IP Library Granted Patent US 10,752,683
Granted Patent B2
US 10,752,683 · App. 16/384,031 · Granted Aug 25, 2020

Folate receptor 1 antibodies and immunoconjugates and uses thereof

Inventors: Olga Ab (Millis, MA); Daniel Tavares (Natick, MA); Lingyun Rui (Weston, MA); Gillian Payne (Waban, MA); Viktor S. Goldmakher (Newton, MA)
Assignee: ImmunoGen, Inc.
C07K16/28A61K31/537A61K31/5365A61K39/3955A61K39/39558A61K45/06A61K47/545A61K47/6803A61K47/6849A61K47/6851A61K47/6889C07K16/30C07K16/3069A61K2039/505C07H21/00C07K2317/14C07K2317/24C07K2317/31C07K2317/52C07K2317/524C07K2317/526C07K2317/53C07K2317/54C07K2317/55C07K2317/56C07K2317/565C07K2317/622C07K2317/624C07K2317/626C07K2317/71C07K2317/73C07K2317/732C07K2317/92C07K2317/94C12N5/16C12N15/62C12N15/63C12N15/70C12N15/79C12N2800/00
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Quick Facts
Patent No.
US 10,752,683
App. No.
16/384,031
Granted
Aug 25, 2020
Kind
B2
Abstract

Novel anti-cancer agents, including, but not limited to, antibodies and immunoconjugates, that bind to human folate receptor 1 are provided. Methods of using the agents, antibodies, or immunoconjugates, such as methods of inhibiting tumor growth are further provided.

Claims (41)

1. A method of treating cancer in a subject, comprising administering a therapeutically effective amount of an antibody or antigen binding fragment thereof that specifically binds human folate receptor 1 (FOLR1) to the subject, wherein the antibody or antigen binding fragment thereof comprises:

(a) a heavy chain CDR1 comprising the amino acid sequence SSFGMH (SEQ ID NO:72); a heavy chain CDR2 comprising the amino acid sequence YISSGSSTIS (SEQ ID NO:73); and a heavy chain CDR3 comprising the amino acid sequence EAYGSSMEY (SEQ ID NO:74) and

(b) a light chain CDR1 comprising the amino acid sequence RASQNINNNLH (SEQ ID NO:69); a light chain CDR2 comprising the amino acid sequence YVSQSVS (SEQ ID NO:70); and a light chain CDR3 comprising the amino acid sequence QQSNSWPHYT (SEQ ID NO:71).

2. The method of claim 1 , wherein the heavy chain CDR2 comprises the amino acid sequence YISSGSSTISYADSVKG (SEQ ID NO:85).

3. The method of claim 2 , wherein the antibody or antigen binding fragment thereof comprises a heavy chain variable domain comprising the amino acid sequence of SEQ ID NO:101 and a light chain variable domain comprising the amino acid sequence of SEQ ID NO:100.

4. The method of claim 1 wherein the antibody or antigen binding fragment thereof is a full length antibody.

5. The method of claim 1 , wherein the antibody or antigen binding fragment thereof is an antigen binding fragment, wherein the antigen binding fragment comprises a Fab, a Fab′, a F(ab′)2, a single chain Fv (scFv), a disulfide linked Fv, an IgG-CH2, a F(ab′)3, a tetrabody, a triabody, a diabody, a (scFv)2, or a scFv-Fc.

6. The method of claim 1 , wherein the antibody binds to human FOLR1 with a Kd of 1.0 nM or better.

7. The method of claim 1 , wherein the antibody binds to human FOLR1 with a Kd of about 0.06 nM to about 1.0 nM.

8. The method of claim 1 , wherein the cancer is selected from the group consisting of ovarian cancer, breast cancer, uterine cancer, pancreatic cancer, renal cancer, peritoneal cancer, and lung cancer.

9. The method of claim 1 , wherein the cancer is endometrial cancer.

10. A method of treating cancer in a subject, comprising administering a therapeutically effective amount of an immunoconjugate having the formula (A)-(L)-(C) to the subject, wherein:

(A) is the antibody or antigen binding fragment thereof of claim 1 ;

(L) is a linker; and

(C) is a cytotoxic agent;

wherein (L) links (A) to (C).

11. The method of claim 10 , wherein the linker is a cleavable linker.

12. The method of claim 10 , wherein the linker is a non-cleavable linker.

13. The method of claim 10 , wherein the linker is a hydrophilic linker or a dicarboxylic acid based linker.

14. The method of claim 10 , wherein the linker is selected from the group consisting: N-succinimidyl 4-(2-pyridyldithio)pentanoate (SPP) or N-succinimidyl 4-(2-pyridyldithio)-2-sulfopentanoate (sulfo-SPP); N-succinimidyl 4-(2-pyridyldithio)butanoate (SPDB) or N-succinimidyl 4-(2-pyridyldithio)-2-sulfobutanoate (sulfo-SPDB); N-succinimidyl 4-(maleimidomethyl) cyclohexanecarboxylate (SMCC); N-sulfosuccinimidyl 4-(maleimidomethyl) cyclohexanecarboxylate (sulfoSMCC); N-succinimidyl-4-(iodoacetyl)-aminobenzoate (SIAB); and N-succinimidyl-[(N-maleimidopropionamido)-tetraethyleneglycol] ester (NHS-PEG4-maleimide).

