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BioWorld - Saturday, April 25, 2026
Home » Topics » Asia-Pacific » Australia

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Child drawing with pencil

Neurotech’s NTI-164 meets endpoints in pediatric autism trial

April 17, 2024
By Tamra Sami
Neurotech International Ltd.’s cannabinoid NTI-164 met the primary and secondary endpoints in a phase II/III trial in children with autism spectrum disorder. The company also reported positive top-line data for Rett syndrome in a phase I/II trial.
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Conceptual image for brain cancer treatment

Radiopharma glioma imaging agent fast-tracked as Telix preps NDA

April 16, 2024
By Tamra Sami
The U.S. FDA granted fast track designation to Telix Pharmaceutical Ltd.’s TLX101-CDx for glioma imaging as the firm prepares to file its NDA in the first half of 2024, a Telix spokesperson told BioWorld.
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SpeeDx Diagnostics

Speedx launches qPCR panel to detect 14 different viruses

April 10, 2024
By Tamra Sami
Australia’s Speedx Pty Ltd. is launching a new rapid polymerase chain reaction (qPCR) test for 14 different respiratory viruses in a single test that works on almost every commercial PCR platform in half the time and at a fraction of the cost of what its competitors charge.
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Golden dollar coins

Medicxi, Starpharma create Petalion with $25M round

April 9, 2024
By Tamra Sami
A day after investing $40 million in China’s D3 Bio Inc., London-based venture capital firm Medicxi is investing $25 million to co-found a new U.K.-based company called Petalion Therapeutics Ltd. that will focus on an early stage oncology asset from Australia’s Starpharma Holdings Ltd. to develop novel dendrimer-based treatments.
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Australia’s anti-trust watchdog clears Cohlear-Oticon revised deal

April 4, 2024
By Tamra Sami
Australia’s Competition and Consumer Commission said it will not oppose Cochlear Ltd.’s proposed acquisition of the cochlear implants business of Denmark’s Oticon A/S after the bone conduction businesses was removed from the deal.
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DNA mutations or genetic disorder concept art
Dermatologic

Australian researchers discover gene mutation that causes psoriasis

April 2, 2024
By Tamra Sami
Scientists from the Australian National University have discovered the gene mutation responsible for causing psoriasis, and the findings could lead to improved diagnosis and treatment for patients with psoriasis and psoriatic arthritis, a chronic inflammatory skin disease. “We were able to identify the gene that could be important in enabling this progression from a skin-only condition to a skin-and-joint condition,” lead study author Chelisa Cardinez told BioWorld.
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DNA mutations or genetic disorder concept art
Dermatologic

Australian researchers discover gene mutation that causes psoriasis

March 27, 2024
By Tamra Sami
Scientists from the Australian National University have discovered the gene mutation responsible for causing psoriasis, and the findings could lead to improved diagnosis and treatment for patients with psoriasis and psoriatic arthritis, a chronic inflammatory skin disease. “We were able to identify the gene that could be important in enabling this progression from a skin-only condition to a skin-and-joint condition,” lead study author Chelisa Cardinez told BioWorld.
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Clarity technology platform

Clarity adds AU$121M for radiopharma pipeline of copper therapies

March 26, 2024
By Tamra Sami
Clarity Pharmaceuticals Ltd. raised AU$121 million (US$79.29 million) through a private placement that will fund the company’s radiopharma pipeline comprising targeted copper therapies out to early 2026.
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Kazia licenses rare epilepsy drug paxalisib to Korea’s Sovargen

March 26, 2024
By Tamra Sami
Kazia Therapeutics Ltd. has out-licensed paxalisib as a potential treatment for intractable epilepsy in focal cortical dysplasia type 2 and tuberous sclerosis complex disease in a carve-out deal with Sovargen Co. Ltd. for $20.5 million plus sales royalties.
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Mesoblast rockets on FDA’s acceptance of trial data for GVHD BLA

March 26, 2024
By Tamra Sami
Regenerative medicine company Mesoblast Ltd. saw its stock shoot up 45% on the news that the U.S. FDA is satisfied with the additional data submitted from the company’s phase III study for remestemcel-L for treatment of adults with steroid-refractory acute graft-vs.-host disease (SR-aGVHD) to support filing a BLA in pediatric patients with SR-aGVHD.
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