Combination therapy of cancer with anti-endoglin antibodies and anti-vegf agents

US2018371072A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2018371072-A1
Application numberUS-201816112304-A
CountryUS
Kind codeA1
Filing dateAug 24, 2018
Priority dateAug 17, 2009
Publication dateDec 27, 2018
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present application relates to compositions of chimeric anti-endoglin antibodies and anti-VEGF agents. Another aspect relates to the use of chimeric anti-endoglin antibodies and Bevacizumab. Another aspect relates to the use of the compositions to inhibit VEGF induced sprouting. Another aspect relates to the use of the compositions to inhibit angiogenesis.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of inhibiting VEGF induced sprouting by contacting cells with a composition comprising a chimeric anti-endoglin antibody and a composition comprising a VEGF antagonist; said chimeric anti-endoglin antibody comprising a light chain variable region (V L ) having an amino acid sequence set forth as SEQ ID NO: 1; a light chain constant region (C L ) having an amino acid sequence set forth as SEQ ID NO: 2; a heavy chain variable region (V H ) having an amino acid sequence set forth as SEQ ID NO: 3; and a constant region (Fc) having an amino acid sequence set forth as SEQ ID NO: 4. 2 . A method of inhibiting cancer growth in a subject comprising administering a composition comprising a chimeric anti-endoglin antibody and a composition comprising a VEGF antagonist; said chimeric anti-endoglin antibody comprising a light chain variable region (V L ) having an amino acid sequence set forth as SEQ ID NO: 1; a light chain constant region (C L ) having an amino acid sequence set forth as SEQ ID NO: 2; a heavy chain variable region (V H ) having an amino acid sequence set forth as SEQ ID NO: 3; and a constant region (Fc) having an amino acid sequence set forth as SEQ ID NO: 4. 3 . A method of treating an angiogenesis-related disease in a subject comprising administering a composition comprising a chimeric anti-endoglin antibody and a composition comprising a VEGF antagonist; said chimeric anti-endoglin antibody comprising a light chain variable region (V L ) having an amino acid sequence set forth as SEQ ID NO: 1; a light chain constant region (C L ) having an amino acid sequence set forth as SEQ ID NO: 2; a heavy chain variable region (V H ) having an amino acid sequence set forth as SEQ ID NO: 3; and a constant region (Fc) having an amino acid sequence set forth as SEQ ID NO: 4. 4 . The method of any of the preceding claims, wherein said compositions further comprise an acceptable carrier or excipient. 5 . The method of any of the preceding claims, wherein said anti-endoglin antibody is further labeled with a therapeutic label, a diagnostic label, or both. 6 . The method of any of the preceding claims, wherein said VEGF antagonist is further labeled with a therapeutic label, a diagnostic label, or both. 7 . The method of any one of claims 3 - 6 , wherein the angiogenesis-related disease is a cancer, or a metastasis. 8 . The method of any one of claims 2 - 7 , wherein the cancer is a solid tumor. 9 . The method of claim 7 , wherein the cancer is an epithelial based tumor 10 . The method of claim 7 , wherein the cancer is selected from a lung cancer, a gynecologic malignancy, a melanoma, a breast cancer, a pancreatic cancer, an ovarian cancer, a uterine cancer, a colorectal cancer, a prostate cancer, a kidney cancer, a head cancer, a pancreatic cancer, a liver cancer (hepatocellular cancer), a uterine cancer, a neck cancer, a kidney cancer (renal cell cancer), a sarcoma, a myeloma, and a lymphoma. 11 . The method of any one of claims 3 - 6 , wherein the angiogenesis-related disease is an ocular disease characterized by angiogenesis/neovascularization, diabetic nephropathy, inflammatory bowel disease (IBD), rheumatoid arthritis, osteoarthritis, a cancer, or a metastasis. 12 . The method of claim 11 , wherein the ocular disease is macular degeneration. 13 . The method of claim 11 , wherein the ocular disease is diabetic retinopathy. 14 . The method of claim 11 , wherein the angiogenesis-related disease is inflammatory bowel disease (IBD). 15 . The method of claim 11 , wherein the angiogenesis-related disease is rheumatoid arthritis. 16 . The method of claim 11 , wherein the angiogenesis-related disease is osteoarthritis. 17 . The method of any of the preceding claims wherein chimeric anti-endoglin antibody is present in the composition an amount of about 0.01 mg/kg, about 0.05 mg/kg, about 0.1 mg/kg, about 0.5 mg/kg, about 1 mg/kg, about 5 mg/kg, about 10 mg/kg, about 20 mg/kg, about 30 mg/kg. 18 . The method of any of the preceding claims wherein the VEGF antagonist is present in the composition an amount of about 2.5 mg/kg, about 5 mg/kg, about 7.5 mg/kg, about 10 mg/kg or about 15 mg/kg. 19 . The method of any one of the preceding claims wherein the chimeric anti-endoglin antibody and the VEGF antagonist are present in the same composition. 20 . The method of any one of the preceding claims wherein the chimeric anti-endoglin antibody and the VEGF antagonist are present in different compositions. 21 . The method of any one of the preceding claims wherein the chimeric anti-endoglin antibody and the VEGF antagonist are administered sequentially. 22 . The method of any one of the preceding claims wherein the chimeric anti-endoglin antibody and the VEGF antagonist are administered concurrently. 23 . The method of any one of the preceding claims wherein the chimeric anti-endoglin antibody and the VEGF antagonist are administered at the same site. 24 . The method of any one of the preceding claims wherein the chimeric anti-endoglin antibody and the VEGF antagonist are administered at different sites. 25 . The method of any one of the preceding claims wherein the VEGF antagonist is an anti-VEGF antibody. 26 . The method of claim 25 wherein the anti-VEGF antibody is bevacizumab. 27 . The method of any one of claims 2 - 26 , further comprising administering one or more angiogenesis inhibitors. 28 . The method of claim 27 , wherein the angiogenesis inhibitor is chemotherapy, a VEGF receptor inhibitor or a combination thereof.

Assignees

Inventors

Classifications

  • Antineoplastic agents · CPC title

  • specific for metastasis · CPC title

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

  • for hyperglycaemia, e.g. antidiabetics · CPC title

  • Drugs for disorders of the cardiovascular system · CPC title

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Frequently asked questions

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What does patent US2018371072A1 cover?
The present application relates to compositions of chimeric anti-endoglin antibodies and anti-VEGF agents. Another aspect relates to the use of chimeric anti-endoglin antibodies and Bevacizumab. Another aspect relates to the use of the compositions to inhibit VEGF induced sprouting. Another aspect relates to the use of the compositions to inhibit angiogenesis.
Who is the assignee on this patent?
Tracon Pharmaceuticals Inc, Health Research Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/22. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Dec 27 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).