US2020231667A1PendingUtilityA1
Novel compounds capable of antagonizing islet amyloid polypeptide (iapp) induced beta-cell damage and impaired glucose tolerance
Est. expiryMar 12, 2034(~7.7 yrs left)· nominal 20-yr term from priority
C07K 2317/24A01K 2267/0362A01K 67/0275A61K 2039/505C07K 2317/21A01K 2217/052A01K 2267/0312C07K 2317/33A61K 39/395A01K 2227/105C07K 16/18C07K 16/26A61K 45/06A61P 3/10C07K 2317/565C07K 2317/76A61K 39/3955A61K 49/0008A61K 47/6847C07K 2317/56
60
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Claims
Abstract
Described are molecules specifically binding to human islet amyloid polypeptide (hIAPP) also known as amylin, particularly human-derived antibodies as well as fragments, derivatives and variants thereof for antagonizing islet amyloid polypeptide (IAPP) induced β-cell damage and impaired glucose tolerance winch are symptoms typically associated with diabetes mellitus type 2 (T2D).
Claims
exact text as granted — not AI-modified1 - 19 . (canceled)
20 . An antibody or a human islet amyloid polypeptide (hIAPP)-binding fragment thereof, wherein the antibody or the hIAPP-binding fragment thereof comprises an hIAPP-binding domain comprising:
(i) a heavy chain variable (VH) region comprising the three complementarity determining regions (CDRs) of the heavy chain variable (VH) sequence of SEQ ID NO: 2 (as depicted in FIG. 1 ); and (ii) a light chain variable (VL) region comprising the amino acid sequence of SEQ ID NO: 6.
21 . The antibody or hIAPP-binding fragment thereof of claim 20 , wherein the VH region comprises the amino acid sequence of SEQ ID NO: 2.
22 . The antibody or hIAPP-binding fragment thereof of claim 20 , wherein the antibody or hIAPP-binding fragment thereof comprises a polypeptide sequence which is heterologous to the hIAPP-binding domain.
23 . The antibody or hIAPP-binding fragment thereof of claim 20 , wherein the antibody or hIAPP-binding fragment thereof comprises a constant domain or part thereof which is heterologous to the hIAPP-binding domain.
24 . The antibody or hIAPP-binding fragment thereof of claim 23 , wherein the constant domain is of the IgG type.
25 . The antibody or hIAPP-binding fragment thereof of claim 24 , wherein the constant domain is of the IgG1 class or isotype.
26 . The antibody or hIAPP-binding fragment thereof of claim 23 , wherein the constant domain is a human constant domain.
27 . The antibody or hIAPP-binding fragment thereof of claim 20 , wherein the antibody or hIAPP-binding fragment thereof is (a) detectably labeled or (b) attached to a drug.
28 . The antibody or hIAPP-binding fragment thereof of claim 27 , wherein the detectable label is selected from the group consisting of an enzyme, a radioisotope, a fluorophore, and a heavy metal.
29 . The antibody or hIAPP-binding fragment thereof of claim 20 , wherein the antibody or hIAPP-binding fragment thereof selectively binds aggregated hIAPP in pancreas tissue of a human diabetic subject.
30 . The antibody or hIAPP-binding fragment thereof of claim 20 , wherein the antibody is a human-derived monoclonal antibody.
31 . A pharmaceutical composition comprising the antibody or hIAPP-binding fragment thereof of claim 20 .
32 . The pharmaceutical composition of claim 31 , wherein the composition further comprises an agent capable of preventing or reducing IAPP amyloid formation.
33 . The pharmaceutical composition of claim 32 , wherein the agent is selected from the group consisting of flavonoids, IAPP analogs, metformin, and thiazolidinediones
34 . The pharmaceutical composition of claim 33 , wherein the thiazolidinedione is rosiglitazone.
35 . The pharmaceutical composition of claim 31 , further comprising a pharmaceutically acceptable carrier or diluent.
36 . A method of protecting β-cells from hIAPP induced cell damage and/or islet amyloid toxic effects, the method comprising administering a therapeutically effective amount of an antibody or hIAPP-binding fragment thereof of claim 20 to a subject in need thereof.
37 . A polynucleotide encoding the antibody or hIAPP-binding fragment thereof of claim 1 .
38 . A cDNA encoding the antibody or hIAPP-binding fragment thereof of claim 1 .Cited by (0)
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