Substituted 2,3-dihydroimidazo[1,2-C]quinazoline-containing combinations

US10406162B2 · kind B2 · utility

Assignee

• Bayer Pharma Aktiengesellschaft · DE

Inventors

• Ningshu Liu · Berlin, DE
• Carol Pena · New Haven, US
• Michael F. Jeffers · Flourtown, US
• Isabelle Genvresse · Berlin, DE

Key dates

• Filing date: Mar 7, 2016
• Grant date: Sep 10, 2019
• Expiry date: Mar 7, 2036

Classification

• Technology area (CPC C): Chemistry; Metallurgy
• CPC primary: C12Q2600/158
• WIPO field: Pharmaceuticals
• WIPO sector: Chemistry

Abstract

The present invention relates to * combinations of: ⋅ component A: one or more 2,3-dihydroimidazo[1,2-c]quinazoline compounds of general formula (A1) or (A2), or a physiologically acceptable salt, solvate, hydrate or ⋅ stereoisomer thereof; ⋅ component B: one or more substituted 5-(1-benzothiophen-2-yl)pyrrolo[2,1-f][1,2,4]-triazin-4-amine compounds of general formula (B), or a physiologically acceptable salt, solvate, hydrate or stereoisomer thereof; ⋅ in which optionally some or all of the components are in the form of a pharmaceutical formulation which is ready for use to be administered simultaneously, concurrently, separately or sequentially, ⋅ dependently of one another by the oral, intravenous, topical, local installations, ⋅ intraperitoneal or nasal route; * use of such combinations for the preparation of a medicament for the treatment or prophylaxis of a cancer; * a kit comprising such a combination; * use of biomarkers which is the loss of tumor suppressor PTEN or FBXW7, for predicting the sensitivity and/or resistance of a cancer patient to said compound and providing a rationale-based dosage to increase sensitivity and/or to overcome resistance; * a method of determinin…