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BioWorld - Wednesday, December 24, 2025
Home » Topics » Coronavirus, BioWorld Asia

Coronavirus, BioWorld Asia
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Japanese shield and coronavirus

Astrazeneca resumes AZD-1222 trials in Japan

Oct. 6, 2020
By Gina Lee
HONG KONG – Cambridge, U.K.-based Astrazeneca plc has resumed phase I/II trials in Japan for AZD-1222, the experimental, adenovirus vector-based candidate coronavirus vaccine that it is co-developing with the University of Oxford.
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Coronavirus vaccine illustration

Spybiotech, Serum Institute of India partner on VLP-based COVID-19 vaccine

Sep. 8, 2020
By Cormac Sheridan
DUBLIN – Spybiotech Ltd. has secured a first vaccine deal for its proprietary Spytag/Spycatcher protein conjugation technology. The Serum Institute of India Pvt. Co. Ltd. (SIIPL) is employing the technology in a COVID-19 virus-like-particle (VLP)-based vaccine, which recently entered a phase I/II trial in Australia. An initial data readout is expected in October or November.
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Antibodies fighting coronavirus

Celltrion doubles pace for COVID-19 antibody treatment CT-P59

Aug. 4, 2020
By Gina Lee
HONG KONG – Incheon, South Korea-based Celltrion Inc. is rapidly advancing CT-P59, its antiviral antibody treatment for the COVID-19 virus, after receiving its second green light to begin phase I trials.
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RNA and SARS-CoV-2 virus cell

Olix close to bringing COVID-19 drug candidate to the clinic

July 31, 2020
By Gina Lee
HONG KONG – Suwon-based Olix Pharmaceuticals Inc. is completing the final preclinical work before starting clinical trials for its as-yet-unnamed COVID-19 drug candidate, developed inside three months using RNA interference (RNAi) technology.
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Glenmark’s phase III favipiravir study finds drug speeds clinical improvement for some patients

July 28, 2020
By David Ho
HONG KONG – Mumbai, India-headquartered Glenmark Pharmaceuticals Ltd. have released statistically significant top-line results from a phase III trial showing that Fabiflu (favipiravir), an antiviral pyrazine RNA polymerase inhibitor, can treat cases of mild to moderate COVID-19 in four days.
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Coronavirus vaccine/therapeutics illustration

China’s Kintor to provide AR antagonist for COVID-19 trial in Brazil

July 14, 2020
By Elise Mak
BEIJING – Androgen receptor (AR) antagonist developer Kintor Pharmaceutical Ltd., of Suzhou, China, is going to provide its proxalutamide (GT-0918) to an ongoing clinical trial in male patients, led by U.S. firm Applied Biology Inc., in Brazil for COVID-19, after preliminary clinical research suggested a potential link between androgenetic alopecia and COVID-19 pathogenesis.
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India’s first COVID-19 vaccine to enter human trials

July 7, 2020
By David Ho and Bryan Wong
Bharat Biotech International Ltd. has successfully developed India’s first indigenous vaccine candidate for COVID-19 to enter human trials. Named Covaxin, the vaccine has been cleared by the Drug Controller General of India (DCGI) and Ministry of Health & Family Welfare for phase I and II trials after the company submitted positive preclinical study results regarding safety and immune response.
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Disintegrating coronavirus

Snowballing research preps avalanche to bury COVID-19

July 7, 2020
By Karen Carey
Research focused on finding viable solutions to counter the COVID-19 pandemic continues at an explosive pace with a total of 588 potential therapeutics and vaccines at the forefront of scientific efforts launched by industry, academia and government.
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Empty waiting room

Poised for second round, pandemic creates backlog of untreated diseases

June 23, 2020
By Mari Serebrov
Countries and health care providers should hope for the best but prepare for the worst as a resurgence of COVID-19 is expected in the fall, just as the influenza season hits.
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Man wearing mask, receiving coronavirus vaccine

CNBG reports 100% seroconversion rate for COVID-19 vaccine candidate

June 23, 2020
By Elise Mak
BEIJING – Chinese state-backed vaccine developer China National Biotec Group (CNBG), of Beijing, said on June 16 that its inactivated COVID-19 vaccine candidate produced a seroconversion rate of up to 100% in a phase I/II trial that enrolled 1,120 healthy subjects.
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