WO2025202971 - KRAS G12C INHIBITOR FOR USE FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER

National phase entry is expected:
Publication Number WO/2025/202971
Publication Date 02.10.2025
International Application No. PCT/IB2025/053263
International Filing Date 27.03.2025
Title **
[English] KRAS G12C INHIBITOR FOR USE FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER
[French] INHIBITEUR DE KRAS G12C DESTINÉ À ÊTRE UTILISÉ DANS LE TRAITEMENT DU CANCER DU POUMON NON À PETITES CELLULES
Applicants **
NOVARTIS AG
Inventors
BITTON, Rafael Caparica
CUI, Xiaoming
LOBETTI BODONI, Chiara
YOVINE, Alejandro Javier
Priority Data
63/570,545   27.03.2024   US
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting2317
EPO Filing, Examination, Granting12404
Japan Filing, Examination, Granting2399
South Korea Filing, Examination, Granting2573
USA Filing, Examination, Granting5940
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Total: 25,633
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Abstract[English] The present invention relates to a method of treating non-small cell lung cancer (NSCLC) which harbors a KRAS G12C mutation, wherein the method comprises the administration of KRAS G12C inhibitor 1-{6-[(4M)-4-(5-Chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methyl-1H-indazol-5-yl)-1H-pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl}prop-2-en-1-one (Compound A), or a pharmaceutically acceptable salt, solvate or hydrate thereof, and a therapeutically effective amount of pembrolizumab; in particular the present invention relates to a method of treating NSCLC wherein the NSCLC expresses at least 1% PD-L1 according to the tumor proportion score (TPS), more particularly the NSCLC expresses at least 50% PD-L1 according to the tumor proportion score (TPS).[French] La présente invention concerne une méthode de traitement du cancer du poumon non à petites cellules (NSCLC) qui héberge une mutation KRAS G12C. La méthode consiste à administrer un inhibiteur de KRAS G12C, 1-6-[(4M)-4-(5-chloro-6-méthyl-1H-indazol-4-yl)-5-méthyl-3-(1-méthyl-1H-indazol-5-yl)-1H-pyrazol-1-yl]-2-azaspiro[3,3]heptan-2-yl}prop-2-en-1-one (composé A), ou un sel, solvate ou hydrate pharmaceutiquement acceptable de celui-ci, et une quantité thérapeutiquement efficace de pembrolizumab. En particulier, la présente invention concerne une méthode de traitement du NSCLC, le NSCLC exprimant au moins 1 % de PD-L1 selon le score de proportion tumorale (TPS), plus particulièrement le NSCLC exprimant au moins 50 % de PD-L1 selon le score de proportion tumorale (TPS).

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