Registro de fonte primária

Nível de decisãoCarta de resposta completa (CRL)

PTC Therapeutics, Inc. · carta de resposta completa (NDA 220049)

FDA emitiu uma carta de resposta completa para NDA 220049 datada de 2025-08-18.

Fatos principais

Arquivado
18 de ago. de 2025, 00:00
Evento
Carta de resposta completa (CRL)
Direção
Negativo
Fonte
openFDA
Confiança
Com fonte

Trecho da fonte

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

openFDA