US2014017236A1PendingUtilityA1
Methods for treating interleukin-6 related diseases
Assignee: CHUGAI PHARMACEUTICAL CO LTDPriority: Apr 28, 2003Filed: Sep 13, 2013Published: Jan 16, 2014
Est. expiryApr 28, 2023(expired)· nominal 20-yr term from priority
A61P 29/00A61P 19/02A61K 2039/505A61K 31/519A61K 39/395C07K 16/2803A61K 45/06A61K 39/39533A61K 39/3955C07K 16/2866A61K 2039/545
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Claims
Abstract
A pharmaceutical composition for the treatment of interleukin-6 (IL-6) related diseases, comprising an interleukin-6 antagonist (IL-6 antagonist) and immunosuppressants. The IL-6 antagonist is preferably an antibody to an interleukin-6 receptor (IL-6R).
Claims
exact text as granted — not AI-modified1 . A method for treating rheumatoid arthritis (RA) in a patient comprising administering 4 mg/kg or 8 mg/kg of a humanized anti-human interleukin-6 receptor (anti-IL-6R) antibody to the RA patient every four weeks.
2 . The method of claim 1 wherein 4 mg/kg of the anti-IL6R antibody is administered every four weeks.
3 . The method of claim 1 wherein 8 mg/kg of the anti-IL6R antibody is administered every four weeks.
4 . The method of claim 1 wherein the anti-IL6R antibody is administered to the RA patient as a monotherapy.
5 . The method of claim 1 further comprising administering methotrexate to the RA patient.
6 . The method of claim 1 which improves American College of Rheumatology (ACR) response in the RA patient, wherein the ACR response is selected from the group consisting of ACR20, ACR50, and ACR70.
7 . The method of claim 6 wherein the ACR response is ACR20 response.
8 . The method of claim 6 wherein the ACR response is ACR50 response.
9 . The method of claim 6 wherein the ACR response is ACR70 response.
10 . The method of claim 1 wherein the anti-IL-6R antibody is MRA antibody.
11 . The method of claim 10 wherein 8 mg/kg of the MRA antibody is administered every four weeks.
12 . The method of claim 11 wherein the 8 mg/kg dose results in less anti-MRA antibody than a 4 mg/kg dose.Join the waitlist — get patent alerts
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