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Last updated: 2021-03-14

(Solid Tumors) M6620 (VX-970) Monotherapy and Combination Therapy Effective?

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(Solid Tumors) M6620 (VX-970) Monotherapy and Combination Therapy Effective?

(Solid Tumors) M6620 (VX-970) Monotherapy and Combination Therapy Effective?

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On June 22, 2020, Timothy A. Yap published in the medical journal Journal of Clinical Oncology the efficacy and safety results of ATR inhibitor M6620 (VX-970) monotherapy and M6620 + carboplatin combination therapy in previously treated patients with advanced solid tumors in a Phase 1 clinical trial.

This Phase 1 trial randomly assigned previously treated patients with advanced solid tumors into two groups. Primary endpoint: safety and tolerability; secondary endpoint: anti-tumor activity.

  • M6620 (VX-970) monotherapy group (1–2 times per week, M6620 60–240 mg/m²; N=17)
  • M6620 (VX-970) combination therapy group (once per week, M6620 90–240 mg/m² + carboplatin; N=23)

Safety results: Grade 3 or higher adverse events — M6620 monotherapy group 5.9% (N=1); M6620 combination group 30.4% (N=7). Overall adverse event rate — M6620 monotherapy group 88.2% (N=15); M6620 combination group 91.3% (N=21).

Based on these safety results, the recommended Phase 2 doses were determined: M6620 monotherapy group (1–2 times per week, M6620 240 mg/m²); M6620 combination group (once per week, M6620 90 mg/m² + carboplatin).

Anti-tumor efficacy results (secondary endpoint): In the M6620 monotherapy group (N=17 evaluable): 1 complete response, 5 stable disease. In the M6620 combination group (N=21 evaluable): 1 partial response, 15 stable disease.

Based on Phase 1 trial results, Timothy A. Yap concluded: In previously treated patients with advanced solid tumors, ATR inhibitor M6620 (VX-970) monotherapy and M6620 + carboplatin combination therapy showed good tolerability and confirmed anti-tumor activity.

Source: Phase I Trial of First-in-Class ATR Inhibitor M6620 (VX-970) as Monotherapy or in Combination With Carboplatin in Patients With Advanced Solid Tumors (J Clin Oncol. 2020 Jun 22; JCO1902404. doi: 10.1200/JCO.19.02404.)

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