DK3140320T3 - Peptidvaccine, der omfatter mutant ras-peptid og kemoterapeutisk middel - Google Patents
Peptidvaccine, der omfatter mutant ras-peptid og kemoterapeutisk middel Download PDFInfo
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- DK3140320T3 DK3140320T3 DK15720986.7T DK15720986T DK3140320T3 DK 3140320 T3 DK3140320 T3 DK 3140320T3 DK 15720986 T DK15720986 T DK 15720986T DK 3140320 T3 DK3140320 T3 DK 3140320T3
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- A61K2039/515—Animal cells
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
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- A61K2039/55511—Organic adjuvants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/58—Medicinal preparations containing antigens or antibodies raising an immune response against a target which is not the antigen used for immunisation
- A61K2039/585—Medicinal preparations containing antigens or antibodies raising an immune response against a target which is not the antigen used for immunisation wherein the target is cancer
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Claims (20)
- PEPTID VACCINE, DER OMFATTER MUTANT RAS-PEPTID OG KEMOTERAPEUTISK MIDDEL1. Mindst ét peptid, der er egnet til frembringelse af et immunrespons, hvor peptidet eller hvert peptid svarer til et fragment af et vildtype-RAS-protein men har én aminosyresubstitution deraf, til anvendelse i cancerbehandling ved samtidig eller sekventiel administration med en pyrimidinanalog eller et farmaceutisk acceptabelt salt deraf, hvor peptidet eller hvert peptid omfatter et område af mindst 8 aminosyrer, der indbefatter position 12 eller 13 af RAS-proteinet, og hvor aminosyresubstitutionen af peptidet eller hvert peptid er ved henholdsvis position 12 eller 13 og er valgt fra en G13A-, G13C-, G13D-, G13R-, G13S-, G13V-, G12A-, G12C-, G12D-, G12R-, G12S eller en G12V-substitution.
- 2. Mindst ét peptid til anvendelse ifølge krav 1, hvor det mindst ene peptid omfatter to eller flere peptider, hvor hvert peptid har en forskellig aminosyresubstitution.
- 3. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor det mindst ene peptid omfatter: et peptid med en G13D-substitution et peptid med en G12A-substitution et peptid med en G12C-substitution et peptid med en G12D-substitution et peptid med en G12R-substitution et peptid med en G12S-substitution og et peptid med en G12V-substitution.
- 4. Mindst ét peptid til anvendelse ifølge krav 3, hvor det mindst ene peptid omfatter et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 13, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 14, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 15, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 16, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 17, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 18 og et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 19.
- 5. Mindst ét peptid til anvendelse ifølge krav 1 eller 2, hvor det mindst ene peptid omfatter: et peptid med en G13D-substitution et peptid med en G13C-substitution et peptid med en G12A-substitution et peptid med en G12C-substitution et peptid med en G12D-substitution et peptid med en G12R-substitution et peptid med en G12S-substitution og et peptid med en G12V-substitution.
- 6. Mindst ét peptid til anvendelse ifølge krav 5, hvor det mindst ene peptid omfatter et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 13, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 14, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 15, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 16, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 17, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 18, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 19 og et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 20.
- 7. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor pyrimidinanalogen er gemcitabin eller et farmaceutisk acceptabelt salt deraf.
- 8. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor det mindst ene peptid omfatter et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 13, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 14, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 15, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 16, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 17, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 18, et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 19 og et peptid, der består af sekvensen repræsenteret ved SEQ ID NO: 20, og hvor pyrimidinanalogen er gemcitabin.
- 9. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor canceren omfatter celler, der udtrykket et muteret RAS-protein.
- 10. Mindst ét peptid til anvendelse ifølge krav 9, hvor canceren er pankreascancer.
- 11. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor pyrimidinanalogen eller det farmaceutisk acceptable salt deraf først administreres mindst tre uger efter den første dosis af det mindst ene peptid.
