Oral session:ATG-008 (mTORC1/2 Inhibitor) combined with PD-1 antibody in Phase II studies for cervical cancer "Antengene", SEHK: 6996.HK), a leading innovative, commercial-stage global biopharmaceutical company dedicated to discovering, developing and commercializing first-in-class and/or best-in-class medicines for cancer, today announced the presentation of four abstracts (including one oral presentation and three poster presentations) at the 2024 American Society for Clinical Oncology (ASCO) Annual Meeting, taking place from May 31st to June 4th at the McCormick Place Convention Center in Chicago, IL, the United States.
Details of the Oral Presentation:
Session: Clinical Science Symposium – Stronger Together: Novel Combinations Across the Gynecologic Cancer Spectrum Time: 1:15 PM - 2:45 PM (Central Daylight Time)
2:15 AM - 3:45 AM, June 2, 2024 (Beijing Time)
Details of the Poster Presentations:
Session: Developmental Therapeutics—Immunotherapy
Time: 9:00 AM - 12:00 PM (Central Daylight Time)
10:00 PM, June 1 - 1:00 AM, June 2, 2024 (Beijing Time)
(Claudin 18.2 Antibody-drug Conjugate)
Session: Developmental Therapeutics—Molecularly Targeted Agents and Tumor Biology Time: 9:00 AM - 12:00 PM (Central Daylight Time)
10:00 PM, June 1 - 1:00 AM, June 2, 2024 (Beijing Time)
Time: 9:00 AM - 12:00 PM (Central Daylight Time)
10:00 PM, June 3 - 1:00 AM, June 4, 2024 (Beijing Time)
"Antengene", SEHK: 6996.HK) is a leading commercial-stage R&D-driven global biopharmaceutical company focused on the discovery, development, manufacturing and commercialization of innovative first-in-class/best-in-class therapeutics for the treatment of hematologic malignancies and solid tumors, in realizing its vision of "Treating Patients Beyond Borders".
Since 2017, Antengene has built a pipeline of 9 oncology assets at various stages going from clinical to commercial, including 6 with global rights, and 3 with rights for the APAC region. To date, Antengene has obtained 29 investigational new drug (IND) approvals in the U.S. and Asia, and submitted 10 new drug applications (NDAs) in multiple Asia Pacific markets, with the NDA for XPOVIO® (selinexor) already approved in Mainland of China, Taiwan China, Hong Kong China, Macau China, South Korea, Singapore and Australia. Forward-looking statements
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For more information, please contact:
E-mail: [email protected]
E-mail: [email protected]