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BioWorld - Saturday, May 30, 2026
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Home » Topics » BioWorld Asia, Australia

BioWorld Asia, Australia
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Green approved stamp

Pfizer vaccine receives provisional approval in Australia

Jan. 26, 2021
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) has granted provisional approval to Pfizer Australia Pty Ltd. for its COVID-19 vaccine, branded Comirnaty, making it the first COVID-19 vaccine to receive approval in Australia.
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Cyclopharm-Technegas-pic-1-26

Australia’s Cyclopharm raises AU$30M ahead of U.S. launch of Technegas for pulmonary embolism

Jan. 26, 2021
By Tamra Sami
PERTH, Australia – Sydney-based Cyclopharm Ltd. raised AU$30 million (US$23.19 million) in a private placement that will enable the company to launch its Technegas combination product in the U.S.
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Australia map, flag

Stakeholder survey: Drug and device companies laud TGA’s pandemic response but want process improvements

Jan. 19, 2021
By Tamra Sami
PERTH, Australia – The majority of medical device and biopharma industry respondents agreed that Australia’s Therapeutic Goods Administration (TGA) responded effectively to COVID-19, but they want to see the agency improve its processes to act faster and with more clarity, according to the TGA’s annual stakeholder survey.
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Australian flag on laptop screen with health professional

Australia advances infrastructure investments in diabetes, cardiovascular, regenerative therapies

Jan. 12, 2021
By Tamra Sami
PERTH, Australia – Australia’s Medical Technologies and Pharmaceuticals Industry Growth Center (MTPConnect) is boosting funding for the translation and commercialization of research in diabetes, cardiovascular disease and regenerative medicine.
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Australia and coronavirus

COVID-19 disrupted Australia’s business but the TGA still met its goals

Jan. 5, 2021
By Tamra Sami
PERTH, Australia – The COVID-19 pandemic certainly put pressure on Australia’s Therapeutic Goods Administration during the 2019 to 2020 year, but it also showed that the agency was able to rise to challenge and not buckle under pressure.
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Globe showing Australia

Australians pay less for drugs but must wait twice as long for access

Dec. 29, 2020
By Tamra Sami
PERTH, Australia – Although Australians pay less for their drugs than patients in many other countries, Australia is falling behind when it comes to reimbursement for newer, targeted therapies, according to a report launched by Medicines Australia that assessed the timelines for registration and reimbursement of new medicines in Australia compared to 10 other Organisation for Economic Co-operation and Development (OECD) countries.
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Chimeric closes AU$35M IPO to progress CAR T made from scorpion toxin

Dec. 15, 2020
By Tamra Sami
PERTH, Australia – Chimeric Therapeutics Ltd. closed an IPO on the Australian Securities Exchange (ASX:CHM), raising AU$35 million (US$26.5 million) to fund its CAR T trial in glioblastoma.
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Disintegrating coronavirus

CSL, University of Queensland quit COVID-19 vaccine trials due to HIV antibody response

Dec. 15, 2020
By Tamra Sami
PERTH, Australia – The University of Queensland (UQ) and CSL Ltd. are abandoning their trials of an Australian COVID-19 vaccine after recipients generated HIV antibodies during phase I trials. The response means the antibodies produced by the vaccine can interfere with HIV diagnostic tests. However, there was no possibility the vaccine caused infection, and routine follow-up tests confirmed no HIV virus was present, the partners said.
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Drugs-in-space-CubeLab-pic-11-19

University of Adelaide begins space odyssey into pharmaceutical stability

Nov. 24, 2020
By Tamra Sami
PERTH, Australia – As the idea of going to Mars starts to look less far-fetched, scientists are beginning to ask practical questions about how space affects the stability of drugs.
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Respiratory infection

Mesoblast licenses remestemcel-L to Novartis in deal worth up to $1.3B

Nov. 24, 2020
By Tamra Sami
PERTH, Australia – Mesoblast Ltd. inked an exclusive global licensing deal with Novartis AG for the development, manufacture and commercialization of Mesoblast’s mesenchymal stromal cell product remestemcel-L, with an initial focus on the acute respiratory distress syndrome, including that associated with COVID-19, just six weeks after the FDA issued a complete response letter for the therapy as a treatment for steroid-refractory acute graft-versus-host disease.
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