AU2020264484A1 - Compositions and methods for the treatment of cancer using a CDB engineered T cell therapy - Google Patents
Compositions and methods for the treatment of cancer using a CDB engineered T cell therapy Download PDFInfo
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- AU2020264484A1 AU2020264484A1 AU2020264484A AU2020264484A AU2020264484A1 AU 2020264484 A1 AU2020264484 A1 AU 2020264484A1 AU 2020264484 A AU2020264484 A AU 2020264484A AU 2020264484 A AU2020264484 A AU 2020264484A AU 2020264484 A1 AU2020264484 A1 AU 2020264484A1
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- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
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- C12N5/0634—Cells from the blood or the immune system
- C12N5/0636—T lymphocytes
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- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/70503—Immunoglobulin superfamily
- C07K14/7051—T-cell receptor (TcR)-CD3 complex
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- A61K40/00—Cellular immunotherapy
- A61K40/10—Cellular immunotherapy characterised by the cell type used
- A61K40/11—T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells
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- A61K40/32—T-cell receptors [TCR]
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- A61K40/00—Cellular immunotherapy
- A61K40/40—Cellular immunotherapy characterised by antigens that are targeted or presented by cells of the immune system
- A61K40/41—Vertebrate antigens
- A61K40/42—Cancer antigens
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K40/40—Cellular immunotherapy characterised by antigens that are targeted or presented by cells of the immune system
- A61K40/41—Vertebrate antigens
- A61K40/42—Cancer antigens
- A61K40/4201—Neoantigens
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- C07K14/61—Growth hormone [GH], i.e. somatotropin
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- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
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- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
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- C12N15/1137—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
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- C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
- C12N15/90—Stable introduction of foreign DNA into chromosome
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0071—Oxidoreductases (1.) acting on paired donors with incorporation of molecular oxygen (1.14)
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
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- C07K2319/00—Fusion polypeptide
- C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
- C07K2319/02—Fusion polypeptide containing a localisation/targetting motif containing a signal sequence
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- C07K2319/50—Fusion polypeptide containing protease site
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- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/10—Type of nucleic acid
- C12N2310/20—Type of nucleic acid involving clustered regularly interspaced short palindromic repeats [CRISPR]
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- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
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- C12N2510/00—Genetically modified cells
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962841748P | 2019-05-01 | 2019-05-01 | |
| US201962841753P | 2019-05-01 | 2019-05-01 | |
| US62/841,753 | 2019-05-01 | ||
| US62/841,748 | 2019-05-01 | ||
| PCT/US2020/030818 WO2020223537A1 (en) | 2019-05-01 | 2020-04-30 | Compositions and methods for the treatment of cancer using a cdb engineered t cell therapy |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2020264484A1 true AU2020264484A1 (en) | 2021-11-04 |
Family
ID=73029470
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2020264484A Pending AU2020264484A1 (en) | 2019-05-01 | 2020-04-30 | Compositions and methods for the treatment of cancer using a CDB engineered T cell therapy |
| AU2020266579A Abandoned AU2020266579A1 (en) | 2019-05-01 | 2020-04-30 | Compositions and methods for the treatment of cancer using a TET2 engineered T cell therapy |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2020266579A Abandoned AU2020266579A1 (en) | 2019-05-01 | 2020-04-30 | Compositions and methods for the treatment of cancer using a TET2 engineered T cell therapy |
