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Home » Topics » BioWorld Asia, Regulatory

BioWorld Asia, Regulatory
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Leqembi

Could Eisai’s Leqembi approval be the trigger for drug price reform in Japan?

Oct. 3, 2023
By Tamra Sami
As pricing negotiations for Biogen Inc./Eisai Co. Ltd.’s newly approved Leqembi (lecanemab) for Alzheimer’s disease get underway at Japan’s Central Social Insurance Medical Council (Chuikyo), industry watchers see opportunity for potential drug price reform.
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Samsung Biologics Bio Campus II

Samsung, Celltrion set record targets as S. Korea banks on Bio Economy 2.0

Oct. 3, 2023
By Marian (YoonJee) Chu
As South Korea increases its stakes on the “bioeconomy” as its next growth engine and as its “second semiconductor industry,” leading domestic biologic and biosimilar drug producers such as Samsung Biologics Co. Ltd. and Celltrion Inc. are setting record production targets to become forerunners in the global playing field.
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Cyclopharm Technegas

FDA approves Cyclopharm’s Technegas combo product for visualizing pulmonary ventilation

Oct. 2, 2023
By Tamra Sami

After a long and bumpy path to approval, the U.S. FDA has finally given the green light to Cyclopharm Ltd’s Technegas combination product a day after the Sept. 29 PDUFA date.


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Cyclopharm Technegas

FDA approves Cyclopharm’s Technegas combo product for visualizing pulmonary ventilation

Oct. 2, 2023
By Tamra Sami
After a long and bumpy path to approval, the U.S. FDA has finally given the green light to Cyclopharm Ltd’s Technegas combination product a day after the Sept. 29 PDUFA date.
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US-South Korean flags

Korean biosimilars locked in ‘fierce’ battle to box out competition in US

Sep. 29, 2023
By Marian (YoonJee) Chu
National support for the biosimilar sector and the domestic industry’s efforts to increase production and sales may not be enough for South Korean biosimilar firms to box out competition in the ever-changing regulatory court of the U.S.
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Lee Chang-yang, minister, MOTIE

South Korea rolls out ‘Bio Economy 2.0’ to top global biologics, biosimilar market

Sep. 27, 2023
By Marian (YoonJee) Chu
In July 2023, South Korea’s Ministry of Trade, Industry and Energy ramped up efforts to kickstart the so-called “Bio Economy 2.0,” the newfound initiative that banks on the biopharmaceutical industry to potentially revitalize the country’s slowing economic and social growth. Highlighting four major areas – biopharmaceuticals, biomaterials, bioenergy and digital technologies – as the four “wheels” to carry the biopharma industry, the new plan underscored the government’s unwavering support for the sector while highlighting its vision to become the “number one bioeconomy” worldwide.
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Japan’s MHLW approves slew of new drugs, including Eisai/Biogen’s Leqembi for Alzheimer’s

Sep. 26, 2023
By Tamra Sami
Thanks to a raft of new approvals by Japan’s Ministry of Health, Labor and Welfare (MHLW), patients in Japan will soon have access to Biogen Inc./Eisai Co. Ltd.’s Leqembi (lecanemab), an amyloid-beta binder, for slowing progression of mild cognitive impairment and mild dementia due to Alzheimer's disease.
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Innovent scores first approval for PCSK9 inhibitor in China

Aug. 22, 2023
By Tamra Sami
China’s National Medical Products Administration has approved Innovent Biologics Inc.’s proprotein convertase subtilisin/kexin-type 9 (PCSK9) inhibitor, Sintbilo (tafolecimab), making it the first first locally developed PCSK9 monoclonal antibody to be approved in China.
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Multiple myeloma illustration

Oricell clears IND hurdle for homegrown CAR T in China

Aug. 15, 2023
By Marian (YoonJee) Chu
Oricell Therapeutics Co. Ltd. has become the latest Chinese biotech to advance an independently developed CAR T therapy, announcing Aug. 10 that China’s regulatory body gave IND approval for Oricar-017. Oricar-017 is the Shanghai-based biotech’s GPRC5D-directed CAR T therapy developed to treat patients with relapsed or refractory multiple myeloma.
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Rx quality problems continue to aggravate supply issues

Aug. 8, 2023
By Mari Serebrov
In a balancing act between supply and drug quality, the U.S. FDA tipped the scales on behalf of quality, slapping an import alert on Intas Pharmaceuticals Ltd. in June, followed by a July 28 warning letter requiring the India-based company to develop and implement a global corrective action and preventive action plan.
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