FDA
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Antengene Announces 2024 Full-Year Financial Results, Proprietary Programs Advancing to Pivotal Trials with Accelerating Multi-market Revenue Ramp Up
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Antengene Initiates Phase II Dose Expansion Study of Claudin 18.2 ADC ATG-022 in China and Australia
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Antengene Announces ATG-101 Granted Orphan Drug Designation by the U.S. FDA
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Antengene Announces IND Approval in China for a Phase II Study of Eltanexor (ATG-016) in Patients with High-Risk Myelodysplastic Syndromes
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Antengene Presents Results of Phase 1b TOUCH Trial of Selinexor for the Treatment of T and NK-Cell Lymphoma at the 2021 American Society of Hematology (ASH) Annual Meeting
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Antengene Announces Approval of the Phase II Study of Selinexor for the Treatment of Myelofibrosis in China
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Antengene Announces Selinexor Added to Multiple Treatment Regimens in 2021 CSCO Guidelines
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