Imidazo[1,2-b][1,2,4]triazines as c-met inhibitors
US-2016137650-A1 · May 19, 2016 · US
US10695340B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10695340-B2 |
| Application number | US-201916573362-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 17, 2019 |
| Priority date | Jun 25, 2015 |
| Publication date | Jun 30, 2020 |
| Grant date | Jun 30, 2020 |
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Provided are a therapeutic agent and a pharmaceutical composition exerting an excellent prophylactic or therapeutic effect on fibrosis and symptoms associated with fibrosis. The therapeutic agent for fibrosis comprises 4-[2-fluoro-4-[[[(2-phenylacetyl)amino]thioxomethyl]amino]-phenoxy]-7-methoxy-N-methyl-6-quinolinecarboxamide or a salt thereof as an active ingredient.
Opening claim text (preview).
The invention claimed is: 1. A method for treating fibrosis scleroderma, comprising: administering 4-[2-fluoro-4-[[[(2-phenylacetyl)amino]thioxomethyl]amino]-phenoxy]-7-methoxy-N-methyl-6-quinolinecarboxamide or a salt thereof to a patient. 2. The method of claim 1 , wherein the scleroderma is disseminated scleroderma. 3. The method of claim 1 , wherein the scleroderma is focal scleroderma. 4. The method of claim 1 , wherein the 4-[2-fluoro-4-[[[(2-phenylacetyl)amino]thioxomethyl]amino]-phenoxy]-7-methoxy-N-methyl-6-quinolinecarboxamide or a salt thereof is orally administered to the patient. 5. The method of claim 1 , wherein the salt is a methanesulfonate salt. 6. The method of claim 1 , wherein the salt is a monomethanesulfonate salt. 7. The method of claim 1 , wherein 0.005 to 5,000 mg of the 4-[2-fluoro-4-[[[(2-phenylacetyl)amino]thioxomethyl]amino]-phenoxy]-7-methoxy-N-methyl-6-quinolinecarboxamide or a salt thereof is administered to the patient. 8. The method of claim 1 , wherein 0.01 to 1,000 mg of the 4-[2-fluoro-4-[[[(2-phenylacetyl)amino]thioxomethyl]amino]-phenoxy]-7-methoxy-N-methyl-6-quinolinecarboxamide or a salt thereof is administered to the patient.
attached in position 4 · CPC title
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