Kazia Therapeutics (KZIA): Phase IIa Shows Good Safety, Consistent Efficacy
Kazia's latest interim data analysis from its Phase IIa study of paxalisib in glioblastoma multiforme (GBM) shows promising results. The study reports progression-free survival (PFS) of 8.4 months and overall survival (OS) of 17.5 months. The safety data at the full 60mg dose indicates a favorable profile. Additionally, Kazia increased its valuation to US$184 million or US$14.55 per ADR, reflecting higher success probability for paxalisib. This adjustment follows an October US$18 million capital raise, enhancing investor outlook.
- PFS of 8.4 months and OS of 17.5 months reported for paxalisib.
- Safety profile of paxalisib at 60mg dose shows favorable results.
- Valuation increased to US$184 million from US$104 million.
- Probability of success for paxalisib raised to 35% from 20%.
- Completed an US$18 million capital raise, strengthening financial position.
- None.
LONDON, UK / ACCESSWIRE / December 3, 2020 / Kazia presented the results from a new interim data analysis of its ongoing Phase IIa study of paxalisib in glioblastoma multiforme (GBM). The data were consistent with previous data and showed progression-free survival (PFS) of 8.4 months and overall survival (OS) of 17.5 months. Importantly, Kazia also published some of the first safety data at the full 60mg dose, which show an attractive profile compared to other members of this class.
We have increased our valuation to US
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https://www.accesswire.com/619154/Kazia-Therapeutics-KZIA-Phase-IIa-Shows-Good-Safety-Consistent-Efficacy
FAQ
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