Anti-TFPI Antibody Variants with Differential Binding Across pH Range For Improved Pharmacokinetics

US2016009818A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016009818-A1
Application numberUS-201414772336-A
CountryUS
Kind codeA1
Filing dateMar 14, 2014
Priority dateMar 15, 2013
Publication dateJan 14, 2016
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Antibodies are disclosed that bind to and inhibit the anti-coagulant function of TFPI and have a lower affinity for TFPI at pH 6.0 than at pH 7.4. The lower affinity at pH 6 improves circulating half-life (T½) due to reduced target mediated clearance, a process by which an antibody/antigen complex is endocytosed and trafficked to the lysosome where both components are degraded. The lower affinity at pH 6.0 results in disruption of the complex prior to lysosome targeting and allows for re-circulation of the antibody. Specific modifications to antibody binding by histidine residue substitution are disclosed along with methods of use.

First claim

Opening claim text (preview).

1 . A therapeutic composition comprises an isolated human monoclonal IgG antibody that binds specifically to human tissue factor pathway inhibitor (TFPI) and has increased plasma half-life, wherein the antibody comprises at least one histidine substitution in a CDR region in either a human heavy chain or a human light chain and antibody binds to TFPI at pH 7.4 with at least two fold higher affinity than at pH 6.0. 2 . The isolated human antibody of claim 1 , wherein the heavy chain comprises SEQ ID NO: 5 3 . The isolated human antibody of claim 1 , wherein the heavy chain comprises SEQ ID NO: 6 4 . The isolated human antibody of claim 1 , wherein the heavy chain comprises SEQ ID NO: 7 5 . The isolated human antibody of claim 1 , wherein the heavy chain comprises SEQ ID NO: 8 6 . The isolated human antibody of claim 1 , wherein the heavy chain comprises SEQ ID NO: 9 7 . The isolated human antibody of claim 1 , wherein the heavy chain comprises SEQ ID NO: 10 8 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 11 9 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 12 10 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 13 11 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 14 12 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 15 13 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 16 14 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 17 15 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 18 16 . The isolated human antibody of claim 1 , wherein the heavy chain comprises SEQ ID NO: 10 and the histidine substitution is selected from the group consisting of Y102H, Y32H and Y100H, and combinations thereof. 17 . The isolated human antibody of claim 1 , wherein the light chain comprises SEQ ID NO: 17 and the histidine substitution is selected from the group consisting of Y31 H, F48H, S50H, Y49H, L27H, V45H, W90H and combinations thereof. 18 . The isolated monoclonal antibody of claim 1 , having at least two histidine substitutions selected from the group consisting of VL-Y31 H, VH-Y102H, VH-Y100H, VH-Y32H, VL-F48H, VL-S50H, VL-Y49H, VL-L27H, VL-V45H, VL-W90H and combinations thereof.

Assignees

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Classifications

  • Specific host cells or culture conditions, e.g. components, pH or temperature · CPC title

  • Fab or Fab' · CPC title

  • Internalization into the cell · CPC title

  • Stability, e.g. half-life, pH, temperature or enzyme-resistance · CPC title

  • characterized by aspects of specificity or valency · CPC title

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What does patent US2016009818A1 cover?
Antibodies are disclosed that bind to and inhibit the anti-coagulant function of TFPI and have a lower affinity for TFPI at pH 6.0 than at pH 7.4. The lower affinity at pH 6 improves circulating half-life (T½) due to reduced target mediated clearance, a process by which an antibody/antigen complex is endocytosed and trafficked to the lysosome where both components are degraded. The lower affini…
Who is the assignee on this patent?
Bayer Healthcare Llc
What technology area does this patent fall under?
Primary CPC classification C07K16/38. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jan 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).