Kazia Therapeutics Limited, together with its subsidiaries, operates as an oncology-focused biotechnology company in Israel. The company's lead development candidate is paxalisib, a small molecule, brain-penetrant inhibitor of the phosphoinositide-3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) pathway, which is in Phase II/III clinical trial for the treatment of glioblastoma; in Phase II trial to treat isocitrate dehydrogenase-mutant glioma, primary central nervous system (CNS) lymphoma, diffuse intrinsic pontine glioma, and brain metastases; and in pre-clinical studies to treat triple-negative breast cancer, as well as for the treatment of atypical rhabdoid/teratoid tumors. It also develops EVT801, a small-molecule selective inhibitor of vascular endothelial growth factor receptor 3 that is in Phase I clinical trial to treat advanced solid tumors and ovarian cancer. The company has collaborations with the Australian and New Zealand Children’s Haematology/Oncology Group, Genentech Inc., Global Coalition for Adaptive Research, Vivesto AB, Simcere Pharmaceutical Group Ltd, Evotec SE, Sovargen Co., Ltd, and QIMR Berghofer Medical Research Institute. Kazia Therapeutics Limited was formerly known as Novogen Limited and changed its name to Kazia Therapeutics Limited in November 2017. Kazia Therapeutics Limited was incorporated in 1994 and is based in Sydney, Australia.
Kazia Therapeutics Announces Sovargen Co. Doses First Patient in Phase 1b/2a Trial of Paxalisib for Rare Seizure Disorders
Sovargen has dosed the first patient in a Phase 1b/2a trial of paxalisib for intractable epilepsy linked to focal cortical dysplasia type 2 and tuberous sclerosis complex, triggering a $2 million development milestone payment to Kazia.
Under the March 2024 exclusive licensing deal, Sovargen develops and commercializes paxalisib for mTORopathy-related epilepsies worldwide excluding mainland China, Hong Kong, Macao and Taiwan; Kazia remains eligible for up to $17 million in further milestones plus sub-licensing revenue share and royalties on net sales.
For Kazia, the milestone adds non-dilutive cash and external validation of paxalisib's mechanism beyond oncology, while the company's own clinical focus for the asset stays on cancer, including post-GBM AGILE registrational planning.