4-imidazopyridazin-1-yl-benzamides and 4-imidazotriazin-1-yl-benzamides as Btk inhibitors
US-9290504-B2 · Mar 22, 2016 · US
US9758524B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9758524-B2 |
| Application number | US-201615019543-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 9, 2016 |
| Priority date | Jul 19, 2011 |
| Publication date | Sep 12, 2017 |
| Grant date | Sep 12, 2017 |
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The present invention relates to 6-5 membered fused pyridine ring compounds according to Formula (I) or a pharmaceutically acceptable salt thereof or to pharmaceutical compositions comprising these compounds and to their use in therapy. In particular, the present invention relates to the use of 6-5 membered fused pyridine ring compounds according to Formula (I) in the treatment of Bruton's Tyrosine Kinase (Btk) mediated disorders.
Opening claim text (preview).
The invention claimed is: 1. A method of treating Mantle Cell Lymphoma (MCL) in a human subject, the method comprising administering to the human subject a compound which is (S)-4-(8-amino-3-(1-but-2-ynoylpyrrolidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide, having the structure: or a pharmaceutically acceptable salt thereof, in an amount effective to treat the MCL in the human subject. 2. The method of claim 1 , wherein the compound is present in a pharmaceutical composition. 3. The method of claim 2 , wherein the pharmaceutical composition comprises one or more pharmaceutically acceptable auxiliaries. 4. The method of claim 2 , wherein the pharmaceutical composition is administered to the human subject by oral administration. 5. The method of claim 3 , wherein the pharmaceutical composition is administered to the human subject by oral administration. 6. The method of claim 4 , wherein the pharmaceutical composition is a tablet. 7. The method of claim 5 , wherein the pharmaceutical composition is a tablet. 8. The method of claim 4 , wherein the pharmaceutical composition is a capsule. 9. The method of claim 5 , wherein the pharmaceutical composition is a capsule. 10. The method of claim 4 , wherein the pharmaceutical composition is a suspension. 11. The method of claim 5 , wherein the pharmaceutical composition is a suspension. 12. The method of claim 1 , wherein the amount administered to the human subject is 0.0001-25 mg per kg body weight. 13. The method of claim 1 , wherein the compound (S)-4-(8-amino-3-(1-but-2-ynoylpyrrolidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide is administered to the human subject. 14. The method of claim 1 , wherein a pharmaceutically acceptable salt of the compound (S)-4-(8-amino-3-(1-but-2-ynoylpyrrolidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide is administered to the human subject.
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