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BioWorld - Friday, January 9, 2026
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BioWorld Asia, China
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Beigene and BMS in dispute over Abraxane deal termination in China

Oct. 19, 2021
By David Ho and Doris Yu
Beigene Ltd., which in 2019 parlayed exclusive rights to distribute and promote Abraxane (paclitaxel) in China into more than $111 million in revenue, is contesting Celgene parent Bristol Myers Squibb Co.’s cancellation of the deal in arbitration proceedings at the International Chamber of Commerce.
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IPO, coins, financial chart

Abbisko raises $226M in Hong Kong IPO to develop new solid tumor treatment

Oct. 19, 2021
By Doris Yu
Abbisko Cayman Ltd. has raised $226 million through an IPO in Hong Kong, where it launched with an initial price of HK$12.46 (US$1.60) per share. The company, doing business as Abbisko Therapeutics, plans to use about a third of the proceeds for research and development of its lead candidate, ABSK-091, as a potential treatment for multiple solid tumors.
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Liver and DNA

Hansoh and Olix ink $450M+ liver-focused siRNA therapeutics deal for greater China

Oct. 19, 2021
By Gina Lee and Doris Yu
In a deal that could be worth more than $450 million, Olix Pharmaceuticals Inc. and Hansoh Pharmaceutical Group Co. Ltd. have agreed to discover, develop, and commercialize siRNA therapeutics for various liver-based targets implicated in cardiovascular, metabolic, and other indications.
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siRNA bound to mRNA

Silence reaches China with siRNA deal worth up to $1.3B

Oct. 19, 2021
By Cormac Sheridan
DUBLIN – Silence Therapeutics plc has entered the Chinese market through a partnering deal with Hansoh Pharmaceutical Group Co. Ltd. that involves developing short interfering RNA (siRNA) drugs against three undisclosed targets. The London-based firm is getting $16 million up front and could earn as much as $1.3 billion in development, regulatory and commercial milestones across the alliance. It will also receive tiered sales royalties, ranging from low double digits to mid-teens in percentage terms.
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Antibody-drug conjugate

Third ADC candidate with Synaffix’s tech enters clinic as Miracogen kicks off phase I

Oct. 12, 2021
By David Ho
It looks like Shanghai Miracogen Inc.’s antibody-drug conjugate (ADC) partnership with Synaffix BV is paying off as MRG-004A, an ADC designed to treat solid tumors, has entered a U.S. phase I/II trial to treat solid tumors.
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Brii Bio shares interim data on antibody combination therapy for SARS-CoV-2

Oct. 12, 2021
By David Ho
Brii Biosciences Ltd. shared interim data from a phase III trial of its neutralizing monoclonal antibody (mAb) combination therapy for SARS-CoV-2, BRII-196 and BRII-198, that showed a 78% reduction in the risk of hospitalization or death in patients receiving single dose of the cocktail.
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CBMG’s facility in Shanghai

CBMG bags $120M in its first financing since going private, funds to benefit CAR T candidates

Oct. 5, 2021
By Gina Lee
Cell therapy developer Cellular Biomedicine Group Inc. (CBMG) completed a $120 million series A financing, its first since becoming a private company. The funds will benefit the U.S. and China-based firm’s CAR T pipeline.
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Skin irritation on hands

Union strikes $267M deal with Innovent to develop Otezla challenger in China

Sep. 28, 2021
By Richard Staines
Denmark’s Union Therapeutics A/S has begun a strategic collaboration with Innovent Biologics Inc. over orismilast, a next-generation oral PDE4 inhibitor for inflammatory dermatology conditions that could compete directly with Amgen Inc.’s psoriasis blockbuster, Otezla (apremilast). At the same time, the company is looking for partners in the medium term to develop the drug in the rest of the world as it bids to take on Amgen and other dermatology players such as Bristol-Myers Squibb Co.
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Lung cancer illustration

Cstone presents positive phase III data of sugemalimab for NSCLC

Sep. 28, 2021
By Doris Yu
Cstone Pharmaceuticals Co. Ltd. released positive data from the phase III trial, Gemstone-302, of sugemalimab plus chemotherapy for the first-line treatment of patients with stage IV squamous and non-squamous non-small cell lung cancer.
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FDA accepts Beigene’s first filing outside China; BLA seeks nod for anti-PD-1 tislelizumab

Sep. 21, 2021
By Doris Yu
The FDA has accepted for review Novartis AG and Beigene Ltd.’s BLA filing for the anti-PD-1 monoclonal antibody tislelizumab.
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