US2009010920A1PendingUtilityA1
Fc Variants Having Decreased Affinity for FcyRIIb
Est. expiryMar 3, 2023(expired)· nominal 20-yr term from priority
A61P 43/00C07K 2317/92C07K 2317/56C07K 16/00C07K 16/2887C07K 2317/34C07K 2317/77C07K 2317/72A61K 2039/505C07K 2317/71C07K 16/2863C07K 2317/94C07K 2317/732C07K 16/2896C07K 2317/24C07K 16/32C07K 2317/40C07K 2317/41C07K 2317/52C07K 2317/31C07K 2317/734C07K 16/2893C07K 16/18C07K 2317/64C07K 16/30
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Claims
Abstract
The present invention relates to Fc variants having decreased affinity for FcγRIIb, methods for their generation, Fc polypeptides comprising optimized Fc variants, and methods for using optimized Fc variants.
Claims
exact text as granted — not AI-modified1 . A polypeptide comprising an Fc variant comprising at least one amino acid substitution in the Fc region of a parent polypeptide, wherein said Fc variant comprises at least one substitution at least one position selected from the group consisting of: 227, 228, 230, 231, 232, 247, 255, 262, 268, 271, 278, 283, 284, 285, 286, 290, 299, 300, 304, 305, 317, 318, 325, 328, 332, 336, and 337 wherein numbering is according to the EU index and wherein said Fc variant has decreased binding affinity to FcγRIIb relative to said parent polypeptide.
2 . The polypeptide of claim 1 wherein the Fc variant comprises at least one substitution at least one position selected from the group consisting of: 227, 228, 231, 232, 247, 255, 283, 286, 305, 318, 336, and 337.
3 . The polypeptide of claim 1 wherein said Fc variant comprises at least one substitution selected from the group consisting of: 227K, 227Y, 228G, 230Y, 231K, 231P, 232K, 232G, 247G, 255E, 262E, 268T, 268V, 268L, 268F, 268P, 271E, 271N, 271K, 271H, 271W, 278N, 278R, 278I, 278M, 283R, 283G, 284N, 285E, 285Y, 286E, 286Y, 290L, 290W, 299A, 299V, 299H, 299D, 299E, 299N, 299Q, 299K, 299R, 299L, 299F, 299M, 299Y, 299W, 299P, 299G, 300K, 300R, 300A, 300V, 300M, 300P, 300G, 304N, 304H, 305Y, 317E, 318Q, 318H, 318Y, 325I, 325Y, 325W, 325G, 328D, 328Q, 328K, 328R, 328S, 328T, 328Y, 328W, 328G, 332K, 332R, 336E, 336Y, and 337H.
4 . The polypeptide of claim 1 wherein the Fc variant comprises at least one combination of substitutions selected from the group consisting of: 239D/297D/326E/332E, 239D/241S/243H/262T/264T/297D/330Y/332E, 241 L/262I, 241 L/243L/262I/264I, 241E/243R/262E/264R, 241E/243Q/262T/264E, 241E/243Y/262T/264R, 243L/262I/264W, 244H/245A/247V, 297S/332E, 297D/332E, 297E/332E, and 328M/332E.
5 . The polypeptide of claim 1 wherein said parent polypeptide is an antibody.
6 . The polypeptide of claim 1 wherein said parent polypeptide is an Fc fusion protein.
7 . The polypeptide of claim 1 wherein said polypeptide further comprises an engineered glycoform.
8 . The polypeptide of claim 7 wherein said engineered glycoform comprises an altered level of fucosylation or bisecting oligosaccharides as compared to said parent polypeptide.
9 . A pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutically acceptable carrier.
10 . A method of treating a mammal in need of said treatment comprising administering the polypeptide of claim 1 .
11 . The polypeptide of claim 1 wherein said polypeptide is a full length antibody.
12 . The polypeptide of claim 1 wherein said polypeptide is a human antibody.
13 . The polypeptide of claim 1 wherein said polypeptide is an antibody fragment.Join the waitlist — get patent alerts
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