1차 출처 기록

결정급보완요구서한 (CRL)

PTC Therapeutics, Inc. · 완전 응답 서한 (NDA 220049)

FDA는 2025-08-18에 NDA 220049에 대한 완전 응답 서한을 발행했습니다.

핵심 사실

제출
2025년 8월 18일 AM 12:00
이벤트
보완요구서한 (CRL)
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부정적
출처
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출처 발췌

ADMINISTRATION ¢ YN U.S. FOOD & DRUG NDA 220049 COMPLETE RESPONSE PTC Therapeutics, Inc. Attention: Aparna Geddam, MS Director, Global Regulatory Strategy 500 Warren Corporate Center Drive Warren, NJ 07059 Dear Aparna Geddam: Please refer to your new drug application (NDA) oe or vatiquinone oral capsules, oe We have completed our review of this application, as amended, and have determined that we cannot approve this application in its present form. We have described our reasons for this action below and, where possible, our recommendations to address these issues. CLINICAL/BIOSTATISTICS 1. After a detailed review of your application, we have concluded that the data do not demonstrate substantial evidence of effectiveness (SEE) for vatiquinone in the treatment of Friedreich’s Atax

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