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BioWorld - Saturday, May 30, 2026
Home » Topics » Asia-Pacific » Australia

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Globe showing Asia-Pacific region
Year in review

AI drives financings, approvals for APAC med-tech in 2024

Dec. 27, 2024
By Marian (YoonJee) Chu
AI pulled in major financings and approvals for Asia med-techs in 2024 as Asia Pacific countries played to individual strengths to maximize AI’s applications in the health care sector. While breakaway AI technologies like OpenAI’s ChatGPT reshaped and boosted many industries, AI also drove major financings for APAC med-techs weathering a wider macroeconomic downturn, with AI-based companies accounting for five out of 11 IPOs tracked on BioWorld’s med-tech IPOs list.
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Antibodies attacking cancer cell
Immuno-oncology

Cstone files to start human studies of PD-1/VEGF/CTLA-4 antibody

Dec. 23, 2024
Cstone Pharmaceuticals Co. Ltd. has filed a clinical trial application in Australia seeking to initiate a first-in-human study of CS-2009 for solid tumors. The company plans to initiate a multi-regional trial for CS-2009 in Australia early next year, followed by expansion into China and the U.S.
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Monoclonal antibody illustration
Cancer

177Lu-RAD-202 approved for therapeutic phase I in Australia

Dec. 23, 2024
Radiopharm Theranostics Ltd. has been granted Belberry Human Research Ethics Committee (HREC) approval in Australia to initiate a first-in-human phase I therapeutic study of 177Lu-labeled RAD-202 (177Lu-RAD-202) for the treatment of HER2-expressing solid tumors, including breast and gastric cancers.
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SK Bioscience scientist in lab

SK Bioscience to start mRNA vax trial for Japanese encephalitis

Dec. 17, 2024
By Marian (YoonJee) Chu
SK Bioscience Co. Ltd. gained approval from the Human Research Ethics Committee in Australia to start phase I/II trials of GBP-560, its mRNA-based vaccine candidate for mosquito-borne Japanese encephalitis virus, with funding from Coalition for Epidemic Preparedness Innovations.
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Synthetic antibiotic Recce-327

Recce moves to pivotal trials in Indonesia for diabetic foot ulcers

Dec. 17, 2024
By Tamra Sami
Recce Pharmaceuticals Ltd. is progressing synthetic antibiotic Recce-327 to pivotal phase III trials in Indonesia for the treatment of diabetic foot infections. The trial, which is assessing Recce-327 as a topical gel (R327G), is expected to begin in the first quarter of 2025, Recce CEO James Graham told BioWorld.
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Synthetic antibiotic Recce-327

Recce moves to pivotal trials in Indonesia for diabetic foot ulcers

Dec. 16, 2024
By Tamra Sami
Recce Pharmaceuticals Ltd. is progressing synthetic antibiotic Recce-327 to pivotal phase III trials in Indonesia for the treatment of diabetic foot infections. The trial, which is assessing Recce-327 as a topical gel (R327G), is expected to begin in the first quarter of 2025, Recce CEO James Graham told BioWorld.
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Immune

SK Bioscience’s mRNA Japanese encephalitis vaccine receives clinical trial clearance in Australia

Dec. 13, 2024
SK Bioscience has received approval from the Human Research Ethics Committee in Australia for a phase I/II trial of its mRNA-based Japanese encephalitis vaccine candidate, GBP-560.
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SK Bioscience scientist in lab

SK Bioscience to start mRNA vax trial for Japanese encephalitis

Dec. 12, 2024
By Marian (YoonJee) Chu
SK Bioscience Co. Ltd. gained approval from the Human Research Ethics Committee in Australia to start phase I/II trials of GBP-560, its mRNA-based vaccine candidate for mosquito-borne Japanese encephalitis virus, with funding from Coalition for Epidemic Preparedness Innovations.
Read More

Paradigm's AU$16M moves Zilosul to pivotal osteoarthritis trials

Dec. 10, 2024
By Tamra Sami
Paradigm Biopharmaceuticals Ltd. raised AU$16 million (US$10.31 million) in a placement that will allow the company to start a global phase III trial with its lead product, Zilosul (injectable pentosan polysulfate/iPPS), to treat osteoarthritis.
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Bionomics progresses BNC-210 to phase III in PTSD

Dec. 10, 2024
By Tamra Sami
Bionomics is progressing BNC-210 to phase III trials in post-traumatic stress disorder (PTSD) following positive feedback from the U.S. FDA. Final data from the phase II Attune study showed that BNC-210 improved PTSD symptom severity at week 12 with efficacy observed as early as week four.
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