IP Library Granted Patent US 12,240,908
Granted Patent B2
US 12,240,908 · App. 17/726,950 · Granted Mar 4, 2025

N-terminal scFv multispecific binding molecules

Inventors: Yang Shen (Scarsdale, NY); Ann-Hwee Lee (Ardsley, NY); Yan Yang (Mamaroneck, NY); Chia-Yang Lin (Scarsdale, NY)
Assignee: Regeneron Pharmaceuticals, Inc.
C07K16/2863C07K16/2896C07K16/40C07K2317/31C07K2317/35C07K2317/52C07K2317/522C07K2317/54C07K2317/55C07K2317/565C07K2317/622C07K2317/92
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Quick Facts
Patent No.
US 12,240,908
App. No.
17/726,950
Granted
Mar 4, 2025
Kind
B2
Abstract

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.

Claims (20)

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.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2024
From: SHEN, YANG; LEE, ANN-HWEE; YANG, YAN; LIN, CHIA-YANG
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 067372/0964 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2023
From: SHEN, YANG; LEE, ANN-HWEE; YANG, YAN; LIN, CHIA-YANG
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 064294/0205 →
Continuity (3)
Continuation PCTUS2020058798 · Nov 4, 2020
Provisional Application 62930916 · Nov 5, 2019
Related Publication 20220251220A1 · Aug 11, 2022
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