15. The method of claim 10 , wherein the cytotoxic agent is selected from the group consisting of a maytansinoid, benzodiazepine, taxoid, CC-1065, duocarmycin, calicheamicin, dolastatin, auristatin, tomaymycin and leptomycin or a prodrug of the agent.

16. The method of claim 15 , wherein the maytansinoid is N(2′)-deacetyl-N(2′)-(3-mercapto-1-oxopropyl)-maytansine (DM1) or N(2′)-deacetyl-N(2′)-(4-mercapto-4-methyl-1-oxopentyl)-maytansine (DM4).

17. The method of claim 10 , wherein (L) is sulfo-SPDB and (C) is DM4.

18. The method of claim 10 , wherein the immunoconjugate comprises 2-6 (C) or 3-4 (C).

19. The method of claim 10 , wherein the cancer is selected from the group consisting of ovarian cancer, breast cancer, uterine cancer, pancreatic cancer, renal cancer, peritoneal cancer, and lung cancer.

20. The method of claim 10 , wherein the cancer is endometrial cancer.

21. A method of treating cancer in a subject, comprising administering a therapeutically effective amount of an immunoconjugate having the formula (A)-(L)-(C) to the subject, wherein:

(A) is the antibody or antigen binding fragment thereof of claim 3 ;

(L) is a linker; and

(C) is a cytotoxic agent;

wherein (L) links (A) to (C).

22. The method of claim 21 , wherein the linker is a cleavable linker.

23. The method of claim 21 , wherein the linker is a non-cleavable linker.

24. The method of claim 21 , wherein the linker is a hydrophilic linker or a dicarboxylic acid based linker.

25. The method of claim 21 , wherein the linker is selected from the group consisting: N-succinimidyl 4-(2-pyridyldithio)pentanoate (SPP) or N-succinimidyl 4-(2-pyridyldithio)-2-sulfopentanoate (sulfo-SPP); N-succinimidyl 4-(2-pyridyldithio)butanoate (SPDB) or N-succinimidyl 4-(2-pyridyldithio)-2-sulfobutanoate (sulfo-SPDB); N-succinimidyl 4-(maleimidomethyl) cyclohexanecarboxylate (SMCC); N-sulfosuccinimidyl 4-(maleimidomethyl) cyclohexanecarboxylate (sulfoSMCC); N-succinimidyl-4-(iodoacetyl)-aminobenzoate (SIAB); and N-succinimidyl-[(N-maleimidopropionamido)-tetraethyleneglycol] ester (NHS-PEG4-maleimide).

26. The method of claim 21 , wherein the cytotoxic agent is selected from the group consisting of a maytansinoid, benzodiazepine, taxoid, CC-1065, duocarmycin, calicheamicin, dolastatin, auristatin, tomaymycin and leptomycin or a prodrug of the agent.

27. The method of claim 26 , wherein the maytansinoid is N(2′)-deacetyl-N(2′)-(3-mercapto-1-oxopropyl)-maytansine (DM1) or N(2′)-deacetyl-N(2′)-(4-mercapto-4-methyl-1-oxopentyl)-maytansine (DM4).

28. The method of claim 21 , wherein (L) is sulfo-SPDB and (C) is DM4.

29. The method of claim 21 , wherein the immunoconjugate comprises 2-6 (C) or 3-4 (C).

30. The method of claim 21 , wherein the cancer is selected from the group consisting of ovarian cancer, breast cancer, uterine cancer, pancreatic cancer, renal cancer, peritoneal cancer, and lung cancer.

31. The method of claim 21 , wherein the cancer is endometrial cancer.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Feb 12, 2024
From: BIOPHARMA CREDIT PLC
To: IMMUNOGEN, INC.; IMMUNOGEN SWITZERLAND GMBH
Reel/Frame 066553/0109 →
PATENT SECURITY AGREEMENT Recorded Apr 6, 2023
From: IMMUNOGEN, INC.; IMMUNOGEN SWITZERLAND GMBH
To: BIOPHARMA CREDIT PLC
Reel/Frame 063282/0894 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2019
From: AB, OLGA; TAVARES, DANIEL; RUI, LINGYUN; PAYNE, GILLIAN; GOLDMAKHER, VIKTOR S.
To: IMMUNOGEN, INC.
Reel/Frame 048927/0219 →
Continuity (8)
Division 15583281 · May 1, 2017
Division 14813209 · Aug 5, 2015
Division 13800835 · Mar 13, 2013
Division 13033723 · Feb 24, 2011
Provisional Application 61307797 · Feb 24, 2010
Provisional Application 61346595 · May 20, 2010
Provisional Application 61413172 · Nov 12, 2010
Related Publication 20190345248A1 · Nov 14, 2019
Cited By (12)
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