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BioWorld - Friday, December 26, 2025
Home » Topics » Asia-Pacific, BioWorld Asia

Asia-Pacific, BioWorld Asia
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South Korea mulls shift to preferential drug pricing system, but challenges remain

Sep. 14, 2021
By Gina Lee
South Korea’s Ministry of Health and Welfare (MHW) is currently discussing the implementation of a preferential drug pricing system and plans to initiate an expert survey in 2022. The preferential drug pricing system is part of a three-prong strategy that South Korea plans to adopt to promote the growth of eight leading companies in the pharmaceutical, medical device and cosmetic industries by 2030.
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Elderly hands holding broken brain structure

Metabolomics study reveals dementia-linked metabolites

Sep. 14, 2021
By John Fox
A comprehensive nontargeted metabolomics analysis has revealed previously unknown classes of disease-linked metabolites in whole blood samples from dementia patients, which may have significant therapeutic implications for managing the untreatable common cognitive disorder.
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South Korean won

Abion shares drop in South Korean debut, but listing raises $33M for cancer therapies

Sep. 14, 2021
By Gina Lee
Abion Inc., which focuses on precision oncology, raised ₩38.76 billion (US$33.36 million) in its debut on the Korean Stock Exchange’s Kosdaq board on Sept. 8.
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Computer chip over digital background with China flag

China’s new personal information protection law challenges company access to user data

Sep. 14, 2021
By Doris Yu
China’s Personal Information Protection Law (PIPL) will take effect on Nov. 1, 2021, making it harder for tech firms, including health care companies, to access and use consumers’ personal information. The PIPL was officially passed by the National People’s Congress on Aug. 20.
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KRAS protein

Innovent acquires KRAS G12C candidate from Genfleet in $312M deal

Sep. 7, 2021
By Doris Yu
Innovent Biologics Inc. has inked a $312 million licensing deal for the development and commercialization of Genfleet Therapeutics Inc.’s KRAS G12C inhibitor, GFH-925, in mainland China, Hong Kong, Macau and Taiwan. Innovent also has additional option-in rights for global development and commercialization.
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Pill bottle with flag of India

India begins approving long list of banned FDC drugs

Sep. 7, 2021
By T.V. Padma
India’s drug regulator has approved 31 fixed-dose combination (FDC) drugs out of more than 300 banned products, after an assessment by its drugs technical advisory board. It has also asked for more phase IV postmarketing data for 19 others.
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Eyegene-hero-pic-9-7

Eyegene cleared to begin phase I/IIa trial for mRNA COVID-19 vaccine in South Korea

Sep. 7, 2021
By Gina Lee
Eyegene Inc. has received the green light from South Korea’s Ministry of Food and Drug Safety (MFDS) for EG-COVID, its mRNA COVID-19 vaccine, to enter the clinic. Eyegene will now begin a phase I/IIa trial, to be conducted in two stages, to evaluate the vaccine’s safety, tolerability and immunogenicity.
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Jingxin in-licensing epilepsy drug from Bio-Pharm Solutions in $40M deal

Aug. 31, 2021
By Doris Yu
Zhejiang Jingxin Pharmaceutical Co. Ltd. has in-licensed JBPOS-0101, a class I new drug for epilepsy, from Bio-Pharm Solutions Co. Ltd. for mainland China, Hong Kong, and Macau. The partnership could bring South Korea’s Bio-Pharm more than $40 million, including an up-front payment of $5 million, milestone payments of up to $35 million, and potential royalties on future sales.
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Tai-Gyu Kim, CEO, Vigencell

Vigencell debuts on Korean Stock Exchange with $85M raise; shares slide almost 20%

Aug. 31, 2021
By Gina Lee
Vigencell Inc., a company focused on immune cell therapy, raised ₩99.4 (US$85.17 million) through an IPO on South Korea’s Kosdaq board and plans to use the funds to drive its R&D and company operations. “We particularly want to increase the competitiveness of our pipeline by advancing our technology and clinical development,” Vigencell CEO Tai-Gyu Kim told BioWorld. “We will also expand our discovery of new candidates and R&D in general, as well as updating our facilities and hiring researchers.”
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EMA icons

Samsung Bioepis’ Byooviz wins EMA approval

Aug. 31, 2021
By Angie Ling
Samsung Bioepis Co. Ltd. has emerged as the first company to obtain marketing authorization from the EMA for a biosimilar of Lucentis (ranibizumab), a significant development for the Korean biosimilar specialist. The approval comes less than two months after the company received a positive opinion from the EMA’s CHMP for Byooviz (ranibizumab), formerly called SB-11.
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