Country Status (11)
| Country | Link |
|---|---|
| US (4) | US20210085720A1 (https=) |
| EP (2) | EP3962938A4 (https=) |
| JP (2) | JP7717619B2 (https=) |
| KR (2) | KR20220004703A (https=) |
| CN (1) | CN113748127B (https=) |
| AU (2) | AU2020264484A1 (https=) |
| CA (2) | CA3151385A1 (https=) |
| IL (2) | IL287643A (https=) |
| MX (2) | MX2021013225A (https=) |
| SG (2) | SG11202111865UA (https=) |
| WO (3) | WO2020223478A1 (https=) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3114788A1 (en) * | 2018-09-28 | 2020-04-02 | Memorial Sloan-Kettering Cancer Center | Immunoresponsive cells expressing dominant negative fas and uses thereof |
| US12344656B2 (en) * | 2019-09-06 | 2025-07-01 | Crispr Therapeutics Ag | Genetically engineered T cells having improved persistence in culture |
| WO2021216993A1 (en) * | 2020-04-24 | 2021-10-28 | Pact Pharma, Inc. | Methods of determining gene editing efficiencies in cells |
| WO2022109277A1 (en) * | 2020-11-20 | 2022-05-27 | Pact Pharma, Inc. | COMPOSITIONS AND METHODS FOR THE TREATMENT OF CANCER USING A TGFβRII ENGINEERED T CELL THERAPY |
| CA3201767A1 (en) * | 2020-12-14 | 2022-06-23 | Thomas M. Schmitt | Compositions and methods for cellular immunotherapy |
| WO2022140361A1 (en) * | 2020-12-22 | 2022-06-30 | Ludwig Institute For Cancer Research Ltd | Genetically engineered lymphocytes for adoptive cell therapy |
| US20240108652A1 (en) * | 2021-02-18 | 2024-04-04 | University Of Florida Research Foundation, Incorporated | Enhancing metabolic fitness of t cells to treat cancer |
| AU2022227686A1 (en) | 2021-02-25 | 2023-07-27 | Lyell Immunopharma, Inc. | Ror1 targeting chimeric antigen receptor |
| EP4298230A1 (en) | 2021-02-25 | 2024-01-03 | Lyell Immunopharma, Inc. | Codon-optimized nucleotide sequences encoding an ap-1 transcription factor |
| WO2022242644A1 (zh) * | 2021-05-18 | 2022-11-24 | 赛斯尔擎生物技术(上海)有限公司 | 修饰细胞的方法 |
| KR20240021216A (ko) * | 2021-06-11 | 2024-02-16 | 팩트 파마, 인크. | 세포 생성물을 감정하는 방법 |
| EP4405464A4 (en) * | 2021-09-21 | 2025-12-03 | Univ Chicago | METHODS AND COMPOSITION USING PATIENT-DERIVED AUTOLOGOUS NEOANTIGENS FOR CANCER TREATMENT |
| JP2024540099A (ja) | 2021-10-28 | 2024-10-31 | ライエル・イミュノファーマ・インコーポレイテッド | Ror1結合タンパク質を発現する細胞を培養する方法 |
| KR20240112376A (ko) | 2021-10-28 | 2024-07-18 | 라이엘 이뮤노파마, 인크. | c-Jun을 발현하는 세포를 배양하는 방법 |
| CN114373511B (zh) * | 2022-03-15 | 2022-08-30 | 南方医科大学南方医院 | 基于5hmC分子标志物检测的肠癌模型及肠癌模型构建方法 |
| WO2023212507A1 (en) * | 2022-04-26 | 2023-11-02 | Fred Hutchinson Cancer Center | Compositions and methods for cellular immunotherapy |
| WO2024026490A1 (en) | 2022-07-28 | 2024-02-01 | Sqz Biotechnologies Company | Polynucleotides encoding linked antigens and uses thereof |
| JP2025529540A (ja) * | 2022-09-19 | 2025-09-04 | エメンドバイオ・インコーポレイテッド | Tet2の両アレルノックアウト |
| CN120202302A (zh) * | 2022-09-19 | 2025-06-24 | 埃门多生物公司 | Ctla4双等位基因敲除 |
| AU2023347845A1 (en) * | 2022-09-19 | 2025-04-10 | Emendobio Inc. | Biallelic knockout of faslg |
| WO2024064952A1 (en) | 2022-09-23 | 2024-03-28 | Lyell Immunopharma, Inc. | Methods for culturing nr4a-deficient cells overexpressing c-jun |
| WO2024064958A1 (en) | 2022-09-23 | 2024-03-28 | Lyell Immunopharma, Inc. | Methods for culturing nr4a-deficient cells |
| WO2024077174A1 (en) | 2022-10-05 | 2024-04-11 | Lyell Immunopharma, Inc. | Methods for culturing nr4a-deficient cells |
| CN116179495B (zh) * | 2022-11-28 | 2025-06-06 | 上海恩凯细胞技术有限公司 | 转基因免疫细胞及其应用 |
| WO2025010272A1 (en) | 2023-07-03 | 2025-01-09 | Neoimmunetech, Inc. | Heterodimeric fc molecules and uses thereof |
| WO2025027088A1 (en) * | 2023-07-31 | 2025-02-06 | T-Knife Gmbh | An enhanced chimeric human cd8 co-receptor, a nucleic acid encoding the enhanced chimeric human cd8 co-receptor, corresponding vectors, isolated t-cells transduced with the nucleic acid or corresponding vectors and kits for preparing them, as well as corresponding pharmaceutical compositions and methods for treating a patient having a disease |
| AU2024332117A1 (en) * | 2023-08-25 | 2026-02-12 | T-Knife Gmbh | Chimeric human cd 95 switch receptor, t-cell expressing said receptor together with an engineered t-cell receptor, respective vectors, kits, pharmaceutical compositions and methods for treating a patient having a disease |
| WO2025217398A1 (en) | 2024-04-10 | 2025-10-16 | Lyell Immunopharma, Inc. | Methods for culturing cells with improved culture medium |
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