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BioWorld - Thursday, June 18, 2026
Home » Topics » Regions » Asia-Pacific

Asia-Pacific
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Lianbio shuttering operations, after rejecting Concentra

Feb. 20, 2024
By Tamra Sami
After Lianbio Co. Ltd. turned away a $465 million acquisition offer from Concentra Biosciences LLC, the China and U.S.-based biotech announced it was selling off its assets and shutting down the company.
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3D dollar sign

Kyowa pays $100M up front for Bridgebio’s infigratinib in Japan

Feb. 20, 2024
By Marian (YoonJee) Chu
Palo Alto, Calif.-based Bridgebio Pharma Inc. will hand over development and sales of its rare bone growth disorder therapy, infigratinib, in Japan to Kyowa Kirin Co. Ltd. under its latest exclusive licensing deal.
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Elderly man with clenched hands holding head

Three strikes for Otsuka’s AVP-786 as it fails in AD-related agitation

Feb. 20, 2024
By Tamra Sami
Otsuka Pharmaceutical Co. Ltd.’s AVP-786 missed the primary endpoint for a third time in a phase III trial for agitation associated with dementia due to Alzheimer’s disease (AD). Two previous phase III trials also failed to show statistical significance for AVP-786.
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Mixed results for Hutchmed’s fruquintinib phase III in gastric cancer

Feb. 20, 2024
By Marian (YoonJee) Chu
Hong Kong’s Hutchmed (China) Ltd. reported mixed phase III results of fruquintinib as a second-line combination therapy for advanced gastric cancer on Feb. 6, with the oral vascular endothelial growth factor receptor inhibitor hitting just one co-primary endpoint.
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FDA accepts Daiichi/Astrazeneca’s BLA for Trop2 lung cancer drug

Feb. 20, 2024
By Tamra Sami
The U.S. FDA has accepted for review Daiichi Sankyo Co. Ltd.’s and Astrazeneca plc’s BLA for datopotamab deruxtecan (dato-dxd) to treat adults with locally advanced or metastatic nonsquamous non-small-cell lung cancer who have received prior systemic therapy.
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Eye illustration

Innovent thyroid eye therapy hits phase III goal, spurs China NDA

Feb. 20, 2024
By Marian (YoonJee) Chu
In a crowded thyroid eye disease (TED) space, Innovent Biologics Inc. reported positive late-stage findings for its TED therapy, IBI-311, spurring the Suzhou, China-based biopharma to file for regulatory approval in China.
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CAR T cells attacking cancer cell

Astellas’ Xyphos teams with Kelonia on cancer drugs in $800M deal

Feb. 16, 2024
By Marian (YoonJee) Chu
San Francisco-based Xyphos Biosciences Inc. is pooling technology platforms with Boston’s Kelonia Therapeutics Inc. in a novel immuno-oncology (I-O) drug discovery deal that could fetch more than $800 million. Xyphos and Kelonia will collaborate to develop a maximum of two in vivo CAR T-cell therapy programs, utilizing both Kelonia’s in vivo gene placement system called iGPS and Xyphos’ Accel technology platform.
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Hands holding gears

Ono inks deals with Shattuck, Numab in autoimmune disease, oncology

Feb. 15, 2024
By Tamra Sami
Ono Pharmaceutical Co. Ltd. inked deals with Shattuck Labs Inc. and Numab Therapeutics AG aimed at bolstering its pipeline in oncology and autoimmune and inflammatory diseases. Ono struck a drug discovery collaboration and option agreement with Shattuck Labs to generate bifunctional fusion proteins for pathways involved in autoimmune and inflammatory diseases. It also signed a global research, development and commercialization deal with Numab for its NM-49, a multispecific antibody designed to activate tumor-associated macrophage phagocytosis for treating cancers.
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SkyLabs CART wearable BP ring

More data supports ‘world’s first’ wearable ring for BP monitoring

Feb. 15, 2024
By Marian (YoonJee) Chu
Sky Labs reported it has more comparative study data to back its ring-type medical device for blood pressure (BP) called CART BP, which CEO Jack Lee noted has the potential to “replace existing blood pressure monitors.” Sky
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Nelonemdaz

Phase III data positive for GNT's neuroprotective stroke drug

Feb. 14, 2024
By Marian (YoonJee) Chu
South Korean biopharmaceutical firm GNT Pharma Co. Ltd. on Feb. 13 reported positive findings from a domestic phase III trial of its neuroprotectant therapy, nelonemdaz (NEU-2000), for patients with acute ischemic stroke.
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