Combination therapy with a raf inhibitor and a cdk4/6 inhibitor for use in the treatment of cancer
A technology for inhibitors and cancer, applied in the field of drug combinations, can solve problems such as off-target toxicity and unmet medical needs
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example 1
[0177] Example 1: Combination of RAF Inhibition and Enhancement of CDK4 / CDK6 Inhibition in NRAS Mutant Melanoma Cell Lines
[0178] method
[0179] A compound of formula (I) (NVP-LXH254) and ribociclib (NVP-ribociclib) were synthesized, and a compound stock solution of ribociclib was prepared in DMSO at a final concentration of 10 mM. For combination assays, the working stock was serially diluted in appropriate cell culture media in 3-fold increments (2-fold increments for ribociclib) to achieve final assay concentrations: NVP-LXH254 ranged from 10 μM to 1.5 nM, 10 μM to 39 nM (succinate form) for NVP-ribociclib.
[0180] SK-MEL-2 cells were purchased from American Type Culture Collection (ATCC), MEL-JUSO cells were purchased from German Microbiology and Cell Culture Series Co., Ltd. (DSMZ), MM415 cells were purchased from Australian Cell Bank, and IPC-298 and SK- MEL-30 cells were obtained from GNF. IPC-298, MEL-JUSO, MM415, and SK-MEL-30 cells were cultured in RPMI medium...
example 2
[0187] Example 2: Combination Efficacy of Compounds of Formula (I) and Ribociclib in Xenografts Derived from NRAS Mutant Melanoma Patients
[0188] The effect of selective dual RAF and CDK4 / 6 inhibition in vivo was investigated by combining a compound of formula (I) and ribociclib in nine xenografts derived from NRAS mutant melanoma patients.
[0189] method
[0190] Animal and Maintenance Conditions: At least 3 days prior to manipulation, outbred athymic (nu / nu) female mice (Athymic Nude-nu") (Charles River, Indianapolis, Indianapolis) were allowed ad libitum access to food and water. The Novartis NIBR animal facility was adapted to the new environment (Table 1).
[0191] Table 1 Animal characteristics
[0192]
[0193] Statement on animal welfare: Animals were handled in accordance with Novartis NIBR ACUC regulations and guidelines.
[0194] Test compounds and formulations: Compounds of formula (I) (free base form) in MEPC4 vehicle (45% Cremophor RH40+27% PEG400+18% co...
example 3
[0225] Example 3: Phase Ib, open-label, multicentre study of a compound of formula (I) in combination with ribociclib in patients with NRAS-mutant melanoma
[0226] The purpose of this study was to characterize the safety and tolerability of the dual combination of a compound of formula (I) and ribociclib in patients with NRAS-mutant melanoma and to determine the recommended dose.
[0227] The primary endpoint is
[0228] (1) Safety: Incidence and severity of adverse events (AEs) and serious AEs (SAEs), including changes in laboratory values, vital signs, and electrocardiogram (ECG), dose restrictions during cycle 1 (dose escalation only) The incidence and nature of toxicity (DLT),
[0229] (2) Tolerance: dose interruption, reduction and dose intensity.
[0230] Secondary objectives and endpoints are:
[0231] (a) Evaluation of the initial antitumor activity of a compound of formula (I) in combination with ribociclib. Overall response rate (ORR), disease control rate (DCR)...
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