Timetable
The proposed timetable for the satisfaction of conditions and the expected date of removal of the Company from the Official List are as follows:
| | |
Event | | Indicative Date* |
Notification of intention to delist | | 11 October 2023 |
Despatch of letters and ADS Conversion Facility election forms to shareholders | | 12 October 2023 |
Closing Date: Participation in ADS Conversion Facility | | 10 November 2023 |
Last day for trading of the Company’s Shares on ASX | | 10 November 2023 |
Completion of removal of the Company from the Official List of the ASX | | 14 November 2023 |
* | Dates and times are indicative only and subject to change by the Company or ASX. |
Shares may continue to be traded on ASX up until the last trading day, after which trading will be suspended until the Delisting on the next trading day.
This announcement was authorised for release by the Board.
Inquiries:
Company Matters Pty Limited
cosec@companymatters.com.au
About Kazia Therapeutics Limited
Kazia Therapeutics Limited (NASDAQ: KZIA; ASX: KZA) is an oncology-focused drug development company, based in Sydney, Australia.
Our lead program is paxalisib, a brain-penetrant inhibitor of the PI3K / Akt / mTOR pathway, which isbeing developed to treat multiple forms of brain cancer. Licensed from Genentech in late 2016, paxalisib is or has been the subject of ten clinical trials in this disease. A completed Phase II study in glioblastoma reported promising signals of clinical activity in 2021, and a pivotal study in glioblastoma, GBM AGILE, is ongoing, with final data expected in CY2023. Other clinical trials are ongoing in brain metastases, diffuse midline gliomas, and primary CNS lymphoma, with several of these havingreported encouraging interim data.
Paxalisib was granted Orphan Drug Designation for glioblastoma by the US FDA in February 2018, andFast Track Designation (FTD) for glioblastoma by the FDA in August 2020. Paxalisib was also awarded (FTD) in July 2023 for the treatment of solid tumour brain metastases harbouring PI3K pathway mutations in combination with radiation therapy. In addition, paxalisib was granted Rare Pediatric Disease Designation and Orphan Drug Designation by the FDA for diffuse intrinsic pontine glioma in August2020, and for atypical teratoid / rhabdoid tumours (AT/RT) in June 2022 and July 2022, respectively.
Kazia is also developing EVT801, a small-molecule inhibitor of VEGFR3, which was licensed from Evotec SE in April 2021. Preclinical data has shown EVT801 to be active against a broad range of tumour types and has provided compelling evidence of synergy with immuno-oncology agents. A Phase I study commenced recruitment in November 2021.
For more information, please visit www.kaziatherapeutics.com or follow us on Twitter @KaziaTx.