Dizal to Highlight its Portfolio Advances in Hematologic Malignancies and Lung Cancer at ASCO 2025
- On May 26, 2025, Dizal shared clinical trial findings for its investigational agents DZD8586 and DZD6008 during the ASCO Annual Meeting held in Shanghai.
- These presentations stem from phase I/II studies addressing resistance in hematologic malignancies and EGFR-mutated NSCLC patients with limited existing treatments.
- DZD8586 achieved a response in 84.2% of heavily treated CLL/SLL patients, including those harboring BTK resistance mutations, while DZD6008 exhibited sustained antitumor effects alongside a favorable safety profile in patients with EGFR-mutated NSCLC.
- DZD8586 targets both BTK-dependent and-independent pathways with a 9-month duration of response rate of 83.3%, and DZD6008 achieved target lesion shrinkage in 83.3% of enrolled patients, per oral abstracts presented.
- These data reinforce Dizal's R&D strengths and support advancing both therapies to address unmet needs in blood cancers and lung cancer resistant to current treatments.
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Dizal to Highlight its Portfolio Advances in Hematologic Malignancies and Lung Cancer at ASCO 2025
DZD8586 demonstrated significant anti-tumor efficacy in heavily pretreated chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) patients with ORR of 84.2%DZD6008, a BBB-penetrant 4th generation EGFR TKI, showed encouraging and durable anti-tumor activity with favorable safety and tolerability as a monotherapy in…
Dizal to Highlight its Portfolio Advances in Hematologic Malignancies and Lung Cancer at ASCO 2025 - PressReach
DZD8586 demonstrated significant anti-tumor efficacy in heavily pretreated chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) patients with ORR of 84.2% DZD6008, a BBB-penetrant 4th generation EGFR TKI, showed encouraging and durable anti-tumor activity with favorable safety and tolerability as a monotherapy in heavily pre-treated non-small cell lung cancer (NSCLC) patients with EGFR-mutations SHANGHAI, May 26, 2025 /PRNewswire/ —…
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