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BioWorld - Sunday, March 8, 2026
Home » Topics » Asia-Pacific » Australia

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Australia and coronavirus

Australia’s device and biotech companies hold the key for future pandemic preparedness: MTPConnect report

Oct. 15, 2020
By Tamra Sami
PERTH, Australia – During the COVID-19 pandemic, 90% of Australia’s clinical trials were put on hold, and the market cap of biotech and medical device companies on the Australian Securities Exchange dropped 5% to AU$11 billion (US$7.78 billion), according to a recent report by Australia’s Medical Technologies and Pharmaceuticals Industry Growth Centre.
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Product image

Astrazeneca strikes deal with Impedimed for Sozo platform in heart failure, kidney disease trial

Oct. 13, 2020
By Tamra Sami
PERTH, Australia – Astrazeneca plc is leasing 175 Sozo devices from Impedimed Ltd. and plans to put them in 20 countries to run phase II trials for a combination drug that looks at fluid imbalance in the human body in patients with heart failure (HF) and chronic kidney disease.
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Diagram of device components

Australia’s Epi-Minder raises AU$18M series A to test seizure monitoring device

Oct. 9, 2020
By Tamra Sami
PERTH, Australia – Epi-Minder Pty. Ltd. has completed an oversubscribed series A round of AU$18 million (US$12.89 million) that will see its Minder epilepsy monitoring device enter a pivotal trial to support marketing applications in Europe and the U.S. The smartphone-enabled device promises to improve on wearables and other tools – such as patient diaries – that have proven to be unreliable.
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CEO holding Febridx

Lumos Diagnostics nabs $17.9M for rapid POC test

Oct. 7, 2020
By Meg Bryant
Lumos Diagnostics Holdings Pty. Ltd. scooped up AU$25 million (US$17.9 million) in an oversubscribed pre-IPO ahead of its anticipated 2021 listing on the Australian Securities Exchange (ASX). The funds will be used to expand manufacturing operations in California and Florida and to grow the commercial footprint of Febridx, a rapid point-of-care (POC) test that can determine if a person has a viral or bacterial infection within 10 minutes.
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Product image

Astrazeneca strikes deal with Impedimed for Sozo platform in heart failure, kidney disease trial

Oct. 7, 2020
By Tamra Sami
PERTH, Australia – Astrazeneca plc is leasing 175 Sozo devices from Impedimed Ltd. and plans to put them in 20 countries to run phase II trials for a combination drug that looks at fluid imbalance in the human body in patients with heart failure (HF) and chronic kidney disease.
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Jackie Fairley, CEO, Starpharma

Starpharma completes AU$45M placement to accelerate development of COVID-19 nasal spray

Oct. 6, 2020
By Tamra Sami
PERTH, Australia – Starpharma Holdings Ltd. completed a AU$45 million (US$32 million) placement to domestic and international investors that will see it advance its COVID-19 antiviral nasal spray. The treatment is based on the company’s antiviral dendrimer, SPL-7013.
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Stem cells

Mesoblast stock tanks on news of FDA CRL for Ryoncil BLA in pediatric GVHD

Oct. 6, 2020
By Tamra Sami
PERTH, Australia – Regenerative medicine company Mesoblast Ltd. saw its stock drop 37% on the news that it received an FDA complete response letter to its BLA for Ryoncil (remestemcel-L) for the treatment of pediatric steroid-refractory acute graft-vs.-host disease.
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Product image

Astrazeneca strikes deal with Impedimed for Sozo platform in heart failure, kidney disease trial

Oct. 6, 2020
By Tamra Sami
PERTH, Australia – Astrazeneca plc is leasing 175 Sozo devices from Impedimed Ltd. and plans to put them in 20 countries to run phase II trials for a combination drug that looks at fluid imbalance in the human body in patients with heart failure (HF) and chronic kidney disease.
Read More
Stem cells

Mesoblast stock tanks on news of FDA CRL for Ryoncil BLA in pediatric GVHD

Oct. 2, 2020
By Tamra Sami
PERTH, Australia – Regenerative medicine company Mesoblast Ltd. saw its stock drop 37% on the news that it received an FDA complete response letter to its BLA for Ryoncil (remestemcel-L) for the treatment of pediatric steroid-refractory acute graft-vs.-host disease.
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Australia map, flag

Australia opens consultations on beefing up device adverse event reporting, UDI system

Oct. 1, 2020
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) is seeking industry feedback on further strengthening reforms for adverse events and postmarket regulations for medical devices.
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