IP Library Granted Patent US 8,075,892
Granted Patent B2
US 8,075,892 · App. 11/780,640 · Granted Dec 13, 2011

Treatment with anti-ErbB2 antibodies

Assignee: Genentech, Inc.
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Quick Facts
Patent No.
US 8,075,892
App. No.
11/780,640
Granted
Dec 13, 2011
Kind
B2
Abstract

The present invention concerns the treatment of disorders characterized by the overexpression of ErbB2. More specifically, the invention concerns the treatment of human patients susceptible to or diagnosed with cancer overexpressing ErbB2 with a combination of an anti-ErbB2 antibody and a chemotherapeutic agent other than an anthracycline, e.g. doxorubicin or epirubicin. The invention further provides a method of treating cancer in a human patient comprising administering effective amounts of an anti-ErbB2 antibody and a cardioprotectant to the patient.

Claims (6)

1. A method for the treatment of a human patient with breast cancer characterized by overexpression of ErbB2 receptor, comprising administering a combination of an anti-ErbB2 antibody and capecitabine to the human patient in an amount effective to treat the cancer, under direction of an attending physician, wherein the attending physician is provided with instructions including a warning that the treatment is not to be performed in combination with an anthracycline derivative and wherein said antibody binds to epitope 4D5 within the ErbB2 extracellular domain sequence.

2. The method of claim 1 wherein said breast cancer is metastatic breast carcinoma.

3. The method of claim 1 wherein said antibody is a humanized 4D5 anti-ErbB2 antibody.

4. The method of claim 1 wherein efficacy is defined in terms of time to disease progression or response rate.

5. The method of claim 1 wherein the antibody is not conjugated with the capecitabine.

6. A method for the treatment of a human patient with an ErbB2-overexpressing breast cancer, comprising administering a combination of a humanized 4D5 anti-ErbB2 antibody and capecitabine, to the human patient in an amount effective to treat the cancer, under direction of an attending physician, wherein the treatment increases time to disease progression compared to therapy with capecitabine alone, and wherein the attending physician is provided with instructions including a warning that the treatment is not to be performed in combination with an anthracycline derivative.

Continuity (4)
Division 10909998 · Aug 2, 2004
Continuation 09209023 · Dec 10, 1998
Provisional Application 60069346 · Dec 12, 1997
Related Publication 20070292419A1 · Dec 20, 2007