原始来源记录
FDA 于 2025-09-22 针对 NDA 209531/S-016 签发了完整回复函。
‘4 ¢ BN U.S. FOOD & DRUG ADMINISTRATION NDA 209531/S-016 COMPLETE RESPONSE Biogen, Inc. Attention: Charlene Wheeler, MSHS Director, Global Regulatory Sciences 225 Binney Street Cambridge, MA 02142 Dear Charlene Wheeler: Please refer to your su mental new drug application (SNDA) for Spinraza (nusinersen) injection. This “Prior Approval” efficacy supplement to your application proposes revisions throughout the Prescribing Information (PI) regarding a completed clinical study [Study 4 (NCT04089566)] to provide support for inclusion of an additional higher dosing regimen. Two corresponding additional strength presentations [28 mg/5 mL (5.6 mg/mL) and 50 mg/5 mL (10 mg/mL)] were proposed for administration of the new dosing regimen. This sNDA also proposes revisions to the Pediatric Use