Claims for Patent: 9,987,272
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Summary for Patent: 9,987,272
Title: | Compound useful for the treatement of degenerative and inflammatory diseases |
Abstract: | A pyrazolopyridine compound according to Formula I, able to inhibit JAK is disclosed, as well as pharmaceutically acceptable salts, a solvate thereof, solvates of the pharmaceutically acceptable salts and biologically active metabolites thereof. The compound may be prepared as a pharmaceutical composition, and may be used for the treatment or prophylaxis of a variety of conditions in mammals including humans, and particularly, such conditions as may be associated with aberrant JAK activity, including by way of non-limiting example, allergy, inflammatory conditions, autoimmune diseases, proliferative diseases, transplant rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6. ##STR00001## |
Inventor(s): | Menet; Christel Jeanne Marie (Mechelen, BE), Hodges; Alastair James (Essex, GB), Vater; Huw David (Essex, GB) |
Assignee: | GALAPAGOS NV (Mechelen, BE) |
Application Number: | 15/005,442 |
Patent Claims: | 1. A method for the treatment of Crohn's Disease, comprising administering an amount of a compound according to Formula I: ##STR00006## or pharmaceutically acceptable salt
thereof, sufficient to effect said treatment.
2. The method according to claim 1, wherein the compound or pharmaceutically acceptable salt thereof, is administered in combination with a further therapeutic agent for the treatment of Crohn's Disease. 3. A method for the treatment of Crohn's Disease, comprising administering an amount of the pharmaceutical composition comprising a pharmaceutically acceptable carrier and an amount of a compound according to Formula I: ##STR00007## or a pharmaceutically acceptable salt thereof, sufficient to effect said treatment. 4. The method according to claim 3, wherein said compound is administered in combination with one or more further therapeutic agents selected from Crohn's Disease treatment agents. 5. The method according to claim 3, wherein said compound is administered in combination with one further therapeutic agent selected from Crohn's Disease treatment agents. 6. The method according to claim 2, wherein the further therapeutic agent is an agent selected from glucocorticoids, synthetic disease modifying immunomodulatory agents, and biological disease modifying immunomodulatory agents. 7. The method according to claim 4, wherein the further therapeutic agent is an agent selected glucocorticoids, synthetic disease modifying immunomodulatory agents, and biological disease modifying immunomodulatory agents. 8. The method according to claim 5, wherein the further therapeutic agent is an agent selected from glucocorticoids, synthetic disease modifying immunomodulatory agents, and biological disease modifying immunomodulatory agents. 9. The method according to claim 6, wherein the further therapeutic agent is an agent selected from prednisone, budesonide, methotrexate, leflunomide, sulfasalazine, mesalazine, azathioprine, 6-mercaptopurine, cyclosporin, infliximab, adalimumab, rituximab, and abatacept. 10. The method according to claim 7, wherein the further therapeutic agent is an agent selected from prednisone, budesonide, methotrexate, leflunomide, sulfasalazine, mesalazine, azathioprine, 6-mercaptopurine, cyclosporin, infliximab, adalimumab, rituximab, and abatacept. 11. The method according to claim 8, wherein the further therapeutic agent is an agent selected from prednisone, budesonide, methotrexate, leflunomide, sulfasalazine, mesalazine, azathioprine, 6-mercaptopurine, cyclosporin, infliximab, adalimumab, rituximab, and abatacept. |
Details for Patent 9,987,272
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Genentech, Inc. | RITUXAN | rituximab | Injection | 103705 | 11/26/1997 | ⤷ Try a Trial | 2031-04-28 |
Janssen Biotech, Inc. | REMICADE | infliximab | For Injection | 103772 | 08/24/1998 | ⤷ Try a Trial | 2031-04-28 |
Abbvie Inc. | HUMIRA | adalimumab | Injection | 125057 | 12/31/2002 | ⤷ Try a Trial | 2031-04-28 |
Abbvie Inc. | HUMIRA | adalimumab | Injection | 125057 | 02/21/2008 | ⤷ Try a Trial | 2031-04-28 |
Abbvie Inc. | HUMIRA | adalimumab | Injection | 125057 | 04/24/2013 | ⤷ Try a Trial | 2031-04-28 |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |
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