Anti-CD79B antibodies and immunoconjugates and methods of use

Patent metadata

Field	Value
Publication number	US-9896506-B2
Application number	US-201514734957-A
Country	US
Kind code	B2
Filing date	Jun 9, 2015
Priority date	Jan 31, 2008
Publication date	Feb 20, 2018
Grant date	Feb 20, 2018

Abstract

The present invention is directed to compositions of matter useful for the treatment of hematopoietic tumor in mammals, including immunoconjugates comprising anti-CD79b cysteine-engineered antibody huMA79b.v28, and to methods of using those compositions of matter for the same.

First claim

What is claimed is:

1. An immunoconjugate comprising an anti-CD79b cysteine engineered antibody, wherein the antibody comprises a heavy chain and a light chain,
wherein the light chain comprises
(i) an HVR-L1 sequence of KASQSVDYEGDSFLN (SEQ ID NO: 194);
(ii) an HVR-L2 sequence of AASNLES (SEQ ID NO: 195); and
(iii) an HVR-L3 sequence of QQSNEDPLT (SEQ ID NO: 196);
wherein the heavy chain comprises
(i) an HVR-H1 sequence of GYTFSSYWIE (SEQ ID NO: 202);
(ii) an HVR-H2 sequence of GEILPGGGDTNYNEIFKG (SEQ ID NO: 203); and
(iii) an HVR-H3 sequence of TRRVPIRLDY (SEQ ID NO: 204), and
wherein the antibody comprises an engineered cysteine at position 118 of the heavy chain according to EU numbering convention, and wherein the anti-CD79b cysteine engineered antibody is covalently attached to a cytotoxic agent through the engineered cysteine.

2. The immunoconjugate according to claim 1 , wherein the cytotoxic agent is selected from the group consisting of a chemotherapeutic agent, a growth inhibitory agent, a toxin, a drug moiety, an antibiotic, a nucleolytic enzyme and a radioactive isotope.

3. The immunoconjugate of claim 1 having Formula I:
Ab-(L-D) p   I

wherein Ab is the anti-CD79b cysteine engineered antibody, D is the cytotoxic agent and the cytotoxic agent is a drug moiety, L is a linker moiety which links the Ab to D through the engineered cysteine, and p is 1, 2, 3, or 4.

4. The immunoconjugate of claim 3 wherein L has the formula:
—A a —W w —Y y —

where:
A is a Stretcher unit covalently attached to a cysteine thiol of the engineered cysteine;
a is 0 or 1;
each W is independently an Amino Acid unit;
w is an integer ranging from 0 to 12;
Y is a Spacer unit covalently attached to the drug moiety; and
y is 0, 1 or 2.

5. The immunoconjugate of claim 4 having the formula:

where PAB is para-aminobenzylcarbamoyl, and R 17 is a divalent radical selected from (CH 2 ) r , C 3 -C 8 carbocyclyl, O—(CH 2 ) r , arylene, (CH 2 ) r -arylene, -arylene-(CH 2 ) r —, (CH 2 ) r —(C 3 -C 8 carbocyclyl), (C 3 -C 8 carbocyclyl)-(CH 2 ), C 3 -C 8 heterocyclyl, (CH 2 ) r —(C 3 -C 8 heterocyclyl), —C 3 -C 8 heterocyclyl)-(CH 2 ) r —, —(CH 2 ) r C(O)NR b (CH 2 ) r —, —(CH 2 CH 2 O) r —, —(CH 2 CH 2 O) r —CH 2 , —(CH 2 ) r C(O)NR b (CH 2 CH 2 O) r —, —(CH 2 ) r C(O)NR b (CH 2 CH 2 O) r —CH 2 —, —(CH 2 CH 2 O) r C(O)NR b (CH 2 CH 2 O) r —, —(CH 2 CH 2 O) r C(O)NR b (CH 2 CH 2 O) r —CH 2 —, and —(CH 2 CH 2 O) r C(O)NR b (CH 2 ) r —; where R b is H, C 1 -C 6 alkyl, phenyl, or benzyl; and r is independently an integer ranging from 1 to 10.

