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BioWorld - Friday, April 24, 2026
Home » Hutchmed Ltd.

Articles Tagged with ''Hutchmed Ltd.''

China and U.S. flags

China issues new audit rules and weighs giving U.S. regulators full access to audits

April 7, 2022
By Doris Yu
The China Securities Regulatory Commission (CSRC) has issued draft rules to permit U.S. auditors to examine U.S.-listed Chinese companies on April 2, 2022, following a provisional list by the U.S. SEC.
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Three China firms named to US SEC list under HFCAA

March 15, 2022
Three U.S.-listed China-based biopharmas were among five companies named this week by the U.S. SEC for reportedly failing to submit necessary accounting reports under the Holding Foreign Companies Accountable Act (HFCAA).
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SEC identifies firms for tougher audits, including three biopharmas

March 15, 2022
By Gina Lee
The U.S. Securities and Exchange Commission (SEC) recently issued a provisional list of five U.S.-listed Chinese companies that reportedly failed to submit necessary accounting reports required under Holding Foreign Companies Accountable Act. The list included three biopharmas: Beigene Ltd., Hutchmed Ltd., and Zai Lab Ltd.
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SEC identifies firms for tougher audits, including three biopharmas

March 14, 2022
By Gina Lee
The U.S. Securities and Exchange Commission (SEC) recently issued a provisional list of five U.S.-listed Chinese companies that reportedly failed to submit necessary accounting reports required under Holding Foreign Companies Accountable Act. The list included three biopharmas: Beigene Ltd., Hutchmed Ltd., and Zai Lab Ltd.
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Three China firms named to US SEC list under HFCAA

March 11, 2022
Three U.S.-listed China-based biopharmas were among five companies named this week by the U.S. SEC for reportedly failing to submit necessary accounting reports under the Holding Foreign Companies Accountable Act (HFCAA).
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Lung cancer illustration

Hutchmed receives $15M from Astrazeneca to start late-stage trial of Orpathys with Tagrisso

March 8, 2022
By Doris Yu

Hutchmed Ltd. has received a $15 million milestone payment from Astrazeneca plc for initiating a phase III trial testing the Hutchmed c-Met inhibitor Orpathys (savolitinib) in combination with Astrazeneca’s Tagrisso (osimertinib) in EGFR-mutated non-small-cell lung cancer.


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Hutchmed receives $15M from Astrazeneca to start late-stage trial of Orpathys with Tagrisso

March 7, 2022
By Doris Yu

Hutchmed Ltd. has received a $15 million milestone payment from Astrazeneca plc for initiating a phase III trial testing the Hutchmed c-Met inhibitor Orpathys (savolitinib) in combination with Astrazeneca’s Tagrisso (osimertinib) in epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC) for patients with mesenchymal epithelial transition receptor (MET) driven tumors.  


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Prices for state covered drugs in China to be slashed by an average of 61.7%

Dec. 6, 2021
By Doris Yu
Pharmaceutical companies in China will cut the prices for more than five dozen drugs by an average of 61.7% to get them on the latest version of the country’s National Drug Reimbursement List. The National Healthcare Security Administration released the new list on Dec. 3, 2021. The new list includes 74 new drugs, the vast majority of which are branded products without generic versions in China. Only seven of the new drugs on the list have generic versions.
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Opportunity compass with Chinese flag

Hutchmed gains China rights for Epizyme’s Tazverik in $310M pact

Aug. 10, 2021
By David Ho
Hutchmed Ltd. has struck a deal for Epizyme Inc.’s anticancer therapy Tazverik (tazemetostat) that could bring the latter up to $310 million. The agreement gives Hutchmed rights to research, develop, manufacture and commercialize Tazverik in greater China, which covers mainland China, Hong Kong, Macau and Taiwan.
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Hutchmed debuts in Hong Kong with $537M IPO, shares jump 53%

June 30, 2021
By Elise Mak and Angie Ling
Hutchmed Ltd., already listed in the U.S. and London, returned to home soil June 30 for a third IPO on the Hong Kong Stock Exchange that reaped HK$4.17 billion (US$537.2 million). The Hong Kong-based company is currently looking to score its first FDA approval to tap the U.S. market after three China approvals.
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