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BioWorld - Thursday, July 2, 2026
Breaking News: Science fiction realized: BCI tech is hereBreaking News: Science fiction realized: BCI tech is here
Home » Topics » BioWorld Asia, Clinical

BioWorld Asia, Clinical
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Celltrion advancing COVID-19 antibody treatment CT-P59 and trials continue

Sep. 15, 2020
By Gina Lee
HONG KONG – Interim results of a phase I study CT-P59, an anti-COVID-19 monoclonal antibody being developed by Incheon, South Korea-based Celltrion Inc., have confirmed the candidate’s safety, tolerability and pharmacokinetics in healthy subjects, giving the company confidence to ramp up production of the experimental antiviral.
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Hanmi considers options with diabetes candidate efpeglenatide back in-house

Sep. 15, 2020
By David Ho and Gina Lee
HONG KONG – Sanofi SA has finally ended its clinical development of Hanmi Pharmaceutical Co. Ltd.’s efpeglenatide as a type 2 diabetes treatment, and the Korean firm is now considering how to move forward with developing the once-weekly GLP-1 receptor agonist, which employs Hanmi's Lapscovery delivery technology.
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Sputnik V COVID-19 vaccine vials

Early clinical data illuminate Russia’s Sputnik V COVID-19 vaccine

Sep. 8, 2020
By Nuala Moran
LONDON – Results from two non-randomized phase I/II trials of the Russian COVID-19 vaccine Sputnik V that recently received conditional regulatory approval show both a frozen and a freeze-dried formulation of the two-shot vaccine had a good safety profile and induced antibody responses in all 76 participants within 21 days.
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Tessa enjoys positive results from two phase I/II trials of CD30 CAR T-cell therapy

Aug. 18, 2020
By David Ho
HONG KONG – Singapore-based Tessa Therapeutics Pte. Ltd. released the results of two investigator-initiated phase I/II trials that found its autologous CD30 CAR T-cell therapy TT-11 showed a high rate of durable complete responses and a favorable safety profile in patients with relapsed/refractory Hodgkin lymphoma.
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Coronavirus microscopic model

CNBG unveils interim data of inactivated vaccine candidate for COVID-19

Aug. 18, 2020
By Elise Mak
Chinese state-backed vaccine developer China National Biotec Group (CNBG), of Beijing, published an interim analysis of randomized phase I/II trials of its inactivated SARS-CoV-2 vaccine candidate in the Journal of the American Medical Association last week. With the added detail, the data encouraged the company in its plans to produce 220 million doses per year.
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Jiangsu Hengrui gets Korea’s green light to pursue drug combo in phase III HCC trial

Aug. 18, 2020
By Gina Lee
HONG KONG – China’s Lianyungang-based Jiangsu Hengrui Medicine Co. Ltd. has obtained approval from Korea’s Ministry of Food and Drug Safety (MFDS) to begin a phase III trial for a combination therapy of its PD-1 inhibitor candidate camrelizumab and VEGFR-2 inhibitor rivoceranib.
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Health professional reading lung scan

Ono teases positive results for Opdivo and bevacizumab combo study

Aug. 11, 2020
By Gina Lee
HONG KONG – Osaka, Japan-based Ono Pharmaceutical Co. Ltd. has obtained positive top-line data in its phase III study of a combination of Opdivo (nivolumab, Bristol Myers Squibb Co.) and bevacizumab in lung cancer patients.
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Taiwan’s Senhwa advancing CK2 candidate against moderate COVID-19

Aug. 4, 2020
By Elise Mak
Senhwa Biosciences Inc., of Taipei, Taiwan, said casein kinase 2 (CK2) is the right target to aim at when developing a COVID-19 therapeutic treatment. The company’s silmitasertib is the only clinical-stage inhibitor of CK2, a kinase recently identified by researchers as being hijacked by SARS-CoV-2.
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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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