IP Library Granted Patent US 11,591,398
Granted Patent B2
US 11,591,398 · App. 16/475,597 · Granted Feb 28, 2023

Single domain antibodies to programmed cell death protein 1 (PD-1)

Inventors: Phil Hayes (Cambridge, GB); James Legg (Cambridge, GB); Martyna Lewandowska (Cambridge, GB); Colette Johnston (Cambridge, GB); Brian McGuinness (Cambridge, GB); Mike Romanos (Cambridge, GB); Christine Rossant (Cambridge, GB); Yumin Teng (Cambridge, GB)
Assignee: CRESCENDO BIOLOGICS LIMITED
C07K16/2818A01K67/0278A61P35/00C07K16/2803C12N15/85G01N33/6803A01K2227/105A61K2039/505C07K16/18C07K2317/24C07K2317/31C07K2317/33C07K2317/35C07K2317/565C07K2317/569C07K2317/70C07K2317/76C07K2317/92C07K2317/94C07K2319/00
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Quick Facts
Patent No.
US 11,591,398
App. No.
16/475,597
Granted
Feb 28, 2023
Kind
B2
Abstract

The invention relates to PD-1 binding agents that block the interaction of PD-1 with its ligands, and the use of such binding agents in the treatment, prevention and detection of disease.

Claims (17)

1. An isolated V H single domain antibody that binds to human programmed cell death 1 protein (PD-1) and blocks the interaction of PD-1 and PD-L1, comprising three complementarity determining regions CDR1, CDR2 and CDR3, wherein the CDR1 sequence comprises SEQ ID NO:438, the CDR2 sequence comprises SEQ ID NO:439, and the CDR3 sequence comprises SEQ ID NO:440.

2. The isolated V H single domain antibody of claim 1 , comprising SEQ ID NO:441.

3. The isolated V H single domain antibody of claim 1 , comprising a sequence with at least 70% homology to SEQ ID NO:441.

4. The isolated V H single domain antibody of claim 1 , comprising a sequence with at least 80% homology to SEQ ID NO:441.

5. The isolated V H single domain antibody of claim 1 , comprising a sequence with at least 90% homology to SEQ ID NO:441.

6. The isolated V H single domain antibody of claim 1 , wherein said single domain antibody is conjugated to a single domain antibody that binds to human serum albumin.

7. The isolated V H single domain antibody of claim 1 obtained or obtainable from a transgenic rodent that expresses a transgene comprising human V, D and J regions, optionally wherein said rodent does not produce any functional endogenous light and heavy chains.

8. An isolated binding agent comprising the single domain antibody of claim 1 .

9. The isolated binding agent of claim 8 , wherein said single domain antibody is linked to a second antibody or an antibody fragment, wherein said second antibody or antibody fragment binds to and is an inhibitor of an immune checkpoint molecule selected from the group consisting of PD-L1, PD-L2, CTLA-4, TIM-3, LAG-3, CEACAM, VISTA, BTLA, TIGIT, LAIR1, CD160, 2B4 and TGFR beta.

10. The isolated binding agent of claim 9 , wherein the immune checkpoint molecule is LAG-3.

11. The isolated binding agent of claim 8 , wherein said single domain antibody is linked to a second antibody or an antibody fragment, wherein said second antibody or antibody fragment binds to and is an activator of a costimulatory molecule selected from the group consisting of an agonist of one or more of IL 2, IL-12, OX40, OX4OL, CD2, CD3, CD27, ICAM-1, LFA-1, CD11a, CD18, ICOS (CD278), 4-1 BB (CD137), GITR, CD30, CD40, BAFFR, HVEM, CD7, LIGHT, NKG2C, SLAMF7, NKp80, CD160, B7-H3, B7-H4 or CD83 ligand, CD8, CD28, CD4 and ICAM-1.

12. An immunoconjugate comprising the single domain antibody of claim 1 linked to a therapeutic agent, optionally wherein said therapeutic agent is a toxin, enzyme, radioisotope or other chemical moiety.

13. A pharmaceutical composition comprising the single domain antibody of claim 1 and a pharmaceutical carrier.

14. A kit comprising the single domain antibody of claim 1 .

15. A bispecific molecule comprising the single domain antibody of claim 1 linked to a second functional moiety having a different binding specificity than said single domain antibody, wherein said second moiety is an antibody or an antibody fragment, wherein said second moiety binds to and is an inhibitor of an immune checkpoint molecule selected from the group consisting of PD-L1, PD-L2, CTLA-4, TIM-3, LAG-3, CEACAM, VISTA, BTLA, TIGIT, LAIR1, CD160, 2B4 and TGFR beta.

16. The bispecific molecule of claim 15 , wherein the immune checkpoint molecule is LAG-3.

17. A bispecific molecule comprising the single domain antibody of claim 1 linked to a second functional moiety having a different binding specificity than said single domain antibody, wherein said second moiety is an antibody or an antibody fragment that binds to a costimulatory molecule selected from the group consisting of IL 2, IL-12, OX40, OX4OL, CD2, CD3, CD27, ICAM-1, LFA-1, CD11a, CD18, ICOS (CD278), 4-1 BB (CD137), GITR, CD30, CD40, BAFFR, HVEM, CD7, LIGHT, NKG2C, SLAMF7, NKp80, CD160, B7-H3, B7-H4 or CD83 ligand, CD8, CD28, CD4 and ICAM-1.

Assignments (3)
REDACTED RELEASE OF SECURITY INTEREST Recorded Sep 6, 2024
From: KREOS CAPITAL VII (UK) LIMITED
To: CRESCENDO BIOLOGICS LIMITED
Reel/Frame 068859/0042 →
SECURITY INTEREST Recorded Jul 24, 2023
From: CRESCENDO BIOLOGICS LIMITED
To: KREOS CAPITAL VII (UK) LIMITED
Reel/Frame 064351/0761 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2020
From: HAYES, PHIL; LEGG, JAMES; LEWANDOWSKA, MARTYNA; JOHNSTON, COLETTE; MCGUINNESS, BRIAN; ROMANOS, MIKE; ROSSANT, CHRISTINE; TENG, YUMIN
To: CRESCENDO BIOLOGICS LIMITED
Reel/Frame 053230/0568 →
Priority Claims (3)
GB 1700207 · Jan 6, 2017 · national
GB 1700208 · Jan 6, 2017 · national
GB 1700210 · Jan 6, 2017 · national
Continuity (1)
Related Publication 20200239573A1 · Jul 30, 2020