Rhythm define PDUFA para 20 de dez. de 2025 para sNDA de setmelanotide em HO adquirida
FDA aceitou a sNDA para setmelanotide em obesidade hipotalâmica adquirida e concedeu Revisão Prioritária. Uma data-alvo PDUFA de 20 de dezembro de 2025 foi atribuída, estabelecendo um ponto de decisão regulatória de curto prazo para a nova indicação.
Decisão da FDA (PDUFA) · 20 de mar. de 2026 · Positivo
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EX-99.1
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rytm-20251104xex99d1.htm
EX-99.1
Exhibit 99.1
Rhythm Pharmaceuticals Reports Third Quarter 2025 Financial Results and Business Update
-- Third quarter 2025 net product revenue from global sales of IMCIVREE ® (setmelanotide) of $51.3 million --
-- December 20, 2025 PDUFA goal date set for sNDA for setmelanotide in acquired hypothalamic obesity --
-- Company is on track to report preliminary results from setmelanotide Phase 2 trial in Prader-Willi syndrome in fourth quarter of 2025 --
-- German observational study showed setmelanotide therapy was associated with improvement in measures of MASLD and kidney function in BBS patients --
-- Management to host conference call today at 8:00 a.m. ET --
BOSTON, November 4, 2025 – Rhythm Pharmaceuticals, Inc. (Nasdaq: RYTM)