital Group South San Francisco, Calif. – March 9, 2026 – Spruce Biosciences, Inc. (Nasdaq: SPRB), a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for neurological disorders with significant unmet medical need, today
Spruce Biosciences: การยื่น BLA ของ TA-ERT ยังเป็นไปตามแผนในไตรมาส 4 ปี 2026
Spruce Biosciences: FDA อนุมัติ Breakthrough Therapy Designation ให้ TA-ERT สำหรับ MPS IIIB