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BioWorld - Thursday, May 28, 2026
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Illustration of brain with electrical activity background

Brain Trust Bio’s drug delivery method to be tested in Australia

April 23, 2024
By Tamra Sami
Brain Trust Bio Inc. (BTB) will soon begin phase I trials in Australia of its IT-Riluzole delivered to the brain via a continuous intrathecal drug delivery method in people with amyotrophic lateral sclerosis. The company’s concept is to take known drugs that work and make them better by delivering them exclusively to where patients need them most, BTB co-founder and CEO Chen Benkler told BioWorld.
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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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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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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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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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Australian coins and bills

PYC’s AU$74M advancing RNA therapy for retinitis pigmentosa

March 19, 2024
By Tamra Sami
PYC Therapeutics raised AU$40 million of an anticipated AU$74 million (US$48.6 million) capital raise to advance three candidates, including lead candidate VP-001, which could potentially be the first treatment for retinitis pigmentosa type 11 (RP11), which causes blindness that begins in childhood and ultimately leads to legal blindness by middle age.
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Kidneys

Dimerix raises AU$20M on positive phase III kidney disease data

March 12, 2024
By Tamra Sami
Dimerix Ltd. announced a AU$20 million ($US13.22 million) capital raise following the news that its lead candidate, DMX-200, was successful in a prespecified interim analysis of the efficacy endpoint in its pivotal phase III trial in focal segmental glomerulosclerosis, a rare kidney disease.
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Illustration of motor neuron connecting to muscle fiber

Pivotal trial next for Pharmaust after MND/ALS phase I success

March 5, 2024
By Tamra Sami
Pharmaust Ltd.’s monepantel met its primary safety endpoints and showed positive signals of potential efficacy in a phase I trial in patients with motor neuron disease (MND)/amyotrophic lateral sclerosis (ALS). With these results, the company will now progress to a pivotal phase II/III trial by midyear, Pharmaust CEO Michael Thurn told BioWorld.
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