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Nuvation Bio Inc. (NYSE: NUVB) will present updated data on taletrectinib, a ROS1 inhibitor, at the 2024 American Society of Clinical Oncology Annual Meeting. The Phase 2 TRUST-I study will showcase the efficacy and safety of taletrectinib in ROS1-positive non-small cell lung cancer patients in China. Presenter Wei Li, M.D., will discuss the findings on Saturday, June 1, 2024.
Nuvation Bio Inc. (NYSE: NUVB) presenterà dati aggiornati su taletrectinib, un inibitore ROS1, durante il Meeting Annuale 2024 della Società Americana di Oncologia Clinica. Lo studio di Fase 2 TRUST-I evidenzierà l'efficacia e la sicurezza del taletrectinib nei pazienti cinesi affetti da carcinoma polmonare non a piccole cellule ROS1-positivo. Il relatore, il dottor Wei Li, discuterà i risultati sabato 1 giugno 2024.
Nuvation Bio Inc. (NYSE: NUVB) presentará datos actualizados sobre taletrectinib, un inhibidor de ROS1, en la Reunión Anual de la Sociedad Americana de Oncología Clínica de 2024. El estudio de Fase 2 TRUST-I demostrará la eficacia y seguridad de taletrectinib en pacientes chinos con cáncer de pulmón de células no pequeñas positivo a ROS1. El presentador, el Dr. Wei Li, hablará sobre los hallazgos el sábado 1 de junio de 2024.
뉴베이션 바이오 주식회사(NYSE: NUVB)는 2024년 미국 임상 종양학회 연례 회의에서 탈렉트리닙, ROS1 억제제에 대한 최신 데이터를 발표할 예정입니다. 2상 TRUST-I 연구는 중국의 ROS1 양성 비소세포 폐암 환자에서 탈렉트리닙의 효과와 안전성을 보여줄 것입니다. 발표자인 위 리 박사는 2024년 6월 1일 토요일에 연구 결과에 대해 논의할 것입니다.
Nuvation Bio Inc. (NYSE: NUVB) présentera des données mises à jour sur le taletrectinib, un inhibiteur de ROS1, lors de la Réunion Annuelle 2024 de la Société Américaine d'Oncologie Clinique. L'étude de phase 2 TRUST-I mettra en avant l'efficacité et la sécurité du taletrectinib chez des patients chinois atteints d'un cancer du poumon non à petites cellules ROS1-positif. Le présentateur, le Dr Wei Li, discutera des résultats le samedi 1er juin 2024.
Nuvation Bio Inc. (NYSE: NUVB) wird aktualisierte Daten zu Taletrectinib, einem ROS1-Inhibitor, auf der Jahrestagung 2024 der Amerikanischen Gesellschaft für Klinische Onkologie präsentieren. Die Phase-2-Studie TRUST-I wird die Wirksamkeit und Sicherheit von Taletrectinib bei chinesischen Patienten mit ROS1-positivem nicht-kleinzelligem Lungenkrebs hervorheben. Der Redner Dr. Wei Li wird die Ergebnisse am Samstag, den 1. Juni 2024, diskutieren.
Positive
Nuvation Bio Inc. will present updated data on taletrectinib at the 2024 ASCO Annual Meeting
The Phase 2 TRUST-I study will evaluate taletrectinib in ROS1-positive NSCLC patients in China
Presenter Wei Li, M.D., will discuss the efficacy and safety of taletrectinib on June 1, 2024
Negative
None.
NEW YORK--(BUSINESS WIRE)--
Nuvation Bio Inc. (NYSE: NUVB), a late-stage, global biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates, today announced that updated data from the Phase 2 TRUST-I clinical study (NCT04395677) evaluating taletrectinib in patients in China with ROS1-positive non-small cell lung cancer (NSCLC) will be reported in an oral presentation at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting taking place May 31-June 4, 2024 in Chicago, Illinois.
Presentation Overview:
Title: Efficacy and safety of taletrectinib in patients with advanced or metastatic ROS1+ non-small cell lung cancer: The phase 2 TRUST-I study
Presenter: Wei Li, M.D., Department of Medical Oncology, Shanghai Pulmonary Hospital, Thoracic Cancer Institute, Tongji University School of Medicine
Date: Saturday,June 1, 2024
Session Time: 4:30-6:00 p.m. CT/5:30-7:00 p.m. ET
Session: Lung Cancer — Non-Small Cell Metastatic
Abstract: 8520
The materials will be made available on the Publications section of nuvationbio.com the morning of the presentation.
About Taletrectinib
Taletrectinib is an oral, potent, central nervous system-active, selective, next-generation ROS1 inhibitor specifically designed for the potential treatment of patients with ROS1-positive NSCLC.
Taletrectinib is being evaluated for the treatment of patients with ROS1-positive NSCLC in two Phase 2 single-arm pivotal studies: TRUST-I (NCT04395677) in China, and TRUST-II (NCT04919811), a global study.
Taletrectinib has been granted Breakthrough Therapy Designations by both the U.S. Food and Drug Administration (FDA) and China’s National Medical Products Administration (NMPA) for the treatment of patients with advanced or metastatic ROS1-positive NSCLC. Based on results of the TRUST-I clinical study, China’s NMPA has accepted and granted Priority Review Designations to New Drug Applications for taletrectinib for the treatment of adult patients with locally advanced or metastatic ROS1-positive NSCLC who either have or have not previously been treated with ROS1 tyrosine kinase inhibitors (TKIs).
About Nuvation Bio
Nuvation Bio is a late-stage, global biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates. Nuvation Bio’s portfolio of development candidates includes taletrectinib (ROS1), safusidenib (mIDH1), NUV-868 (BET), and NUV-1511 (DDC). Nuvation Bio was founded in 2018 by biopharma industry veteran David Hung, M.D., who previously founded Medivation, Inc., which brought to patients one of the world’s leading prostate cancer medicines. Nuvation Bio has offices in New York, San Francisco, and Shanghai. For more information, please visit www.nuvationbio.com and https://www.linkedin.com/company/nuvationbio/.