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4/26 - 8:30 AM \; \;HUTCHMED Announces Positive CHMP Opinion for Fruquintinib in Previously Treated Metastatic Colorectal Cancer Received by Takeda
4/5 - 4:30 AM \; \;HUTCHMED Highlights Data to be Presented at AACR Congress 2024
4/2 - 1:00 AM \; \;HUTCHMED and Innovent Jointly Announce NDA Acceptance in China for Fruquintinib Combination with Sintilimab for the Treatment of Advanced Endometrial Cancer with Priority Review Status
3/27 - 8:00 PM \; \;HUTCHMED Announces Savolitinib sNDA Accepted in China for Treatment-Nave or Previously Treated Patients with Locally Advanced or Metastatic MET Exon 14 NSCLC
3/21 - 8:00 PM \; \;HUTCHMED Initiates Registration Stage of the ESLIM-02 Phase II/III Trial of Sovleplenib for Warm Antibody Autoimmune Hemolytic Anemia in China
2/28 - 6:30 AM \; \;HUTCHMED Reports 2023 Full Year Results and Provides Business Updates
2/6 - 7:00 PM \; \;HUTCHMED Highlights Presentation of Phase III Data on Fruquintinib in Second-Line Gastric Cancer at ASCO Plenary Series Session
2/2 - 3:30 AM \; \;HUTCHMED Announces that Inmagene Exercises Option to License Two Drug Candidates as Part of Strategic Partnership
2/1 - 3:30 AM \; \;HUTCHMED to Announce 2023 Final Results
1/29 - 11:54 PM \; \;HUTCHMED Receives ELUNATE (fruquintinib) Marketing Approval in Hong Kong for Treatment of Metastatic Colorectal Cancer
1/10 - 7:00 PM \; \;HUTCHMED Announces NDA Acceptance in China for Sovleplenib for the Treatment of Primary Immune Thrombocytopenia with Priority Review Status
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