IP Library Granted Patent US 9,360,484
Granted Patent B2
US 9,360,484 · App. 14/078,241 · Granted Jun 7, 2016

Anti-FcRH5 antibodies and immunoconjugates and methods of use

Inventors: Kristi Elkins (San Francisco, CA); Andrew Polson (San Francisco, CA); Allen Ebens (San Carlos, CA); Camelia Adams (San Jose, CA); Bing Zheng (Mountain View, CA); Jagath R. Junutula (Fremont, CA); Jo-Anne Hongo (Redwood City, CA); Yan Wu (Foster City, CA)
Assignee: GENENTECH, INC.
G01N33/6854A61K31/138A61K31/4196A61K31/454A61K31/4745A61K31/517A61K31/56A61K31/568A61K31/5685A61K31/69A61K33/24A61K38/19A61K39/0011A61K39/39533A61K39/39558A61K47/48384A61K47/48561C07K16/283C07K16/2803G01N33/574G01N33/6857A61K2039/505C07K2317/24C07K2317/522C07K2317/73
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Quick Facts
Patent No.
US 9,360,484
App. No.
14/078,241
Granted
Jun 7, 2016
Kind
B2
Abstract

The present invention is directed to compositions of matter useful for the treatment of hematopoietic tumor in mammals and to methods of using those compositions of matter for the same.

Claims (28)

1. A method of determining the presence of FcRH5 in a biological sample suspected of containing FcRH5, said method comprising exposing said sample to an isolated monoclonal anti-FcRH5 antibody comprising:

(a) a light chain variable domain comprising:

(i) HVR-L1 comprising the amino acid sequence of SEQ ID NO: 26;

(ii) HVR-L2 comprising the amino acid sequence of SEQ ID NO: 27; and

(iii) HVR-L3 comprising the amino acid sequence of SEQ ID NO: 28; and

(b) a heavy chain variable domain comprising:

(i) HVR-H1 comprising the amino acid sequence of SEQ ID NO: 35;

(ii) HVR-H2 comprising the amino acid sequence of SEQ ID NO: 36; and

(iii) HVR-H3 comprising the amino acid sequence of SEQ ID NO: 37, and determining binding of said antibody to FcRH5 in said sample wherein binding of said antibody to FcRH5 in said sample is indicative of the presence of said protein in said sample.

2. The method of claim 1 wherein the biological sample is from a patient suspected of having a B cell proliferative disorder.

3. The method of claim 2 wherein the B cell proliferative disorder is selected from lymphoma, non-Hodgkins lymphoma (NHL), aggressive NHL, relapsed aggressive NHL, relapsed indolent NHL, refractory NHL, refractory indolent NHL, chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma, leukemia, hairy cell leukemia (HCL), acute lymphocytic leukemia (ALL), multiple myeloma, and mantle cell lymphoma.

4. The method of claim 3 , wherein the B cell proliferative disorder is multiple myeloma.

5. The method of claim 3 , wherein the B cell proliferative disorder is chronic lymphocytic leukemia.

6. The method of claim 1 , wherein the antibody is covalently attached to a label selected from a fluorescent dye, a radioisotope, biotin, or a metal-complexing ligand.

7. The method of claim 6 , wherein the antibody is covalently attached to a fluorescent dye.

8. The method of claim 6 , wherein the antibody is covalently attached to a radioisotope.

9. The method of claim 6 , wherein the antibody is covalently attached to biotin.

10. The method of claim 6 , wherein the antibody is covalently attached to a metal-complexing ligand.

11. The method of claim 1 , wherein the isolated monoclonal anti-FcRH5 antibody comprises a heavy chain variable domain comprising amino acid sequence of SEQ ID NO:40 and a light chain variable domain comprising amino acid sequence of SEQ ID NO:30.

12. The method of claim 11 , wherein the biological sample is from a patient suspected of having a B cell proliferative disorder.

13. The method of claim 12 , wherein the B cell proliferative disorder is selected from lymphoma, non-Hodgkins lymphoma (NHL), aggressive NHL, relapsed aggressive NHL, relapsed indolent NHL, refractory NHL, refractory indolent NHL, chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma, leukemia, hairy cell leukemia (HCL), acute lymphocytic leukemia (ALL), multiple myeloma, and mantle cell lymphoma.

14. The method of claim 13 , wherein the B cell proliferative disorder is multiple myeloma.

15. The method of claim 13 , wherein the B cell proliferative disorder is chronic lymphocytic leukemia.

16. The method of claim 11 , wherein the antibody is covalently attached to a label selected from a fluorescent dye, a radioisotope, biotin, or a metal-complexing ligand.

17. The method of claim 16 , wherein the antibody is covalently attached to a fluorescent dye.

18. The method of claim 16 , wherein the antibody is covalently attached to a radioisotope.

19. The method of claim 16 , wherein the antibody is covalently attached to biotin.

20. The method of claim 16 , wherein the antibody is covalently attached to a metal-complexing ligand.

Continuity (6)
Continuation 13682581 · Nov 20, 2012
Division 12751819 · Mar 31, 2010
Provisional Application 61211695 · Apr 1, 2009
Provisional Application 61166217 · Apr 2, 2009
Provisional Application 61266972 · Dec 4, 2009
Related Publication 20140106374A1 · Apr 17, 2014