Methods of treating cancers using PD-1 axis binding antagonists and anti-GPC3 antibodies

US11767362B1 · US · B1

Patent metadata
FieldValue
Publication numberUS-11767362-B1
Application numberUS-201716084346-A
CountryUS
Kind codeB1
Filing dateMar 14, 2017
Priority dateMar 15, 2016
Publication dateSep 26, 2023
Grant dateSep 26, 2023

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

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.

First claim

Opening claim text (preview).

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.

Assignees

Inventors

Classifications

  • against B7 molecules, e.g. CD80, CD86 · CPC title

  • Antineoplastic agents · CPC title

  • C07K16/303Primary

    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

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11767362B1 cover?
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 …
Who is the assignee on this patent?
Chugai Pharmaceutical Co Ltd, Genentech Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/2827. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).