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BioWorld - Wednesday, July 1, 2026
Home » Brukinsa

Articles Tagged with ''Brukinsa''

Mantle cell lymphoma

Beone’s BCL2 drug Beqalzi wins FDA nod in mantle cell lymphoma

May 13, 2026
By Jennifer Boggs
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A few months after winning its first regulatory clearance in China, Beone Medicines Inc.’s next-generation BCL2 inhibitor, sonrotoclax, gained the U.S. FDA’s accelerated approval for use in patients with relapsed or refractory mantle cell lymphoma (MCL) following treatment with a BTK inhibitor. The therapy, branded Beqalzi, marks the first BCL2-targeting drug for MCL in the U.S., but the company has pointed to a bigger opportunity in the potential combination with blockbuster BTK drug Brukinsa (zanubrutinib).
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Imbruvica capsules and packaging

BTK inhibitor potential highlighted at ASH 2024

Dec. 10, 2024
By Brian Orelli
At the 66th American Society of Hematology Annual Meeting, a plethora of companies presented clinical trial data highlighting their drugs targeting Bruton tyrosine kinase (BTK) in patients with blood cancers.
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Multiple sclerosis

Et tu, Bruton? New approach in MS gains ground despite Merck partial hold

May 9, 2023
By Randy Osborne
Watchers of the Bruton’s kinase (BTK) inhibitor space may be casting renewed skepticism in that direction after Merck KGaA disclosed April 12 that the U.S. FDA placed a partial clinical hold on the sign-up of more patients in work testing evobrutinib in relapsing multiple sclerosis (MS) – but BTK efforts in MS continue in various quarters.
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Beigene’s zanubrutinib meets primary endpoints in phase III trial to treat chronic lymphocytic leukemia

April 19, 2022
By Doris Yu
Beigene Ltd.’s BTK inhibitor Brukinsa (zanubrutinib) has met the primary endpoints in a phase III trial to treat patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma.
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Beigene’s zanubrutinib meets primary endpoints in phase III trial to treat chronic lymphocytic leukemia

April 13, 2022
By Doris Yu
Beigene Ltd.’s BTK inhibitor Brukinsa (zanubrutinib) has met the primary endpoints in a phase III trial to treat patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma.
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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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EU flag, syringe, capsules

Citing safety worries, EU regulators reject Pfizer’s tanezumab for osteoarthritis pain

Sep. 17, 2021
By Richard Staines
European regulators have rejected Pfizer Inc.’s tanezumab, casting further doubts on whether the FDA will okay the troubled drug that is intended as a non-opioid alternative for osteoarthritis pain.
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Shanghai, China, stock market illustration

With nod for Shanghai listing, Beigene to have shares in U.S., Hong Kong and mainland China

July 1, 2021
By Alfred Romann
Beigene Ltd. got the green light for an IPO on the Shanghai Stock Exchange’s Science and Technology Innovation Board, a specialized board known as the STAR Market, that could be worth around $3 billion. It would make Beigene the first biotech company with listings in the U.S., Hong Kong and mainland China.
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Leukemia illustration

EHA 2021: Beigene reveals positive data of phase III trial on cancer treatments

June 15, 2021
By Sergio Held
Beigene Ltd. unveiled positive interim results from its Alpine phase III trial comparing its small-molecule BTK inhibitor, Brukinsa (zanubrutinib), to Abbvie Inc.’s Imbruvica (ibrutinib), lending validity to one of the company’s most important development programs.
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Leukemia illustration

EHA 2021: Beigene reveals positive data of phase III trial on cancer treatments

June 11, 2021
By Sergio Held
Beigene Ltd. unveiled positive interim results from its Alpine phase III trial comparing its small-molecule BTK inhibitor, Brukinsa (zanubrutinib), to Abbvie Inc.’s Imbruvica (ibrutinib), lending validity to one of the company’s most important development programs.
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