Methods and compositions relating to anti-PD1 antibody reagents

US11427636B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11427636-B2
Application numberUS-201816608275-A
CountryUS
Kind codeB2
Filing dateMay 1, 2018
Priority dateMay 1, 2017
Publication dateAug 30, 2022
Grant dateAug 30, 2022

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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.

Described herein are novel anti-PD1 antibody reagents (e.g., antibodies, antigen-binding fragments thereof, and/or chimeric antigen receptors). Also described herein antibody-drug conjugates or kits comprising the disclosed antibody reagents, as well as methods of treating cancer by administering the disclosed antibody reagents.

First claim

Opening claim text (preview).

What is claimed herein is: 1. An antibody, antibody reagent, antigen-binding fragment thereof, or chimaeric antigen receptor (CAR), that specifically binds an PD1 polypeptide, said antibody reagent, antigen-binding portion thereof, or CAR comprising: heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 23-25 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 26-28; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 29-31 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 32-34; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 35-37 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 38-40; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 41-43 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 44-46; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 47-49 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 50-52; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 53-55 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 56-58; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 59-61 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 62-64; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 65-67 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 68-70; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 71-73 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 74-76; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 77-79 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 80-82; or heavy chain CDRs having the amino acid sequences of SEQ ID NOs: 83-85 and light chain CDRs having the amino acid sequences of SEQ ID NOs: 86-88. 2. The antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 1 , comprising the heavy chain sequence of any of SEQ ID NOs: 1, 3, 5, 7, 9, 11, 13, 15, 17, 19 or 21. 3. The antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 1 , comprising the light chain sequence of any of SEQ ID NOs: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, or 22. 4. The antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 1 , comprising: the heavy chain sequence of SEQ ID NO: 1 and the light chain sequence of SEQ ID NO: 2; or the heavy chain sequence of SEQ ID NO: 3 and the light chain sequence of SEQ ID NO: 4; or the heavy chain sequence of SEQ ID NO: 5 and the light chain sequence of SEQ ID NO: 6; or the heavy chain sequence of SEQ ID NO: 7 and the light chain sequence of SEQ ID NO: 8; or the heavy chain sequence of SEQ ID NO: 9 and the light chain sequence of SEQ ID NO: 10; or the heavy chain sequence of SEQ ID NO: 11 and the light chain sequence of SEQ ID NO: 12; or the heavy chain sequence of SEQ ID NO: 13 and the light chain sequence of SEQ ID NO: 14; or the heavy chain sequence of SEQ ID NO: 15 and the light chain sequence of SEQ ID NO: 16; or the heavy chain sequence of SEQ ID NO: 17 and the light chain sequence of SEQ ID NO: 18; or the heavy chain sequence of SEQ ID NO: 19 and the light chain sequence of SEQ ID NO: 20; or the heavy chain sequence of SEQ ID NO: 21 and the light chain sequence of SEQ ID NO: 22. 5. The antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 4 , further comprising a conservative substitution in a sequence not comprised by a CDR. 6. The antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 1 , wherein the antibody reagent or antigen-binding fragment thereof is fully human or fully humanized. 7. The antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 1 , wherein the antibody reagent or antigen-binding fragment thereof is fully humanized except for the CDR sequences. 8. The antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 1 , wherein the reagent or fragment is selected from the group consisting of: an immunoglobulin molecule, a monoclonal antibody, a chimeric antibody, a CDR-grafted antibody, a humanized antibody, a Fab, a Fab′, a F(ab′)2, a Fv, a disulfide linked Fv, a scFv, a single domain antibody, a diabody, a multispecific antibody, a dual specific antibody, an anti-idiotypic antibody, and a bispecific antibody. 9. A composition comprising the antibody, antibody reagent, antigen-binding portion thereof, or CAR of claim 1 , and a chemotherapeutic agent. 10. The composition of claim 9 , wherein the antibody, antibody reagent, antigen-binding portion thereof, or CAR is conjugated to the chemotherapeutic agent. 11. A method of treating cancer in a subject in need thereof, the method comprising administering the antibody, antibody reagent, antigen-binding fragment thereof, or CAR of claim 1 to the subject. 12. The method of claim 11 , wherein the cancer is selected from the group consisting of: Non-small cell lung cancer; melanoma; metastatic melanoma; renal cell carcinoma; squamous cell carcinoma of the head and neck; Hodgkin lymphoma; classical Hodgkin lymphoma; and urothelial carcinoma.

Assignees

Inventors

Classifications

  • involving compounds localised on the membrane of tumour or cancer cells · CPC title

  • of the skin, e.g. melanoma · CPC title

  • of the blood, e.g. leukaemia · CPC title

  • of the liver or pancreas · CPC title

  • Antineoplastic agents · CPC title

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What does patent US11427636B2 cover?
Described herein are novel anti-PD1 antibody reagents (e.g., antibodies, antigen-binding fragments thereof, and/or chimeric antigen receptors). Also described herein antibody-drug conjugates or kits comprising the disclosed antibody reagents, as well as methods of treating cancer by administering the disclosed antibody reagents.
Who is the assignee on this patent?
Childrens Medical Ct Corp
What technology area does this patent fall under?
Primary CPC classification G01N33/57525. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Aug 30 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).