1차 출처 기록
FDA가 후천성 시상하부 비만에 대한 setmelanotide의 sNDA를 수락하고 우선 심사(Priority Review)를 부여했습니다. 2025년 12월 20일의 PDUFA 목표일이 지정되어, 새로운 적응증에 대한 단기 규제 결정 시점이 확정되었습니다.
EX-99.1 2 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)