- 12. Mindst ét peptid til anvendelse ifølge krav 9, hvor canceren er resekteret pankreascancer og pyrimidinanalogen eller det farmaceutisk acceptable salt deraf først administreres 12 uger eller færre efter kirurgisk resektion af pankreascanceren.
- 13. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor pyrimidinanalogen eller det farmaceutisk acceptable salt deraf administreres inden for 24 timer efter det mindst ene peptid.
- 14. Mindst ét peptid til anvendelse ifølge krav 13, hvor pyrimidinanalogen administreres, efter at det mindst ene peptid er administreret.
- 15. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor det mindst ene peptid administreres i en dosering å 0,01-10 mg.
- 16. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor pyrimidinanalogen eller det farmaceutisk acceptable salt deraf administreres ved en dosis å 100-10.000 mg/m2.
- 17. Mindst ét peptid til anvendelse ifølge et hvilket som helst foregående krav, hvor det mindst ene peptid og pyrimidinanalogen administreres samtidigt eller sekventielt af mindst to gange, hvor der er mindst én uge mellem hver administreringsgang.
- 18. Mindst én T-celle, der er specifik for det mindst ene peptid ifølge af et hvilket som helst af de foregående krav, eller et T-cellepræparat, der omfatter T-celler, der er specifikke for det mindst ene peptid som defineret i et hvilket som helst af de foregående krav, når det præsenteres på et MHC-molekyle, til anvendelse i cancerbehandling ved samtidig eller sekventiel administration med en pyrimidinanalog eller et farmaceutisk acceptabelt salt deraf.
- 19. Farmaceutisk sammensætning, der omfatter mindst ét peptid som defineret i et hvilket som helst af kravene 1-17, eller mindst én T-celle eller et T-cellepræparat som defineret i krav 18, til anvendelse i cancerbehandling ved kombineret eller sekventiel administration med en pyrimidinanalog eller et farmaceutisk acceptabelt salt deraf.
- 20. Pyrimidinanalog eller et farmaceutisk acceptabelt salt deraf, til anvendelse i cancerbehandling ved samtidig eller sekventiel administration med mindst ét peptid, der er egnet til frembringelse af et immunrespons, hvor peptidet eller hvert peptid svarer til et fragment af et vildtype-RAS-protein men har én aminosyresubstitution deraf, hvor peptidet eller hvert peptid omfatter et område af mindst 8 aminosyrer, der indbefatter position 12 eller 13 af RAS-proteinet, og hvor aminosyresubstitutionen af peptidet eller hvert peptid er ved henholdsvis position 12 eller 13, og er valgt fra en G13A-, G13C-, G13D-, G13R-, G13S-, G13V-, G12A-, G12C-, G12D-, G12R-, G12S- eller en G12V-substitution.
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EP14167265 | 2014-05-06 | ||
PCT/EP2015/059861 WO2015169804A1 (en) | 2014-05-06 | 2015-05-05 | Peptide vaccine comprising mutant ras peptide and chemotherapeutic agent |
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US (1) | US9757439B2 (da) |
EP (1) | EP3140320B1 (da) |
JP (2) | JP2017514847A (da) |
KR (1) | KR20170002563A (da) |
CN (1) | CN106414493A (da) |
AU (1) | AU2015257774B2 (da) |
BR (1) | BR112016025764A2 (da) |
CA (1) | CA2947963A1 (da) |
CL (1) | CL2016002794A1 (da) |
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ES (1) | ES2716923T3 (da) |
IL (1) | IL248671B (da) |
