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BioWorld - Wednesday, February 4, 2026
Home » Beigene Ltd.

Articles Tagged with ''Beigene 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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Beigene gets first reimbursement in Australia for Brukinsa in mantle cell lymphoma

March 15, 2022
By Tamra Sami
Australians with mantle cell lymphoma (MCL) will now have subsidized access to Beigene Ltd.’s BTK inhibitor, Brukinsa (zanubrutinib), as of March 1, marking the company’s first drug to be listed on Australia’s Prescription Benefits Scheme (PBS).
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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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Remdesivir vial and syringe

With limited options, US FDA aims at omicron by expanding Veklury use

Jan. 24, 2022
By Mari Serebrov
Once again, the U.S. FDA giveth and it taketh away. Just a few days after expanding its approval for Gilead Sciences Inc.’s Veklury (remdesivir) to provide access to more people infected with COVID-19, the FDA essentially shut down the use of two monoclonal antibody (mAb) treatments Jan. 24 that had been authorized to treat mild-to-moderate COVID-19 infections – Regeneron Inc.’s Regen-Cov (Ronapreve in Europe), an antibody cocktail of casirivimab and imdevimab, and Eli Lilly and Co.’s bamlanivimab and etesevimab that are administered together.
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Beigene’s $3.4B Shanghai IPO loses steam on first trading day

Dec. 21, 2021
By Doris Yu
Beigene Ltd.’s listing on the Shanghai STAR Market netted ¥22 million ($3.4 billion) as the company became making it the first biotech firm to be listed on Nasdaq, the Hong Kong Stock Exchange, and the Shanghai STAR Market. But Shanghai shares, initially priced at ¥192.6 each, fizzled quickly, plunging over 16.4% by market close to ¥160.98 on Dec. 15.
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Illustration of cancer cells and immunotherapy treatment

Novartis forges closer links with Beigene, taking $1B option on TIGIT cancer drug

Dec. 21, 2021
By Richard Staines
Novartis AG has forged even stronger links with Beigene Ltd., taking an option on the latter’s late-stage TIGIT inhibitor cancer immunotherapy ociperlimab in a deal worth up to $1 billion.
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Illustration of cancer cells and immunotherapy treatment

Novartis forges closer links with Beigene, taking $1B option on TIGIT cancer drug

Dec. 20, 2021
By Richard Staines
Novartis AG has forged even stronger links with Beigene Ltd., taking an option on the latter’s late-stage TIGIT inhibitor cancer immunotherapy ociperlimab in a deal worth up to $1 billion. Basel, Switzerland-based Novartis will pay the Beijing-based pharma $300 million up front in the option, collaboration and license agreement plus up to $700 million if it exercises its option before late 2023.
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