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BioWorld - Sunday, February 15, 2026
Home » Topics » Japan, BioWorld Asia

Japan, BioWorld Asia
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Japanese shield and coronavirus

Japan advances fight against COVID-19 with four-day approval for remdesivir

May 12, 2020
By David Ho and Gina Lee
HONG KONG – Japan has become the first country in the world to approve Veklury (remdesivir), Gilead Sciences Inc.’s experimental drug, to treat COVID-19. The fast approval was based on U.S. data and that country’s emergency use of the drug to tackle the pandemic, although it is unclear whether the drug is safe or effective for treating COVID-19.
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Fujifilm stock rises as Japan considers Avigan for COVID-19 treatment

Feb. 25, 2020
By Jihyun Kim
HONG KONG – Fujifilm Holdings Corp. stock (TYO:4901) jumped 8.8% to ¥5,890 (US$53.48) on Feb. 25, as Japan considers using Avigan (favipiravir), an anti-influenza medication developed by the company’s Toyama Chemical Co. Ltd., to treat COVID-19. The share price ended the day at ¥5,567, for a gain of 2.83%.
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Japan flag doctor

Japan’s drug repricing plan to hit some top sellers

Feb. 4, 2020
By Jihyun Kim
HONG KONG – Aiming to increase the financial stability of the national health care insurance system, Japan has announced a list of 17 drugs for which prices will be reduced. The country’s Central Social Insurance Medical Council, an advisory group from the Ministry of Health, Labour and Welfare (MHLW), approved the drug repricing system on Jan. 22.
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HTA and drug/device pricing in Asia in 2020

Dec. 31, 2019
By David Ho
MALAYSIA – Asian countries, like India, have been struggling to find a middle ground to the effective pricing of drugs and medical devices over the past year and several are looking at health technology assessment (HTA) programs as a solution for this issue.
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Shionogi bogey at adcom cefiderocol's death hitch; cUTI drug voted Credible

Oct. 23, 2019
By Randy Osborne
The FDA's Antimicrobial Drugs Advisory Committee last week backed by a large margin cefiderocol for treatment of complicated urinary tract infections (cUTIs), despite the mortality disparity found by Shionogi & Co. Ltd. among critically ill drug-treated patients in the descriptive phase III trial in severe infections called Credible-CR.
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Chong Kun Dang receives Japan's approval for NESP biosimilar to treat anemia

Oct. 9, 2019
By Jihyun Kim
HONG KONG – South Korea's Chong Kun Dang (CKD) Pharmaceutical Corp. received approval for its novel erythropoiesis stimulating protein (NESP) biosimilar from Japan's Ministry of Health, Labour and Welfare (MHLW). The drug (CKD-1110) is world's first NESP biosimilar to treat anemia.
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Sumitomo Dainippon strikes rich tie-up with Roivant; shells out $3B for ownership in five 'Vants'

Sep. 11, 2019
By Michael Fitzhugh
Japan's Sumitomo Dainippon Pharma Co. Ltd. plans to pay $3 billion to acquire Roivant Sciences Ltd.'s ownership interests in five biopharma companies, plus options to acquire up to six more from the prolific company-builder. The deal, slated to close in October, would give Sumitomo Dainippon controlling interests in Myovant Sciences Inc., Urovant Sciences Inc., Enzyvant Therapeutics Inc. and Altavant Sciences Inc., as well as an equity stake of more than 10% in Roivant itself.
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