N-terminal scFv multispecific binding molecules

US12240908B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12240908-B2
Application numberUS-202217726950-A
CountryUS
Kind codeB2
Filing dateApr 22, 2022
Priority dateNov 5, 2019
Publication dateMar 4, 2025
Grant dateMar 4, 2025

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Multispecific binding molecules (MBMs) comprising an N-terminal scFv, a first Fab and a second Fab, MBM conjugates comprising the MBMs and cytotoxic or cytostatic agents, pharmaceutical compositions containing the MBMs and MBM conjugates, methods of using the MBMs, MBM conjugates and pharmaceutical compositions for treating cancer, nucleic acids encoding the MBMs, cells engineered to express the MBMs, and methods of producing MBMs.

First claim

Opening claim text (preview).

What is claimed is: 1. A trivalent multispecific binding molecule (MBM), comprising: (a) a first polypeptide chain comprising in an N-to C-terminal orientation: (i) an scFv comprising means for binding to human amyloid precursor-like protein 2 (APLP2); (ii) a linker; (iii) a first heavy chain region of a first Fab comprising means for binding to human fibroblast growth factor receptor 3 (FGFR3); and (iv) a first Fc domain; and (b) a second polypeptide chain comprising, in an N-to C-terminal orientation: (i) a second heavy chain region of a second Fab comprising means for binding to human FGFR3; and (ii) a second Fc domain capable of heterodimerizing with the first Fc domain to form an Fc heterodimer; (c) a third polypeptide chain comprising a first light chain that pairs with the first heavy chain region to form the first Fab; and (d) a fourth polypeptide chain comprising a second light chain that pairs with the second heavy chain region to form the second Fab. 2. The trivalent MBM of claim 1 , wherein the linker is at least 5 amino acids in length. 3. The trivalent MBM of claim 2 , wherein the linker is up to 40 amino acids in length. 4. The trivalent MBM of claim 3 , wherein the linker is 25 to 35 amino acids in length. 5. The trivalent MBM of claim 3 , wherein the linker is or comprises a multimer of GnS (SEQ ID NO: 61) or SGn (SEQ ID NO: 62), where n is an integer from 1 to 7. 6. The trivalent MBM of claim 5 , wherein the linker is or comprises a multimer of G4S (SEQ ID NO: 4). 7. The trivalent MBM of claim 1 , wherein the Fc domains in the Fc heterodimer comprise knob-in-hole mutations as compared to a wild type Fc domain. 8. The trivalent MBM of claim 1 , wherein at least one Fc domain in the Fc heterodimer comprises a star mutation as compared to a wild type Fc domain. 9. A composition comprising the trivalent MBM of claim 1 and an excipient. 10. The trivalent MBM of claim 1 , wherein the linker is attached to the first heavy chain region of the first Fab.

Assignees

Inventors

Classifications

  • Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title

  • Constant or Fc region; Isotype · CPC title

  • Valency · CPC title

  • Single chain antibody (scFv) · CPC title

  • Complementarity determining region [CDR] · CPC title

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What does patent US12240908B2 cover?
Multispecific binding molecules (MBMs) comprising an N-terminal scFv, a first Fab and a second Fab, MBM conjugates comprising the MBMs and cytotoxic or cytostatic agents, pharmaceutical compositions containing the MBMs and MBM conjugates, methods of using the MBMs, MBM conjugates and pharmaceutical compositions for treating cancer, nucleic acids encoding the MBMs, cells engineered to express th…
Who is the assignee on this patent?
Regeneron Pharma
What technology area does this patent fall under?
Primary CPC classification C07K16/2863. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 04 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).