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BioWorld - Saturday, July 4, 2026
Home » Topics » Asia-Pacific, BioWorld

Asia-Pacific, BioWorld
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S. Korea must ease regs, fast-track tech solutions to spur cell, gene therapy R&D

Sep. 3, 2019
By Jihyun Kim
SEOUL – South Korea's investors have become very interested in the global cell and gene therapy market. Licensing and M&A deals in the field have been active – a good sign for Korean biopharma firms eager to tap in.
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Long-term growth hit by short-term troubles

Sep. 3, 2019
By Jihyun Kim
SEOUL – After a decade of steady increases, venture capital (VC) investments in South Korea's biotech sector are more active. But for the country's strategic financial plan to be sustainable, it will have to further strengthen its science capabilities, according to experts at the Korea Bio Investment Conference (KBIC) last week in Seoul.
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Elixiron secures $10.5M, eyes first and best-in-class immunotherapies

July 31, 2019
By Elise Mak
TAIPEI, Taiwan – Budding Taiwanese startup Elixiron Immunotherapeutics Inc. closed a $10.5 million series A1 financing to further expand its technology platform and drive its drug candidates toward clinical development.
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Biopharma investments set to drop in 2019, but deal flow to stay strong: experts

July 29, 2019
By Elise Mak
TAIPEI, Taiwan – Asian capital continues to play a key role in funding biotech development regionally and globally through private investments, M&A deals or IPOs. And 2018 was a particularly exciting one for cross-border investments and health care IPOs, said speakers at the BIO Asia conference. The total deal value of global biopharma IPOs and M&A deals hit a record $49 billion in 2018.
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Trade dispute: South Korea's pharma industry to be affected by Japan's plan on 'White List'

July 25, 2019
By Jihyun Kim
HONG KONG – The trade feud between South Korea and Japan has worsened since the beginning of July, when the Japanese government said it would impose new regulations on exports to Korea. The new policies are mostly applied to elements of semiconductor technology but also includes some pharmaceutical components and devices, leading to concerns that the regulations will affect Korea's pharmaceutical sector.
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Despite volatile market so far, HKEX still drawing biotechs as Sinomab applies for IPO

July 23, 2019
By Alex Ho
HONG KONG – Sinomab Bioscience Ltd., a Hong Kong clinical-stage antibody firm, said its application for a Hong Kong IPO was accepted by the stock exchange, making it the 16th biopharma to submit an application under the new rules of the Hong Kong Exchange (HKEX).
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Biocure's South Korean unit advancing CAR T programs with private placement funds

July 18, 2019
By Jihyun Kim
HONG KONG – Biocure Technology Corp., a Canadian biopharmaceutical company focusing on biosimilar products, is advancing a CAR T product through its South Korean subsidiary, Biocurepharm Inc., thanks to a recently closed private placement.
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Industry supports most TGA proposals for CDx regs but seeks clarity

July 16, 2019
By Tamra Sami
PERTH, Australia – The majority of comments were positive for the Therapeutics Goods Administration's proposal for regulating in vitro companion diagnostics (IVD CDx) to ensure the devices receive appropriate premarket scrutiny.
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Singapore's Prestige to sell Herceptin biosimilar in Europe through Mundipharma deal

July 15, 2019
By Jihyun Kim
HONG KONG – Prestige Biopharma Pte. Ltd., a Singapore-headquartered pharmaceutical company under the Prestige Group, has agreed to grant exclusive license to U.K.-based multinational company Mundipharma International Ltd. for distribution and sale of its trastuzumab biosimilar, Tuznue, in western European markets, including France, Spain, Norway, Sweden, Denmark, Finland, Portugal, Switzerland and Austria.
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TGA receives mixed response from industry on proposal to begin formal GCP inspections

July 11, 2019
By Tamra Sami
PERTH, Australia – Australia's Therapeutic Goods Administration (TGA) received mixed comments from stakeholders on whether it was necessary to implement a formal good clinical practices inspections program in Australia. Many comments questioned how inspectional findings from a proposed pilot program would be released, but most agreed that a formal inspections program would raise compliance and enhance international competitiveness.
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