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BioWorld - Thursday, April 30, 2026
Breaking News: Read BioWorld's AACR 2026 coverageBreaking News: Best of BioWorld: Q1
Home » Topics » BioWorld Asia, Clinical

BioWorld Asia, Clinical
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No sweat: Brickell’s anticholinergic data paves the way to Asia

June 16, 2020
By Lee Landenberger
All the primary and secondary efficacy endpoints were met in Boulder, Colo.-based Brickell Biotech Inc.’s pivotal phase III study of the anticholinergic sofpironium bromide in treating primary axillary hyperhidrosis, which involves excessive sweating in the armpits that interferes with daily life and work.
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Coronavac product packaging

Sinovac unveils positive results for COVID-19 vaccine candidate, aims to start phase III next month

June 16, 2020
By Elise Mak
BEIJING – Nasdaq-listed Chinese vaccine developer Sinovac Biotech Ltd., of Beijing, said the preliminary results of the phase I/II trials of its COVID-19 inactivated vaccine candidate, Coronavac, demonstrated favorable immunogenicity and safety profiles.
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Seikagaku, Ono Pharma plan next steps for arthritis drug after positive Japan phase III results

June 16, 2020
By Gina Lee
HONG KONG – Japan’s Seikagaku Corp. is contemplating the next move for its ONO-5704/SI-613 (diclofenac etalhyaluronate), a treatment for arthritis that it is co-developing with fellow Japanese company Ono Pharmaceutical Co. Ltd.
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Lungs

Dimerix’s lead candidate to enter global REMAP-CAP trial to treat COVID-19 ARDS

June 9, 2020
By Tamra Sami
PERTH, Australia – Melbourne, Australia-based Dimerix Ltd. saw its shares gain 66% on the news that its lead candidate, DMX-200, has been chosen to enter the global REMAP-CAP platform trial as a potential treatment  for COVID-19-related acute respiratory distress syndrome (ARDS).
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Qurient to start phase I trials for triple kinase inhibitor Q-702

June 2, 2020
By Gina Lee
HONG KONG – South Korea’s Qurient Co. Ltd., located in Gyeonggi-do, is preparing to send its novel drug, Q-702, into the clinic after receiving clearance from the U.S. FDA.
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Antibody

Optimistic Sorrento looking to have COVID-19 antibody ready by October

June 2, 2020
By Elise Mak and Alfred Romann
With some positive early data for an antibody to block the COVID-19 virus, Sorrento Therapeutics Inc. is now looking to test a product in a few dozen intensive care patients by the end of July or early August and move into a much broader pool of patients by October.
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China’s Carsgen set to start trials for first claudin18.2-targeted CAR T-cell therapy

May 26, 2020
By Elise Mak
BEIJING – CAR T-cell therapeutics developer Carsgen Therapeutics Co. Ltd., of Shanghai, won IND clearance from the FDA for its first-in-class CT-041 for advanced gastric and pancreatic cancers. The company said it is the first claudin18.2 (CLDN18.2)-targeted CAR T-cell therapy cleared for clinical trials in the world.
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Health professional pointing stethoscope at Clinical Trial words, icons

Luoxin’s PIK3α inhibitor receives trial nod in China after Novartis’ alpelisib

May 19, 2020
By Elise Mak
BEIJING – Shandong, China-based Luoxin Pharmaceuticals Group Stock Co. Ltd. said its PIK3α inhibitor, LX-086, has been approved by China’s National Medical Products Administration (NMPA) to enter clinical trials for advanced solid tumors.
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Lungs, COVID-19 test tube, health care worker in PPE

Proteona to use single-cell proteogenomics platform for Australian COVID-19 vaccine trial

May 12, 2020
By David Ho
HONG KONG – Singapore-based Proteona Pte. Ltd. has started a partnership to characterize the clinical response to a new COVID-19 vaccine, with clinical trials soon to start at Flinders Medical Centre testing the candidate developed in collaboration with Adelaide, Australia-based Vaxine Pty Ltd.
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Patient given oral swab

Support for human challenge trials gaining traction to accelerate COVID-19 vaccine work

May 12, 2020
By Nuala Moran
LONDON – Support is growing for human challenge trials in COVID-19 to be approved in order to speed up development of effective vaccines against the pandemic infection. The World Health Organization (WHO) has just released guidelines for assessing the ethical acceptability, saying such trials would allow for more rapid and standardized testing, accelerating development and enabling candidates to be prioritized.
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