MX (1) | MX2016014414A (da) |
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CA2933126A1 (en) | 2013-12-09 | 2015-06-18 | Targovax Asa | A peptide mixture |
AU2017347837A1 (en) | 2016-10-26 | 2019-06-06 | Modernatx, Inc. | Messenger ribonucleic acids for enhancing immune responses and methods of use thereof |
US20190351039A1 (en) | 2017-02-01 | 2019-11-21 | Modernatx, Inc. | Immunomodulatory therapeutic mrna compositions encoding activating oncogene mutation peptides |
US11771749B2 (en) | 2017-02-03 | 2023-10-03 | The Medical College Of Wisconsin, Inc. | KRAS peptide vaccine compositions and method of use |
WO2020002650A1 (en) | 2018-06-29 | 2020-01-02 | Targovax Asa | A formulation |
CN114573688A (zh) * | 2018-10-19 | 2022-06-03 | 杭州纽安津生物科技有限公司 | 通用性多肽疫苗及其在制备治疗/预防胰腺癌药物中的应用 |
CA3141084A1 (en) * | 2019-06-12 | 2020-12-17 | Vikram JUNEJA | Neoantigen compositions and uses thereof |
CN113416241B (zh) * | 2020-04-09 | 2022-04-08 | 北京臻知医学科技有限责任公司 | 一种用于诱导肿瘤特异性免疫响应的通用型抗原肽库及试剂盒 |
WO2022026620A1 (en) * | 2020-07-29 | 2022-02-03 | Sqz Biotechnologies Company | Methods to stimulate immune responses to mutant ras using nucleated cells |
EP4188425A1 (en) * | 2020-07-29 | 2023-06-07 | SQZ Biotechnologies Company | Methods to stimulate immune responses to mutant ras using anucleate cells |
CA3202725A1 (en) * | 2020-11-24 | 2022-06-02 | Shanghai GenBase Biotechnology Co., Ltd. | Ras mutant epitope peptide and t cell receptor recognizing ras mutant |
WO2023220434A2 (en) * | 2022-05-12 | 2023-11-16 | The Johns Hopkins University | Neoantigen vaccines for cancer prevention |
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GB9103974D0 (en) | 1991-02-26 | 1991-04-10 | Norsk Hydro As | Therapeutically useful peptides or peptide fragments |
GB2328689A (en) | 1997-08-27 | 1999-03-03 | Norsk Hydro As | Peptides based on the p21 ras proto-oncogene protein for the treatment of cancer |
NO309798B1 (no) * | 1999-04-30 | 2001-04-02 | Targovax As | Peptidblanding, samt farmasoytisk sammensetning og kreftvaksine som innbefatter peptidblandingen |
WO2004058157A2 (en) | 2002-12-16 | 2004-07-15 | Globeimmune, Inc. | Yeast-based vaccines as immunotherapy |
US20140199405A1 (en) * | 2013-01-11 | 2014-07-17 | Abraxis Bioscience, Llc | Method for treating cancer based on mutation status of k-ras |
CA2933126A1 (en) | 2013-12-09 | 2015-06-18 | Targovax Asa | A peptide mixture |
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IL248671B (en) | 2021-08-31 |
CN106414493A (zh) | 2017-02-15 |
EP3140320A1 (en) | 2017-03-15 |
EP3140320B1 (en) | 2018-12-26 |
SG10201809701TA (en) | 2018-12-28 |
MX2016014414A (es) | 2017-02-23 |
SG11201608712PA (en) | 2016-11-29 |
US20170065694A1 (en) | 2017-03-09 |
CA2947963A1 (en) | 2015-11-12 |
AU2015257774A1 (en) | 2016-12-22 |
JP2020100650A (ja) | 2020-07-02 |
JP2017514847A (ja) | 2017-06-08 |
KR20170002563A (ko) | 2017-01-06 |
CL2016002794A1 (es) | 2017-06-09 |
IL248671A0 (en) | 2017-01-31 |
WO2015169804A1 (en) | 2015-11-12 |
US9757439B2 (en) | 2017-09-12 |
JP7304629B2 (ja) | 2023-07-07 |
AU2015257774B2 (en) | 2018-12-20 |
RU2700929C2 (ru) | 2019-09-24 |
ES2716923T3 (es) | 2019-06-18 |
RU2016147527A (ru) | 2018-06-08 |
BR112016025764A2 (pt) | 2018-01-16 |
RU2016147527A3 (da) | 2019-01-21 |
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