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BioWorld - Tuesday, February 24, 2026
Home » Topics » Clinical, BioWorld Asia

Clinical, BioWorld Asia
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South Korea's MFDS clears Yuhan trial to continue after investigation into deaths

Aug. 21, 2019
By Jihyun Kim
HONG KONG – Following a regulatory committee's ruling that three of four deaths previously reported during a phase II trial were unrelated to the study drug, South Korea's Ministry of Food and Drug Safety (MFDS) cleared Yuhan Corp. to continue testing lazertinib (YH-25448) in the non-small-cell lung cancer (NSCLC) study.
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Okogen begins phase II trial in Australia with topical ranpirnase to fight adenoviral conjunctivitis

Aug. 14, 2019
By Tamra Sami
PERTH, Australia – San Diego-based Okogen Inc. is taking its clinical trial program to Australia where it will test its lead compound OKG-0301 for acute adenoviral conjunctivitis in the phase II (RUBY) trial.
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I-Mab's antibody cleared for trials in advanced tumors

July 24, 2019
By Elise Mak
HONG KONG – China has approved the fourth homegrown CD47 antibody to start clinical trials, intensifying the local CD47 race. Chinese biologics developer I-Mab Biopharma (Shanghai) Co. Ltd. said it received the go-ahead for the clinical study of TJC-4, its differentiated fully human CD47 monoclonal antibody for treating advanced malignant tumors.
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Bionomics' BNC-210 fails in agitation; hope hangs on PTSD

July 10, 2019
By Tamra Sami
PERTH, Australia – Adelaide, Australia-based Bionomics Inc. reported another trial failure with its lead compound, BNC-210, in elderly patients with agitation, but it is still clinging on to hopes that the compound will show a clinical benefit for post-traumatic stress disorder (PTSD).
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Harbour boosts translational, clinic work via Erasmus pact

July 3, 2019
By Elise Mak
HONG KONG – Shanghai-based biopharma firm Harbour Biomed Therapeutics Ltd. has inked a 10-year pact with Erasmus MC from the University Medical Center Rotterdam to grow its footprint in Europe. Both sides will develop biotherapeutics to treat cancer and immunological diseases.
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Themis’ Chikungunya vaccine heading toward pivotal study after successful phase II trial

Nov. 7, 2018
By Nuala Moran
LONDON – Themis Bioscience GmbH has announced positive phase II results for its vaccine against Chikungunya virus, as it moves to complete an IPO later this week to raise up to €55 million (US$62.6 million) to fund the launch of a pivotal phase III trial.
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