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BioWorld - Tuesday, January 27, 2026
Home » Authors » Tamra Sami

Tamra Sami

Articles

ARTICLES

Boehringer Ingelheim quits development of Pharmaxis drug for NASH indication

Dec. 18, 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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Chinese investors launch new AU$45M fund to develop South Australian biotech

Dec. 16, 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. The Adelaide China Biotech Investment Fund is backed by a group of private investors based in Nanjing, China, underwritten by the Bank of Nanjing.
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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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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. 
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TGA goes back to the drawing board again with guidance on custom-made and 3D-printed devices

Dec. 6, 2019
By Tamra Sami
PERTH, Australia – Industry was supportive of most of the changes proposed by Australia’s Therapeutic Goods Administration (TGA) for custom-made and 3D-printed devices. However, the comments also indicated that the current regulatory requirements for custom-made devices are not well understood. The agency stressed that increasing use of 3D printing for medical applications is raising questions about the adequacy of the current medical device regulatory framework to mitigate risks to patients.
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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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Ear illustration

FDA gives thumbs up to Cochlear’s implantable bone conduction hearing system

Dec. 3, 2019
By Tamra Sami
The U.S. FDA has cleared Cochlear Ltd.’s newest cochlear implant, the Osia 2 system, an active implantable bone conduction hearing system. Unlike Cochlear’s traditional implant, the Osia implant bypasses damaged parts of the ear and sends sound vibrations directly to the cochlea.
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Australia’s Opthea raises AU$50M to advance OPT-302 to phase III in wet AMD

Dec. 2, 2019
By Tamra Sami
PERTH, Australia – On the heels of positive phase IIb data, Melbourne-based 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 age-related macular degeneration (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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View All Articles by Tamra Sami

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