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BioWorld - Saturday, April 18, 2026
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Home » Topics » BioWorld Asia, Australia

BioWorld Asia, Australia
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As bushfires continue to burn, Australia’s regulators don’t anticipate delays

Jan. 14, 2020
By Tamra Sami
PERTH, Australia – Although Australia’s deadly bushfires continue to burn, Australia’s Therapeutic Goods Administration (TGA) is not anticipating any effect on business operations.
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Hospital bed, room

Australia implements opioid reforms to deal with 150 hospitalizations per day

Jan. 7, 2020
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration is putting in place a number of opioid reforms to clamp down on the use of opioids to deal with increasing deaths and hospitalizations from the use of those drugs.  
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Globe showing Australia

Australia unveils new companion diagnostics regulatory framework

Dec. 24, 2019
By Tamra Sami
Following lengthy consultations with industry, Australia’s Therapeutic Goods Administration (TGA) has released its new regulatory framework for in vitro companion diagnostics (IVD CDx) that becomes effective in February. Until now, Australia did not have a framework for CDx.
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Liver disease

Boehringer Ingelheim quits development of Pharmaxis drug for NASH indication

Dec. 24, 2019
By Tamra Sami
PERTH, Australia – Boehringer Ingelheim GmbH is discontinuing development of BI-1467335 for the treatment of nonalcoholic steatohepatitis (NASH) that it acquired from Sydney-based Pharmaxis Ltd. in 2015.
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Chinese investors launch new AU$45M fund to develop South Australian biotech

Dec. 17, 2019
By Tamra Sami
PERTH, Australia – Private Chinese investors have launched a new AU$45 million (US$31.17 million) investment fund to accelerate the development and commercialization of new biotechnology from South Australia for the global market.
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Australia’s R&D tax incentive threatened yet again

Dec. 10, 2019
By Tamra Sami
PERTH, Australia – Despite a Senate inquiry recommendation to hold off on introducing cuts to Australia’s Research and Development Tax Incentive (RDTI), a bill that recommends cuts was introduced in Parliament, sending shudders through the biotech industry. “Ausbiotech is deeply concerned that the RDTI Bill has been reintroduced, despite the Senate Committee’s recommendations to defer consideration of the bill until further examination and analysis of the impact is undertaken,” said Ausbiotech CEO Lorraine Chiroiu.
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Digital eye illustration

Australia’s Opthea raises AU$50M to advance OPT-302 to phase III in wet AMD

Dec. 3, 2019
By Tamra Sami
PERTH, Australia – On the heels of positive phase IIb data, Opthea Ltd. announced a private placement of AU$50 million (US$33.87 million) from institutional investors in Australia and the U.K. to advance lead candidate OPT-302 to phase III trials in wet AMD.
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3D head brain cancer

Australia’s Kazia Therapeutics reports positive interim results in phase II glioblastoma trial

Nov. 26, 2019
By Tamra Sami
PERTH, Australia – Sydney-based Kazia Therapeutics Ltd.’s shares soared nearly 82% this week on positive interim results for lead molecule GDC-0084 in a phase II glioblastoma trial. Data from the first nine patients in the study show that GDC-0084 treatment resulted in a median progression-free survival (PFS) rate of 8.4 months compared to the standard of care, temozolomide, which has a PFS of around 5.3 months.
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Australian flag marking country on globe
AusBiotech 201

National stem cell roadmap provides cohesive vision, funding for Australia's regenerative medicine sector

Nov. 12, 2019
By Tamra Sami
MELBOURNE, Australia – Although Australia was one of the first movers in the regenerative medicine space, until now a cohesive plan for investing in regenerative medicine was holding the sector back.
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Globe showing Australia
AusBiotech 2019

Australia's biotechs grapple with reimbursement system for cell therapies

Nov. 6, 2019
By Tamra Sami
Although Australia's Therapeutic Goods Administration (TGA) approved its first CAR T therapy in 2018, the country is lacking a system to reimburse those advanced therapies, and industry is calling on government to revalue gene therapies.
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