US2018201674A1PendingUtilityA1
Methods of Using IL-1beta Compounds
Est. expiryOct 26, 2025(expired)· nominal 20-yr term from priority
A61P 9/10A61P 43/00A61P 37/06A61P 9/00A61P 37/02A61P 35/00A61P 37/00A61P 25/28A61P 29/00A61P 25/00A61P 1/04A61P 21/00A61P 11/00A61P 1/00A61P 19/00A61P 19/02A61K 38/20C07K 2317/92C07K 2317/76A61K 2039/505C07K 2317/21C07K 16/245C07K 2317/565C07K 2317/56A61K 38/16A61K 39/3955C07K 16/246
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Claims
Abstract
This invention relates to methods employing IL-1 beta-ligand/IL-1 receptor disrupting compounds, such as IL-1 beta antibodies or IL-1 receptor antibodies, in the treatment and/or prevention of auto-inflammatory syndromes in mammals, particularly humans.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treating an auto-inflammatory syndrome in a patient in need thereof, comprising administering to a patient in need thereof an effective amount of an IL-1beta antibody comprising:
a) an immunoglobulin heavy chain variable domain (V H ) comprising the amino acid sequence set forth as SEQ ID NO:1; b) an immunoglobulin light chain variable domain (V L ) comprising the amino acid sequence set forth as SEQ ID NO:2; c) an immunoglobulin V H comprising the amino acid sequence set forth as SEQ ID NO: 1 and an immunoglobulin V L comprising the amino acid sequence set forth as SEQ ID NO: 2; or d) the three CDRs of the V H as set forth as SEQ ID NO:1 and the three CDRs of the V L as set forth as SEQ ID NO:2.
2 . The method according to claim 1 , wherein the IL-1beta antibody comprises
a) an immunoglobulin V H comprising the amino acid sequence set forth as SEQ ID NO: 1 and an immunoglobulin V L comprising the amino acid sequence set forth as SEQ ID NO: 2; or b) the three CDRs of the V H as set forth as SEQ ID NO:1 and the three CDRs of the V L as set forth as SEQ ID NO:2.
3 . The method according to claim 2 , wherein the three CDRs of SEQ ID NO:1 comprise the amino acid sequences set forth as SEQ ID NOs:3-5, and wherein the three CDRs of SEQ ID NO:2 comprise the amino acid sequences set forth as SEQ ID NOs:6-8.
4 . The method according to claim 2 , wherein the IL-1beta antibody comprises an antigen binding site comprising at least one immunoglobulin V H which comprises in sequence hypervariable regions CDR1, CDR2 and CDR3, said CDR1 having the amino acid sequence Val-Tyr-Gly-Met-Asn (SEQ ID NO:3), said CDR2 having the amino acid sequence Ile-Ile-Trp-Tyr-Asp-Gly-Asp-Asn-Gln-Tyr-Tyr-Ala-Asp-Ser-Val-Lys-Gly (SEQ ID NO:4), and said CDR3 having the amino acid sequence Asp-Leu-Arg-Thr-Gly-Pro (SEQ ID NO:5) and an antigen binding site comprising at least one immunoglobulin V L which comprises in sequence hypervariable regions CDR1′, CDR2′ and CDR3′, said CDR1′ having the amino acid sequence Arg-Ala-Ser-Gln-Ser-Ile-Gly-Ser-Ser-Leu-His (SEQ ID NO:6) said CDR2′ having the amino acid sequence Ala-Ser-Gln-Ser-Phe-Ser (SEQ ID NO:7) and said CDR3′ having the amino acid sequence His-Gln-Ser-Ser-Ser-Leu-Pro (SEQ ID NO:8).
5 . The method of claim 4 , wherein the IL-1beta antibody is a human antibody.
6 . The method of claim 5 , wherein the IL-1beta antibody is administered once every week or less frequently.
7 . The method of claim 6 , wherein the IL-1beta antibody is administered to the patient subcutaneously.
8 . The method of claim 5 , wherein the IL-1beta antibody is administered once every month or less frequently.
9 . The method of claim 5 , wherein the IL-1beta antibody is administered once every two months or less frequently.
10 . The method of claim 5 , wherein the IL-1beta antibody is administered once every three months or less frequently.
11 . The method of claim 5 , wherein the IL-1beta antibody is administered once every four months or less frequently.
12 . The method of claim 1 , wherein the IL-1beta antibody is ACZ885.
13 . The method of claim 2 , wherein the IL-1beta antibody is ACZ885.
14 . The method of claim 3 , wherein the IL-1beta antibody is ACZ885.
15 . The method of claim 4 , wherein the IL-1beta antibody is ACZ885.
16 . The method of claim 5 , wherein the IL-1beta antibody is ACZ885.
17 . The method of claim 6 , wherein the IL-1beta antibody is ACZ885.
18 . The method of claim 7 , wherein the IL-1beta antibody is ACZ885.
19 . The method of claim 8 , wherein the IL-1beta antibody is ACZ885.
20 . The method of claim 9 , wherein the IL-1beta antibody is ACZ885.Cited by (0)
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