CA3016092C — Egfr inhibitor free base or acid salt polycrystalline form, preparation method therefor, and application
Assigned to Jiangsu Hansoh Pharmaceutical Group Co Ltd · Expires 2025-03-11 · 1y expired
What this patent protects
Disclosed are an EGFR inhibitor free base or acid salt polycrystalline form, a preparation method therefor, and an application. The present invention specifically relates to an N-(5-((4-(l-cyclopropyl-lH-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4…
USPTO Abstract
Disclosed are an EGFR inhibitor free base or acid salt polycrystalline form, a preparation method therefor, and an application. The present invention specifically relates to an N-(5-((4-(l-cyclopropyl-lH-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxyphenyl)acrylamide free base or acid salt polycrystalline form, a preparation method therefor, and an application of the polycrystalline form in preparing a drug treating an EGFR mutant activity-mediated disease. The present invention is used for inhibiting the activity of an L858R EGFR mutant, a T790M EGFR mutant and an exon 19 deletion activating mutant etc., may be widely applied in the preventing and treating cancer, especially non-small cell lung cancer and other related diseases, and is expected to develop into a new generation of EGFR inhibitors.
Drugs covered by this patent
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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