1차 출처 기록

결정급FDA 승인

Nuvation Bio: IBTROZI(taletrectinib), 진행성 ROS1+ NSCLC에 대해 2025년 6월 승인

The 8-K confirms U.S. FDA approval of IBTROZI on June 11, 2025 for advanced ROS1+ NSCLC (line-agnostic). The company reports 204 new patient starts in Q3 2025 and 80% payor coverage, establishing commercial traction. Updated August 2025 data show median DOR of 50 months in TKI-naïve patients, supporting a planned supplemental NDA filing by year-end 2025.

핵심 사실

제출
2025년 11월 26일 PM 01:34
이벤트
FDA 승인
방향
긍정적
출처
SEC 8-K
신뢰도
출처 확인
cORR TKI 미경험
89%
보험 적용률
80%
TKI 미경험 중앙 DOR
50개월
2025년 3분기 시작 환자
204

출처 발췌

EX-99.1 2 d82457dex991.htm EX-99.1 EX-99.1 DRIVEN BY SCIENCE FOCUSED ON LIFE November 2025 Exhibit 99.1 Forward-looking statements Certain statements included in this presentation (this “Presentation”) that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied by words such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,” “seem,” “seek,” “future,” “outlook” and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are

SEC 8-K

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학회 발표SEC 8-K
주목
2025년 11월 3일
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Nuvation Bio: IBTROZI의 중앙 DOR이 50개월로 성숙; 204명의 신규 환자 시작

FDA 라벨 업데이트SEC 8-K