Anti-ctla-4 antibodies
US-2017226211-A1 · Aug 10, 2017 · US
US12595307B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12595307-B2 |
| Application number | US-202118001566-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 9, 2021 |
| Priority date | Jun 11, 2020 |
| Publication date | Apr 7, 2026 |
| Grant date | Apr 7, 2026 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Compositions and methods are presented in which selected polypeptide compounds bind to CTLA-4. Most typically, binding is mediated by selected VH and/or VL domains, and preferred compounds are prepared as scFv, IgG, or CAR.
Opening claim text (preview).
What is claimed is: 1 . An antibody or fusion protein comprised thereof, comprising: a variable heavy chain (VH) segment and a variable light chain (VL) segment respectively consisting of SEQ ID NO:60 and SEQ ID NO: 63, SEQ ID NO:61 and SEQ ID NO:63, SEQ ID NO: 62 and SEQ ID NO:63, SEQ ID NO:64 and SEQ ID NO:67, SEQ ID NO:65 and SEQ ID NO:67, SEQ ID NO:66 and SEQ ID NO:67, SEQ ID NO: 68 and SEQ ID NO:69, or SEQ ID NO:70 and SEQ ID NO:71. 2 . The antibody of claim 1 comprising a variable heavy chain (VH) segment and a variable light chain (VL) segment respectively consisting of SEQ ID NO:60 and SEQ ID NO: 63, SEQ ID NO:61 and SEQ ID NO:63, SEQ ID NO:62 and SEQ ID NO:63, SEQ ID NO:64 and SEQ ID NO:67, SEQ ID NO:65 and SEQ ID NO:67, SEQ ID NO:66 and SEQ ID NO:67, SEQ ID NO: 68 and SEQ ID NO:69, or SEQ ID NO:70 and SEQ ID NO:71. 3 . An antibody, comprising a heavy chain comprising a first amino acid sequence of SEQ ID NO. 68 and a light chain comprising a second amino acid sequence of SEQ ID NO. 69, or a heavy chain comprising a first amino acid sequence of SEQ ID NO. 70 and a light chain comprising a second amino acid sequence of SEQ ID NO. 71. 4 . A recombinant nucleic acid, comprising: a first nucleic acid segment encoding a variable heavy chain (VH) peptide sequence and second nucleic acid segment encoding a variable light chain (VL) peptide sequence, wherein the VH and VL peptide sequences combine to form an antibody, scfv, or fusion proteins derived therefrom, and wherein the VH and VL peptides respectively consist of SEQ ID NO:60 and SEQ ID NO:63, SEQ ID NO:61 and SEQ ID NO:63, SEQ ID NO:62 and SEQ ID NO:63, SEQ ID NO: 64 and SEQ ID NO:67, SEQ ID NO: 65 and SEQ ID NO:67, SEQ ID NO: 66 and SEQ ID NO:67, SEQ ID NO: 68 and SEQ ID NO:69, or SEQ ID NO: 70 and SEQ ID NO:71; and wherein the first and second segments are optionally in a bicistronic arrangement. 5 . A recombinant nucleic acid, comprising: a first nucleic acid segment encoding a first amino acid sequence of SEQ ID NO. 68 and second nucleic acid segment encoding a second amino acid sequence of SEQ ID NO. 69, or a first nucleic acid segment encoding a first amino acid sequence of SEQ ID NO. 70 and a second nucleic acid segment encoding a second amino acid sequence of SEQ ID NO. 71. 6 . The recombinant nucleic acid of claim 4 further comprising a third segment encoding a polypeptide that encodes at least a portion of a N-803 or TxM, wherein the N-803 or TxM, when expressed in the cell, has an antigen binding domain that comprises an scfv peptide encoded by the first and second nucleic acid segment. 7 . A method of reducing immune suppression in a patient having a tumor, comprising: administering to the patient a pharmaceutical composition including an antibody or fusion protein of any one of claims 1-3 ; and wherein the pharmaceutical composition is administered to the patient in a dose and a schedule effective to reduce immune suppression in a tumor microenvironment. 8 . A method of using an antibody or fusion protein of any one of claims 1-3 for treating a cancer and/or reducing immune suppression in a patient having a tumor, comprising: administering to the patient the antibody or fusion protein at a dose and schedule effective to treat the tumor and/or reduce immune suppression in a tumor microenvironment.
Single chain antibody (scFv) · CPC title
Valency · CPC title
General or multifunctional contrast agents, e.g. chelated agents · CPC title
Antineoplastic agents · CPC title
for cancer · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.