EP3628664A1 — Irreversible inhibitors of kras g12c mutant
Assigned to Max Planck Gesellschaft zur Foerderung der Wissenschaften eV · Expires 2020-04-01 · 6y expired
What this patent protects
The present invention relates to novel substituted 2-halopyrimidines and 5-halopyrazines, as well as pharmaceutical compositions containing at least one of these substituted 2-halopyrimidines or 5-halopyrazines together with at least one pharmaceutically acceptable carrier, excip…
USPTO Abstract
The present invention relates to novel substituted 2-halopyrimidines and 5-halopyrazines, as well as pharmaceutical compositions containing at least one of these substituted 2-halopyrimidines or 5-halopyrazines together with at least one pharmaceutically acceptable carrier, excipient and/or diluent. Said substituted 2-halopyrimidines and 5-halopyrazines are covalently binding to KRas mutant G12C and therefore, are useful for the prophylaxis and treatment of cancer by direct inhibition of the KRas G12C-oncogenic signaling in cells.
Drugs covered by this patent
- Krazati (ADAGRASIB) · Bristol-Myers Squibb
Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.
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