1차 출처 기록
회사는 PROSERA 데이터 전체를 논의하기 위해 2026년 6월 중순 FDA와 대면 Pre-NDA Type B 미팅을 확정했다고 밝혔다. 미팅 결과에 따라 Gossamer는 2026년 9월 PAH 대상 seralutinib NDA를 제출할 계획이다. 승인될 경우 2027년 3분기 내 승인이 가능할 수 있다.
EX-99.1 4 goss-20260518xexx991xearni.htm EX-99.1 Document Exhibit 99.1 Gossamer Bio Announces First Quarter 2026 Financial Results and Provides Business Update - FDA Confirms In-Person Pre-NDA Type B Meeting in Mid-June - - Positive PROSERA CT FRI Results Demonstrated Multiple Statistically Significant Treatment Effects, Including Novel Signals Correlated with Clinical Outcomes - - Gossamer Announces Commencement of Exchange Offer and Consent Solicitation for Outstanding 5.00% Convertible Senior Notes Due 2027 - - Cash, cash equivalents and marketable securities totaled $99 million as of March 31 - SAN DIEGO—(BUSINESS WIRE)— May 18, 2026 — Gossamer Bio, Inc. (Nasdaq: GOSS), a clinical-stage biopharmaceutical company focused on the development and commercialization of seralutinib for the