Methods of treating cancer using anti-pd-l1 antibodies and antiandrogens
US-2019309071-A1 · Oct 10, 2019 · US
US11767362B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-11767362-B1 |
| Application number | US-201716084346-A |
| Country | US |
| Kind code | B1 |
| Filing date | Mar 14, 2017 |
| Priority date | Mar 15, 2016 |
| Publication date | Sep 26, 2023 |
| Grant date | Sep 26, 2023 |
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The invention provides compositions and methods for treating cancers. The methods comprising administering a PD-1 axis binding antagonist and an anti-GPC3 antibody. The compositions comprising a pharmaceutical composition for treating cancer which comprises a PD-1 axis binding antagonist and an anti-GPC3 antibody. Also disclosed are a pharmaceutical composition to be used in combination with a PD-1 axis binding antagonist for treating cancer which comprises an anti-GPC3 antibody as the active ingredient; and a pharmaceutical composition to be used in combination with an anti-GPC3 antibody for treating cancer which comprises as the active ingredient a PD-1 axis binding antagonist.
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The invention claimed is: 1. A method for treating or delaying progression of cancer in an individual, comprising administering a therapeutically effective amount of an anti-GPC3 antibody to the individual, wherein the individual is also being administered atezolizumab, wherein the anti-GPC3 antibody comprises a heavy chain comprising HVR-H1 sequence of SEQ ID NO:42, HVR-H2 sequence of SEQ ID NO: 43, and HVR-H3 sequence of SEQ ID NO: 44; and a light chain comprising HVR-L1 sequence of SEQ ID NO: 45, HVR-L2 sequence of SEQ ID NO: 46, and HVR-L3 sequence of SEQ ID NO: 47, and wherein the cancer is liver cancer. 2. The method according to claim 1 wherein the anti-GPC3 antibody is a humanized antibody. 3. The method according to claim 2 , wherein the anti-GPC3 antibody comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:50 and a light chain variable region comprising the amino acid sequence of SEQ ID NO:52. 4. The method according to claim 1 , wherein the cancer is selected from the group consisting of liver cancer, breast cancer, lung cancer, ovarian cancer, gastric cancer, bladder cancer, pancreatic cancer, endometrial cancer, colon cancer, kidney cancer, esophageal cancer and prostate cancer. 5. A method for treating or delaying progression of cancer in an individual, comprising administering to the individual a therapeutically effective amount of an anti-GPC3 antibody, and administering a therapeutically effective amount of atezolizumab, wherein the anti-GPC3 antibody comprises a heavy chain comprising HVR-H1 sequence of SEQ ID NO:42, HVR-H2 sequence of SEQ ID NO: 43, and HVR-H3 sequence of SEQ ID NO: 44; and a light chain comprising HVR-L1 sequence of SEQ ID NO: 45, HVR-L2 sequence of SEQ ID NO: 46, and HVR-L3 sequence of SEQ ID NO: 47, and wherein the cancer is liver cancer. 6. A method for treating or delaying progression of cancer in an individual, comprising administering a therapeutically effective amount of atezolizumab to the individual, wherein the individual is also being administered a therapeutically effective amount of an anti-GPC3 antibody, wherein the anti-GPC3 antibody comprises a heavy chain comprising HVR-H1 sequence of SEQ ID NO:42, HVR-H2 sequence of SEQ ID NO: 43, and HVR-H3 sequence of SEQ ID NO: 44; and a light chain comprising HVR-L1 sequence of SEQ ID NO: 45, HVR-L2 sequence of SEQ ID NO: 46, and HVR-L3 sequence of SEQ ID NO: 47, and wherein the cancer is liver cancer. 7. The method according to claim 5 wherein the anti-GPC3 antibody is a humanized antibody. 8. The method according to claim 6 wherein the anti-GPC3 antibody is a humanized antibody.
against B7 molecules, e.g. CD80, CD86 · CPC title
Antineoplastic agents · CPC title
Liver or Pancreas · CPC title
containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title
F(ab')2 · CPC title
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