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BioWorld - Saturday, March 7, 2026
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Home » Topics » BioWorld Asia, Australia

BioWorld Asia, Australia
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Year in review 2024 - Asia deals and innovation

Japan deals big, wins approvals, mulls CGT; Korea, Australia, too

Dec. 31, 2024
By Tamra Sami and Marian (YoonJee) Chu
At Bio Japan 2024, policymakers and industry leaders pledged to make Japan a land of drug discovery to attract native and foreign drug developers. Like many Asian countries, Japan is harnessing and prioritizing the bio sector to drive economic growth, throwing its weight behind its 10-year Bioeconomy initiative to create bioclusters and increase investment.
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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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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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Rendering of iNKT cell

Arovella heads toward clinic with CAR-19-iNKT cells

Dec. 3, 2024
By Tamra Sami
Arovella Therapeutics Ltd. is heading toward the clinic with its lead product, ALA-101, which consists of a chimeric antigen receptor (CAR) targeting CD19 and invariant natural killer T (iNKT) cells.
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Bladder cancer illustration

Radiopharma Telix acquires FAP-targeting agents for bladder cancer

Nov. 26, 2024
By Tamra Sami
Radiopharmaceutical company Telix Pharmaceuticals Ltd. has inked a deal worth up to AU$264 million (US$171 million) to license and develop next-generation radiopharma imaging and therapy technology targeting fibroblast activation proteins found in a wide range of cancers.
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Frank Borriello, CEO, Alloplex
Newco news

Alloplex’s Suplexa reawakens immune cells to fight cancer

Nov. 26, 2024
By Tamra Sami
When it comes to cell therapy, Alloplex Biotherapeutics Inc. CEO Frank Borriello said he believes that autologous, personalized therapy is the only thing that makes sense. “The allure of an off-the-shelf therapy has been such a magnet. It sucked in a lot of companies into that dream, and I'm sorry to say, it hasn't really worked out for them,” he told BioWorld. Instead, Borriello said he envisioned a cell training platform that doesn’t just tweak a single immune pathway but instead harnesses multiple immune pathways to turn the tables on cancer.
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Australia reimburses Vazkepa a decade after US approval

Nov. 5, 2024
By Tamra Sami
For the first time, Australians have access to CSL Inc.’s Vazkepa (icosapent ethyl/Vascepa) for managing cardiovascular disease more than a decade after the drug was first approved in the U.S.
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FDA feedback shows Clarity path to pivotal radiopharma trial

Oct. 22, 2024
By Tamra Sami
Clarity Pharmaceuticals Ltd. will begin early next year its pivotal phase III trial for its copper-based radiopharmaceutical, 64Cu-SAR-bisPSMA, for diagnosing prostate cancer in patients with biochemical recurrence following positive U.S. FDA feedback.
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