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BioWorld Asia, Clinical
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Health professional pointing stethoscope at Clinical Trial words, icons

Dragon Boat moves anti-CSF-1R antibody candidate to the clinic

March 23, 2021
By Elise Mak
Like its distinctive name, Dragon Boat Biopharmaceutical Co. Ltd., of Shanghai, raced to victory with the Chinese IND approval for its anti-CSF-1R monoclonal antibody candidate BC-006, marking an important milestone for the company as it embraces a growing focus on innovative medicines.
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Digital eye illustration

Azura Ophthalmics advances to registration study on positive phase II results in Meibomian gland disfunction

March 16, 2021
By Tamra Sami
PERTH, Australia – Sydney-based Azura Ophthalmics Ltd. has moved into a registration trial following positive phase II results for lead candidate AZR-MD-001 in Meibomian gland dysfunction, the leading cause of dry eye disease.
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Kintor’s proxalutamide reduces COVID-19 mortality risk by 92%; trial in ICU patients next

March 16, 2021
By Elise Mak
Kintor Pharmaceutical Ltd. said its androgen receptor (AR) antagonist, proxalutamide, reduced mortality risk by 92% and shortened median hospital length stay by nine days vs. standard of care, based on a preliminary analysis of phase III data from 590 hospitalized COVID-19 patients in Brazil. The company expects to have final data ready by the end of this month or early April, Chief Financial Officer Lucy Lu told BioWorld.
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Target with off-center arrow

Bio-Thera terminates HER2 and Trop2 ADCs and PD-1 inhibitor programs

March 9, 2021
By Elise Mak
In an unusual move for a Chinese company, Bio-Thera Solutions Ltd. terminated the clinical development of its Trop2 antibody-drug conjugate (ADC), BAT-8003, and its PD-1 monoclonal antibody, BAT-1306, a month after it halted the phase III-stage HER2-ADC candidate BAT-8001.
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Ascletis joins Madrigal and Viking in global race for THR-β agonist for NASH

March 2, 2021
By Elise Mak
Liver disease specialist Ascletis Pharma Inc. said its nonalcoholic steatohepatitis (NASH)-focused subsidiary, Gannex Pharma Co. Ltd., will start global development of its oral THR-β agonist, ASC-41, after it obtained an IND approval from the FDA based on positive phase I data generated in China.
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Baby, it’s not as cold inside: Pfizer-Biontech submits new COVID-19 vaccine storage data

Feb. 23, 2021
By Lee Landenberger
Pfizer Inc. and Biontech SE submitted new data to the FDA showing its COVID-19 vaccine’s stability can be maintained at temperatures often found in pharmaceutical freezers and refrigerators: -13°F to 5°F (-25°C to -15°C).
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Health professional pointing stethoscope at Clinical Trial words, icons

Clinical data drops in recent months, but is way ahead of this time last year

Feb. 16, 2021
By Karen Carey
BioWorld tracked a total of 295 phase I, II and III clinical news items in January, a rise of 39% compared with the number recorded during the pre-pandemic month of January 2020.
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Antibodies attacking SARS-CoV-2 virus

Chugai adds to evidence for Actemra’s role in COVID-19 treatment line-up

Feb. 16, 2021
By Gina Lee
HONG KONG – A Japanese phase III study of Chugai Pharmaceutical Co. Ltd.’s interleukin-6 inhibitor Actemra (tocilizumab) in patients hospitalized with severe COVID-19 pneumonia has read out, expanding what’s known about the drug’s use in the pandemic, which had been inconclusive until recently, though is now known to reduce mortality in the vulnerable population.
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Botanix’s cannabidiol eradicates Staphylococcus aureus bacteria in phase IIa nasal colonization study

Feb. 9, 2021
By Tamra Sami
PERTH, Australia – Synthetic cannabinoid company Botanix Pharmaceuticals Ltd. announced top-line data from a phase IIa study showing that two different formulations of BTX-1801, a synthetic cannabidiol (CBD), eradicated Staphylococcus aureus (staph) in the nose, meeting study endpoints for safety and efficacy. 
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Stomach and intestine

GSK discontinues phase II trial of Immutep’s anti-LAG3 immunotherapy in ulcerative colitis

Jan. 26, 2021
By Tamra Sami
PERTH, Australia – Sydney-based Immutep Ltd. announced that Glaxosmithkline plc is discontinuing a phase II ulcerative colitis trial of its anti-lymphocyte activation gene-3 cell-depleting monoclonal antibody, derived from Immutep’s IMP-731 antibody that GSK licensed in 2010.
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