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Last Updated: April 23, 2024

Claims for Patent: 8,778,340


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Summary for Patent: 8,778,340
Title:Anti-angiogenesis therapy for the treatment of ovarian cancer
Abstract: This invention concerns in general treatment of diseases and pathological conditions with anti-VEGF antibodies. More specifically, the invention concerns the treatment of human patients susceptible to or diagnosed with cancer using an anti-VEGF antibody, preferably in combination with one or more additional anti-tumor therapeutic agents for the treatment of ovarian cancer.
Inventor(s): Dupont; Jakob (Hillsborough, CA), Irl; Cornelia (Basel, CH)
Assignee: Genentech, Inc. (So. San Francisco, CA)
Application Number:13/032,532
Patent Claims:1. A method of treating a patient diagnosed with recurrent platinum-sensitive advanced epithelial ovarian, fallopian tube or primary peritoneal cancer, comprising subjecting the patient to a treatment regimen combining carboplatin and gemcitabine with the concurrent administration of 15 mg/kg of an anti-VEGF antibody having a heavy chain variable region comprising the following amino acid sequence: TABLE-US-00017 (SEQ ID NO. 1) EVQLVESGGG LVQPGGSLRL SCAASGYTFT NYGMNWVRQA PGKGLEWVGW INTYTGEPTY AADFKRRFTF SLDTSKSTAY LQMNSLRAED TAVYYCAKYP HYYGSSHWYF DVWGQGTLVT VSS

and a light chain variable region comprising the following amino acid sequence: TABLE-US-00018 (SEQ ID NO. 2) DIQMTQSPSS LSASVGDRVT ITCSASQDIS NYLNWYQQKP GKAPKVLIYF TSSLHSGVPS RFSGSGSGTD FTLTISSLQP EDFATYYCQQ YSTVPWTFGQ GTKVEIKR

followed by anti-VEGF antibody maintenance therapy, and wherein the treatment regimen effectively extends the progression free survival of the patient.

2. The method of claim 1, wherein said anti-VEGF antibody binds the same epitope as the monoclonal anti-VEGF antibody A4.6.1 produced by hybridoma ATCC HB 10709.

3. The method of claim 1, wherein the anti-VEGF antibody is a humanized antibody.

4. The method of claim 3, wherein the anti-VEGF antibody is a humanized A4.6.1 antibody or fragment thereof.

5. The method of claim 3, wherein the anti-VEGF antibody is bevacizumab.

6. The method of claim 1, wherein the carboplatin is administered at an area under the concentration-time curve (AUC) of 4.

7. The method of claim 1, wherein the gemcitabine is administered at 1000 mg/m.sup.2.

8. The method of claim 1, wherein the anti-VEGF antibody maintenance is administered at 15 mg/kg.

9. The method claim 1, wherein the progression free survival of the patient is extended by at least about 2.3 months or more compared to another patient not treated with anti-VEGF antibody.

10. The method of claim 1, wherein the patient is diagnosed with Stage III or Stage IV ovarian cancer.

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