Claims for Patent: 9,399,061
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Summary for Patent: 9,399,061
Title: | Methods for determining efficacy of TNF-.alpha. inhibitors for treatment of rheumatoid arthritis |
Abstract: | The invention provides methods, uses and compositions for the treatment of rheumatoid arthritis. The invention describes methods and uses for treating rheumatoid arthritis wherein a TNF.alpha. inhibitor, such as a human TNF.alpha. antibody, or antigen-binding portion thereof. Also described are methods for determining the efficacy of a TNF.alpha. inhibitor for treatment of rheumatoid arthritis in a subject. |
Inventor(s): | Kupper; Hartmut (Mutterstadt, DE), Kent; Jeffrey D. (Deerfield, IL), Cifaldi; Mary A. (Gurnee, IL), Perez; John L. (Doylestown, PA), Burmester; Gerd R. (Berlin, DE), Mease; Philip (Seattle, WA), Lovell; Daniel J. (Cincinnati, OH), Keystone; Edward (Toronto, CA), Kavanaugh; Arthur (San Diego, CA) |
Assignee: | ABBVIE BIOTECHNOLOGY LTD (Hamilton, BM) |
Application Number: | 11/786,442 |
Patent Claims: | 1. A method for treating an adult patient having moderate to severe active rheumatoid arthritis (RA), wherein the patient is nonresponsive to treatment with etanercept and
infliximab, the method comprising administering 40 mg of adalimumab to the patient every other week to thereby treat the moderate to severe active RA.
2. The method of claim 1, wherein treatment is assessed by an improvement in EULAR score. 3. The method of claim 1, wherein treatment is assessed by achieving an ACR20 response. 4. The method of claim 1, wherein adalimumab is administered to the patient by subcutaneous injection. 5. The method of claim 1, wherein said 40 mg adalimumab is comprised in a pre-filled syringe for subcutaneous injection. 6. The method of claim 1, wherein said 40 mg adalimumab is formulated at a concentration of 50 mg/ml. |
Details for Patent 9,399,061
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Janssen Biotech, Inc. | REMICADE | infliximab | For Injection | 103772 | 08/24/1998 | ⤷ Try a Trial | 2026-04-10 |
Immunex Corporation | ENBREL | etanercept | For Injection | 103795 | 11/02/1998 | ⤷ Try a Trial | 2026-04-10 |
Immunex Corporation | ENBREL | etanercept | For Injection | 103795 | 05/27/1999 | ⤷ Try a Trial | 2026-04-10 |
Immunex Corporation | ENBREL | etanercept | Injection | 103795 | 09/27/2004 | ⤷ Try a Trial | 2026-04-10 |
Immunex Corporation | ENBREL | etanercept | Injection | 103795 | 02/01/2007 | ⤷ Try a Trial | 2026-04-10 |
Immunex Corporation | ENBREL MINI | etanercept | Injection | 103795 | 09/14/2017 | ⤷ Try a Trial | 2026-04-10 |
Immunex Corporation | ENBREL | etanercept | Injection | 103795 | ⤷ Try a Trial | 2026-04-10 | |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |
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