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BioWorld - Thursday, January 29, 2026
Home » Topics » Regions » Asia-Pacific

Asia-Pacific
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Ear illustration

FDA gives thumbs up to Cochlear’s implantable bone conduction hearing system

Dec. 3, 2019
By Tamra Sami
The U.S. FDA has cleared Cochlear Ltd.’s newest cochlear implant, the Osia 2 system, an active implantable bone conduction hearing system. Unlike Cochlear’s traditional implant, the Osia implant bypasses damaged parts of the ear and sends sound vibrations directly to the cochlea.
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In India, government steps up efforts to develop more TB testing and treatment

Dec. 3, 2019
By T.V. Padma
HYDERABAD, India – India, home to a quarter of the global tuberculosis (TB) cases, plans to enhance its capacity to fight TB drug resistance and bolster susceptibility testing under a new initiative launched by the Geneva-based nonprofit Foundation for Innovative New Diagnostics (FIND).
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Flag of India

Indian pharma sector needs to learn from its competitors: report

Dec. 3, 2019
By T.V. Padma
NEW DELHI, India - While India is still an attractive prospect for investment in biotechnology, with plenty of potential waiting to be tapped by investors, the country needs to learn from the successful examples of other countries, including its Asian biotech competitors, according to a new report.
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Alteogen licenses ALT-B4 to a top 10 global pharma in potential $1B+ deal

Dec. 3, 2019
By Jihyun Kim
HONG KONG – South Korean company Alteogen Inc. signed a nonexclusive global license agreement with a top 10 global pharmaceutical company for its recombinant human hyaluronidase enzyme, ALT-B4, in exchange for an up-front payment of $13 million.
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Celltrion’s Remsima SC wins marketing approval in EU

Nov. 27, 2019
By Jihyun Kim
HONG KONG – Celltrion Healthcare Co. Ltd., a South Korean biopharmaceutical corporation, won European Union (EU) marketing approval for Remsima SC for the treatment of rheumatoid arthritis (RA), as a subcutaneous version of Celltrion’s infliximab biosimilar, CT-P13.
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Stem cells

Australian researchers create kidney tissue from iPS cells

Nov. 26, 2019
By Tamra Sami
MELBOURNE, Australia – Researchers at the Murdoch Children’s Research Institute in Melbourne are pushing the boundaries on creating kidney tissue from stem cells. For more than two decades, Melissa Little and her team at Murdoch have investigated the molecular and cell development basis of kidney disease and the potential for regeneration. The team has developed approaches for directing the differentiation of human pluripotent stem cells to human kidney organoids and is applying that knowledge to disease modeling, drug screening, cell therapy and tissue engineering.
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ESMO Asia Congress 2019

Moving West to East: Panelists focus on Asia-prevalent cancers, NGS tests and precision oncology

Nov. 26, 2019
By David Ho
SINGAPORE – As the ESMO Asia Congress 2019 brought 3,679 participants from all over the Asia-Pacific region and beyond to Singapore’s Suntec Convention & Exhibition Centre, the focus, unsurprisingly, was on developments and challenges relevant to the oncology community.
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Coins and seedling

Lucence attracts $20M in series A to scale up operations

Nov. 26, 2019
By Jihyun Kim
HONG KONG – Lucence Diagnostics Pte Ltd., a genomic medicine company headquartered in Singapore, has secured $20 million in series A investment.
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ESMO Asia 2019

Panelists urge better designs, more global focus for phase I trials

Nov. 25, 2019
By David Ho
SINGAPORE – While a lot of focus is placed on phase III trials and the subsequent approvals, panelists during the ESMO Asia Congress pointed to the importance of designing the right kind of phase I trials, from reaching global populations to using appropriate endpoints.
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ESMO Asia 2019

Quality of life and quality of studies take stage as Takeda reports solid NSCLC findings

Nov. 25, 2019
By David Ho
SINGAPORE – Takeda Pharmaceutical Co. Ltd. presented new findings from its phase III ALTA-1L trial evaluating its Alunbrig (brigatinib) vs. crizotinib in adults with advanced anaplastic lymphoma kinase-positive (ALK+) non-small-cell lung cancer (NSCLC) who had not received a prior ALK inhibitor, showing Alunbrig reduced the risk of disease progression or death by 76% after more than two years of follow-up.
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