6. The immunoconjugate of claim 5 wherein W w is valine-citrulline.

7. The immunoconjugate of claim 6 wherein R 17 is (CH 2 ) 5 or (CH 2 ) 2 .

8. The immunoconjugate of claim 3 having the formula:

9. The immunoconjugate of claim 3 wherein L comprises 4-((2,5-dioxopyrrolidin-1-yl)methyl)cyclohexanecarboxylic acid (SMCC), 4-mercaptopentanoic acid (SPP), 4-mercaptobutanoic acid (SPDB), 6-maleimidocaproyl (MC), valine-citrulline (val-cit), p-aminobenzyloxycarbonyl (PAB), 6-maleimidocaproyl-valine-citrulline-p-aminobenzyloxycarbonyl (MC-val-cit-PAB) and/or Bis-Maleimido polyethylene glycol (BMPEO).

10. The immunoconjugate of claim 3 , wherein D is auristatin.

11. The immunoconjugate of claim 10 wherein the auristatin is MMAE or MMAF.

12. The immunoconjugate of claim 11 wherein D is monomethyl auristatin E (MMAE), having the structure:

wherein the wavy line indicates the attachment site to the linker L.

13. The immunoconjugate of claim 3 , wherein D is maytansinoid.

14. The immunoconjugate of claim 13 , wherein the maytansinoid is DM1 or DM4, having the structures:

wherein the wavy line indicates the attachment site to the linker L.

15. The immunoconjugate according to claim 1 having a structure:

wherein Val is valine; Cit is citrulline; p is 1, 2, 3, or 4.

16. The immunoconjugate of claim 15 , wherein the heavy chain comprises the amino acid sequence of SEQ ID NO:208 and the light chain comprises the amino acid sequence of SEQ ID NO:207.

17. The immunoconjugate of claim 15 , wherein the antibody is selected from the group consisting of a bispecific antibody, a chimeric antibody, a humanized antibody, and an antibody fragment.

18. The immunoconjugate of claim 3 , wherein the heavy chain comprises the amino acid sequence of SEQ ID NO:232 and the light chain comprises the amino acid sequence of SEQ ID NO:233.

19. The immunoconjugate of claim 1 , wherein the heavy chain comprises the amino acid sequence of SEQ ID NO:208 and the light chain comprises the amino acid sequence of SEQ ID NO:207.

20. The immunoconjugate of claim 1 , wherein the heavy chain comprises the amino acid sequence of SEQ ID NO:232 and the light chain comprises the amino acid sequence of SEQ ID NO:233.

21. The immunoconjugate of claim 3 , wherein the heavy chain comprises the amino acid sequence of SEQ ID NO:208 and the light chain comprises the amino acid sequence of SEQ ID NO:207.

22. The immunoconjugate of claim 15 , wherein the heavy chain comprises the amino acid sequence of SEQ ID NO: 232 and the light chain comprises the amino acid sequence of SEQ ID NO: 233.

23. The immunoconjugate of claim 22 , wherein p is 1 or 2.

24. The immunoconjugate of claim 15 , wherein p is 1 or 2.

25. The immunoconjugate of claim 16 , wherein p is 1 or 2.

26. A pharmaceutical composition comprising an immunoconjugate having the formula:

wherein Val is valine; Cit is citrulline; and p is 1 or 2; and
wherein Ab is an anti-CD79b cysteine engineered antibody comprising a heavy chain, a light chain, and an engineered cysteine at position 118 of the heavy chain according to EU numbering convention, wherein the heavy chain comprises the amino acid sequence of SEQ ID NO: 208 and the light chain comprises the amino acid sequence of SEQ ID NO: 207; and wherein the

is covalently attached to the engineered cysteine.

27. A pharmaceutical composition comprising an immunoconjugate having the formula:

wherein Val is valine; Cit is citrulline; and p is 1 or 2; and
wherein Ab is an anti-CD79b cysteine engineered antibody comprising a heavy chain, a light chain, and an engineered cysteine at position 118 of the heavy chain according to EU numbering convention, wherein the heavy chain comprises the amino acid sequence of SEQ ID NO: 232 and the light chain comprises the amino acid sequence of SEQ ID NO: 233; and wherein the

Assignees

• Genentech Inc

Inventors

• Chen Yvonne
• Dennis Mark
• Dornan David
• Elkins Kristi
• Junutula Jagath Reddy
• Polson Andrew
• Zheng Bing

Classifications

• A61P7/00

  Drugs for disorders of the blood or the extracellular fluid · CPC title

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P5/14

  of the thyroid hormones, e.g. T3, T4 · CPC title

• A61P37/06

  Immunosuppressants, e.g. drugs for graft rejection · CPC title