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HUTCHMED Initiates a Japan Bridging Study to Support Surufatinib Registration for Advanced ...

HUTCHMED Initiates a Japan Bridging Study to Support Surufatinib Registration for Advanced ...
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HUTCHMED Initiates a Japan Bridging Study to Support

HUTCHMED Initiates a Japan Bridging Study to Support
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Investegate |Hutchmed China Ltd Announcements | Hutchmed China Ltd: Total Voting Rights


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HUTCHMED's Marketing Authorization Application for Surufatinib Submitted and Validated by the European Medicines Agency


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– EMA commences review of surufatinib for the treatment of advanced neuroendocrine tumors –
– Expands potential global reach of surufatinib, in addition to China where it is already launched, and in the U.S. where it is under review for marketing approval –
HONG KONG, SHANGHAI, China and FLORHAM PARK, N.J., July 15, 2021 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM: HCM; HKEX: 13) today announces that the European Medicines Agency ("EMA") has validated and accepted its marketing authorization application ("MAA") for surufatinib for the treatment of pancreatic and extra-pancreatic (non-pancreatic) neuroendocrine tumors ("NETs"). The EMA's validation confirms that the submission is sufficiently complete and that it is ready to commence the formal review process.

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HUTCHMED Announces First Commercial Sale of ORPATHYS® in China, Triggering a US$25 million ...

HUTCHMED Announces First Commercial Sale of ORPATHYS® in China, Triggering a US$25 million ...
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HUTCHMED Announces First Commercial Sale of ORPATHYS® in China, Triggering a US$25 million Milestone Payment from AstraZeneca

HUTCHMED Announces First Commercial Sale of ORPATHYS® in China, Triggering a US$25 million Milestone Payment from AstraZeneca
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HUTCHMED Announces Full Exercise of the Over-allotment Option of the Global Offering

HUTCHMED Announces Full Exercise of the Over-allotment Option of the Global Offering
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U.S. FDA Accepts Filing of HUTCHMED's NDA for Surufatinib for the Treatment of Advanced Neuroendocrine Tumors

U.S. FDA Accepts Filing of HUTCHMED's NDA for Surufatinib for the Treatment of Advanced Neuroendocrine Tumors
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HUTCHMED Announces the Closing of the Global Offering and the Primary Listing in Hong Kong

HUTCHMED Announces the Closing of the Global Offering and the Primary Listing in Hong Kong
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HUTCHMED Highlights Clinical Data to be Presented at the Upcoming ASCO21 Virtual Scientific Program

HUTCHMED Highlights Clinical Data to be Presented at the Upcoming ASCO21 Virtual Scientific Program
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