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BioWorld - Monday, May 4, 2026
Home » Topics » Asia-Pacific » Australia

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Map of Australia with pills, vials and syringe

Australia delivers new National Medicines Policy aiming to deliver greater access to medicines

Dec. 28, 2022
By Tamra Sami
The Australian government delivered an early Christmas present to the biopharma industry in the form of a new National Medicines Policy giving voice to major industry goals – among them a clear vision to “achieve the world’s best health, social and economic outcomes for all Australians through a highly supportive medicines policy environment.”
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Stentrode device

Australia’s Synchron raises AU$110M to advance endovascular brain computer interface

Dec. 20, 2022
By Tamra Sami
Medical technology company Synchron Inc. completed an AU$110 million (US$73.9 million) series C round that will allow the company to conduct a feasibility study and pivotal trial of its implantable brain computer interface that can interpret and stimulate parts of the brain.
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Ovarian cancer illustration

Inoviq study confirms utility of exosome-based ovarian cancer screening diagnostic

Dec. 15, 2022
By Tamra Sami
A feasibility study conducted by the University of Queensland (UQ) confirmed the utility of Inoviq Ltd.’s exosome-based ovarian cancer screening test for isolating extracellular vesicle (EV) biomarkers. The Ovarian Cancer 97 study (OC97) screened data from 97 plasma samples and identified significant differences between the EV biomarker content of ovarian cancer and healthy control samples.
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Vaxxas HD-MAP vaccine application

Vaxxas raises $23M to advance needle-free COVID-19 vaccines

Dec. 13, 2022
By Tamra Sami
Vaxxas Pty. Ltd. raised AU$34 million (US$23 million) to advance its needle-free COVID-19 vaccine program, which began in early November, and readouts from the study are expected in late February or early March, Vaxxas CEO David Hoey told BioWorld. The COVID-19 vaccine patch is based on the company’s high-density microarray patch technology that delivers Hexapro, a second-generation version of the spike protein used in all major U.S.-approved COVID-19 vaccines.
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Vaxxas HD-MAP vaccine application

Vaxxas raises $23M to advance needle-free COVID-19 vaccines

Dec. 9, 2022
By Tamra Sami
Vaxxas Pty. Ltd. raised AU$34 million (US$23 million) to advance its needle-free COVID-19 vaccine program, which began in early November, and readouts from the study are expected in late February or early March, Vaxxas CEO David Hoey told BioWorld. The COVID-19 vaccine patch is based on the company’s high-density microarray patch technology that delivers Hexapro, a second-generation version of the spike protein used in all major U.S.-approved COVID-19 vaccines.
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Antibiotic resistant bacteria inside a biofilm
Infection

Researchers identify new class of antibiotic resistance mechanism

Dec. 8, 2022
By Mar de Miguel
When a drug prevents bacteria from synthesizing their own folate, an essential compound for their survival, they take it directly from the host. This antibiotic resistance mechanism had not been detected until now because bacteria behave differently in the laboratory than they do in vivo during an infection.
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Radiotherapy of cancer

How equipped are radiopharma stakeholders to overcome radioactive challenges?

Nov. 22, 2022
By Tamra Sami
Global interest in radiopharmaceuticals is growing, and some big deals in the space have sparked interest in the last few years. Novartis AG has spent about $6 billion in acquisitions and is seen as the global leader.
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Radiotherapy of cancer

How equipped are radiopharma stakeholders to overcome radioactive challenges?

Nov. 21, 2022
By Tamra Sami
Global interest in radiopharmaceuticals is growing, and some big deals in the space have sparked interest in the last few years. Novartis AG has spent about $6 billion in acquisitions and is seen as the global leader.
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Xray showing lung cancer on tablet

Immutep’s LAG-3 efti, with pembrolizumab, meets primary endpoint in first-line NSCLC

Nov. 15, 2022
By Tamra Sami
Immutep Ltd.’s lead immunotherapy candidate eftilagimod (IMP-321, efti) met the primary endpoint in its phase II trial evaluating the combination of efti and Merck & Co. Inc.’s Keytruda (pembrolizumab) as first-line treatment of non-small-cell lung cancer (NSCLC), reporting final data that show an overall response rate of 40.4%.
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Health professional recording info from patient

Que sees phase II success in reducing hot flashes after breast cancer

Nov. 15, 2022
By Tamra Sami
Que Oncology Inc.’s Q-122 significantly reduced the frequency and severity of moderate and severe vasomotor symptoms, or hot flashes, in women taking endocrine therapy for breast cancer, and phase II results showed associated improvement in quality of life, compared with placebo.
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