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BioWorld - Thursday, May 19, 2022
Home » Topics » Asia-Pacific » China

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China’s Harbour Biomed out-licenses preclinical bispecific antibody to Astrazeneca for $350M

April 12, 2022
By Tamra Sami
No Comments
Harbour Biomed Therapeutics Ltd. has out-licensed a preclinical bispecific antibody, HBM-7022, to Astrazeneca plc in a global licensing deal worth up to $350 million.
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Clinical research concept with medical icons on light bulb

Ark Bio shares positive data for first positive RSV antiviral phase III

April 12, 2022
By David Ho
No Comments
Ark Biopharmaceutical Co. Ltd.’s phase III testing its ziresovir in infants hospitalized with respiratory syncytial virus (RSV) infection produced positive top-line results, meeting both the primary endpoint of reduction in signs and symptoms (S&S) score (p=0.002) and a key secondary endpoint of reduction in viral load (p=0.006) compared with placebo. The company said it is the first oral RSV antiviral to be successful in phase III.
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Allist's furmonertinib meets primary endpoint in phase III trial to treat lung cancer

April 12, 2022
By Doris Yu
No Comments
Shanghai Allist Pharmaceuticals Co. Ltd.’s third-generation EGFR tyrosine kinase inhibitor, furmonertinib, met its primary endpoint in a phase III trial, demonstrating longer progression-free survival vs. first-generation EGFR TKI Iressa (gefitinib, Astrazeneca plc) as first-line therapy for locally advanced or metastatic EGFR mutation-positive non-small-cell lung cancer.
Read More
Person wearing mask, glove holding pill

Phase III proxalutamide opens door for Kintor in COVID-19

April 12, 2022
By Randy Osborne
No Comments
Shares of Suzhou, China-based Kintor Pharmaceutical Ltd. (HKEX:9939) rose to HKD28.85 (US$3.68), up HKD14.87, or 106%, after the firm reported top-line data from the phase III multiregional trial with proxalutamide in people with mild to moderate COVID-19 infection, regardless of vaccination status or risk factors.
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CAR T cell attacking cancer cells

Cellpoint acquires US, European rights to Pregene CAR T therapy in €20M+ deal

April 12, 2022
By Doris Yu
No Comments
Cellpoint B.V. has picked up U.S and European rights to a chimeric antigen receptor T-cell (CAR T) therapy from Shenzhen Pregene Biopharma Co. Ltd. Cellpoint will develop and commercialize the candidate, PRG-1801, for the treatment of hematological indications.
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Female health professional holding Truscreen device

Truscreen’s AI cervical cancer screening tool showing promise for primary screening

April 8, 2022
By Tamra Sami
No Comments
Truscreen Group Ltd. completed its largest clinical trial to date that showed its cervical cancer screening device surpassed liquid-based cytology (LBC) screening in 15,651 women across 64 hospitals in nine provinces in China over three years.
Read More
Deal illustration

China’s Harbour Biomed out-licenses preclinical bispecific antibody to Astrazeneca for $350M

April 8, 2022
By Tamra Sami
No Comments
Harbour Biomed Therapeutics Ltd. has out-licensed a preclinical bispecific antibody, HBM-7022, to Astrazeneca plc in a global licensing deal worth up to $350 million.
Read More
Cancer cells under magnifying glass

Researchers in China find evidence in mice that bacteria in tumors help cancer cells metastasize

April 8, 2022
By Tamra Sami
No Comments
Researchers in China have discovered that bacteria promote cancer metastasis by bolstering the strength of host cells against mechanical stress in the bloodstream, promoting cell survival during tumor progression.
Read More
Person wearing mask, glove holding pill

Phase III proxalutamide opens door for Kintor in COVID-19

April 6, 2022
By Randy Osborne
No Comments
Shares of Suzhou, China-based Kintor Pharmaceutical Ltd. (HKEX:9939) rose to HKD28.85 (US$3.68), up HKD14.87, or 106%, after the firm reported top-line data from the phase III multiregional trial with proxalutamide in people with mild to moderate COVID-19 infection, regardless of vaccination status or risk factors.
Read More

Allist's furmonertinib meets primary endpoint in phase III trial to treat lung cancer

April 6, 2022
By Doris Yu
No Comments
Shanghai Allist Pharmaceuticals Co. Ltd.’s third-generation EGFR tyrosine kinase inhibitor, furmonertinib, met its primary endpoint in a phase III trial, demonstrating longer progression-free survival vs. first-generation EGFR TKI Iressa (gefitinib, Astrazeneca plc) as first-line therapy for locally advanced or metastatic EGFR mutation-positive non-small-cell lung cancer.
Read More
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