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Kazia Presents Further Paxalisib and Cantrixil Data at AACR, Reinforcing Positive Efficacy Signals for both Drugs

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Kazia Therapeutics Limited (ASX: KZA; NASDAQ: KZIA) presented interim data at the AACR Annual Meeting, showcasing promising results for paxalisib in glioblastoma and Cantrixil in ovarian cancer. The phase II study of paxalisib, now with data on 30 patients, showed a progression-free survival (PFS) of 8.5 months and overall survival (OS) of 17.7 months. In the Cantrixil study, one complete response and two partial responses were noted, leading to an overall response rate of 19%. The company plans to commence pivotal studies for paxalisib in late 2020.

Positive
  • Paxalisib shows a PFS of 8.5 months and OS of 17.7 months, indicating improved efficacy over the standard treatment, Temozolomide (5.3 months PFS, 12.7 months OS).
  • Cantrixil demonstrated one complete response and two partial responses, achieving a 19% overall response rate among evaluable patients.
  • Interim data from the phase I study of paxalisib with radiotherapy indicated a 'robust response' in the initial treated patient.
Negative
  • None.

SYDNEY, June  22, 2020 /PRNewswire/ -- Kazia Therapeutics Limited (ASX: KZA; NASDAQ: KZIA), an Australian oncology-focused biotechnology company, is pleased to share poster presentations of interim data from the ongoing phase II study of paxalisib (formerly GDC-0084) in glioblastoma, the most common and most aggressive form of primary brain cancer, and from the phase I study of Cantrixil in ovarian cancer.

"Kazia

Key Points

  • Previous paxalisib data presented at ASCO was based on Stage 1 (n=9) of the ongoing phase II study in glioblastoma. This interim analysis at AACR includes all patients in the study (n=30), and therefore provides a more robust and substantial data set
  • Progression-free survival (PFS) for paxalisib is 8.5 months, versus 8.4 months in the previous analysis
  • Paxalisib overall survival (OS) remains at 17.7 months, in line with ASCO data
  • A separate poster on the investigator-initiated study of paxalisib in combination with radiotherapy is presented by clinicians at Memorial Sloan Kettering Cancer Center in New York. It noted a 'robust response' in the first treated patient
  • Cantrixil data shows one complete response (CR) to treatment, meaning no measurable disease, and two partial responses (PR), for an overall response rate of 19% (3 / 16 evaluable patients)

Summary of Paxalisib Data in Comparison to Temozolomide (existing standard of care)


Temozolomide[1]
(FDA-approved treatment)

Paxalisib

(interim phase II data)

Progression-Free Survival (PFS)

5.3 months

8.5 months

Overall Survival (OS)

12.7 months

17.7 months

Kazia CEO, Dr James Garner, commented, "The data summarized in these posters help to strengthen our confidence in both our clinical programs. As paxalisib moves towards commencement of the GBM AGILE pivotal study in the second half of calendar 2020, these findings will be used to support set-up activities. In the meantime, the fact that the PFS has remained robust as the analysis is extended out to the full data set gives us a great deal of additional confidence in the efficacy signal it provides. For Cantrixil, the emergence of one complete responder (CR) to treatment is very positive, and these new results will help us to explore partnering opportunities over the second half of the year."

AACR Annual Meeting

The American Association of Cancer Research (AACR) Annual Meeting is one of the leading global academic conferences for oncology research. It is typically attended by more than 20,000 clinicians, researchers, industry executives, and investors, representing over 140 countries. The conference is being conducted through a virtual format this year and has been broken into two sections. AACR Virtual Meeting I took place 27-28 April 2020, and AACR Virtual Meeting II is being held 22-24 June 2020.

The paxalisib poster is found under number CT205 (NCT03522298), and the Cantrixil poster under CT166 (NCT02903771). Registration to the virtual meeting is free and interested parties may register via the AACR website. The posters can be viewed on our website:

https://kza.irmau.com/irm/PDF/42fa1764-4329-42d8-9fbc-c9e2433b3ecc/PaxalisibposterpresentedatAACRvirtualmeeting

https://kza.irmau.com/irm/PDF/e55c6c96-c2c8-4aa1-ad7f-369d771857ca/CantrixilposterpresentedatAACRvirtualmeeting

Initial Data from Memorial Sloan-Kettering Study of Paxalisib with Radiotherapy

Dr Jonathan Yang and team at Memorial Sloan Kettering Cancer Center in New York, NY, also presented a poster (number CT252) on their ongoing phase I study of paxalisib in combination with radiotherapy (NCT04192981). The poster principally reported the design of their study, but also noted a 'robust response' in the first patient treated. Further data is expected as the study progresses

Next Steps

The paxalisb phase II study remains ongoing with a number of patients in follow-up and approximately half of the total enrolled patient population still receiving drug at the time of analysis. Kazia expects to complete the study in 1H CY2021.

Set-up work is well underway for paxalisib's planned entry into the GBM AGILE pivotal study, and it is expected that the first patient will be enrolled in the second half of calendar 2020.

The Cantrixil phase I study is now complete and analysis is underway, with final data expected in the second half of calendar 2020.

[1] ME Hegi, A-C Desirens, T Gorlia, et al. N Engl J Med (2005); 352:997-1003

 

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SOURCE Kazia Therapeutics Ltd

FAQ

What were the key findings from the AACR presentation by Kazia Therapeutics on paxalisib?

The AACR presentation revealed that paxalisib achieved a progression-free survival of 8.5 months and an overall survival of 17.7 months in glioblastoma patients.

How does paxalisib compare to Temozolomide?

Paxalisib showed improved progression-free survival (8.5 months) and overall survival (17.7 months) compared to Temozolomide, which had a PFS of 5.3 months and OS of 12.7 months.

What were the results for Cantrixil in ovarian cancer?

Cantrixil displayed one complete response and two partial responses, resulting in a 19% overall response rate among 16 evaluable patients.

What are the next steps for Kazia Therapeutics regarding paxalisib?

Kazia plans to begin the GBM AGILE pivotal study for paxalisib in the second half of 2020.

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