JPWO2020089819A5 - - Google Patents

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JPWO2020089819A5
JPWO2020089819A5 JP2021518633A JP2021518633A JPWO2020089819A5 JP WO2020089819 A5 JPWO2020089819 A5 JP WO2020089819A5 JP 2021518633 A JP2021518633 A JP 2021518633A JP 2021518633 A JP2021518633 A JP 2021518633A JP WO2020089819 A5 JPWO2020089819 A5 JP WO2020089819A5
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substance
alpha
kit
agent
medicament according
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JP2021518633A
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JP2022505022A (en
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Priority claimed from PCT/IB2019/059331 external-priority patent/WO2020089819A1/en
Publication of JP2022505022A publication Critical patent/JP2022505022A/en
Publication of JPWO2020089819A5 publication Critical patent/JPWO2020089819A5/ja
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Claims (21)

対象の身体に少なくとも部分的に導入され、その上にアルファ放出原子が取り付けられている少なくとも1つの線源と;
細胞内病原体に対する細胞質センサーを活性化する少なくとも1つの物質と;そして
前記少なくとも1つの線源と前記少なくとも1つの物質を含む無菌パッケージと;
を有することを特徴とする、患者の治療のためのキット。
at least one radiation source at least partially introduced into a subject's body and having alpha-emitting atoms attached thereon;
at least one substance that activates a cytoplasmic sensor for intracellular pathogens; and a sterile package containing said at least one radiation source and said at least one substance;
A kit for treating a patient, comprising:
アルファ放出原子またはそれらの娘放射性核種の線源からの制御可能な放出を可能にする態様で、アルファ放出原子が線源に取り付けられている、ことを特徴とする請求項に記載のキット。 2. The kit of claim 1 , wherein the alpha-emitting atoms are attached to the source in a manner that allows controllable release from the source of alpha-emitting atoms or their daughter radionuclides. 前記アルファ放出原子はラジウム原子を含む、ことを特徴とする請求項に記載のキット。 2. The kit of claim 1 , wherein said alpha emitting atoms comprise radium atoms. 前記少なくとも1つの物質がDNAメチルトランスフェラーゼ(DNMT)阻害剤を含む、ことを特徴とする請求項のいずれかに記載のキット。 Kit according to any one of claims 1 to 3 , characterized in that said at least one substance comprises a DNA methyltransferase (DNMT) inhibitor. 前記DNAメチルトランスフェラーゼ(DNMT)阻害剤がデシタビンを含む、ことを特徴とする請求項に記載のキット。 5. The kit of claim 4 , wherein said DNA methyltransferase (DNMT) inhibitor comprises decitabine. 前記少なくとも1つの物質が、病原体模倣物の細胞質送達に適した送達剤を伴う病原体模倣物をさらに含む、ことを特徴とする請求項に記載のキット。 5. The kit of claim 4 , wherein said at least one substance further comprises a pathogen mimetic with a delivery agent suitable for cytoplasmic delivery of the pathogen mimetic. 前記少なくとも1つの物質が、病原体模倣物の細胞質送達に適した送達剤を伴う病原体模倣物を含む、請求項のいずれかに記載のキット。 4. The kit of any of claims 1-3 , wherein said at least one substance comprises a pathogen mimetic with a delivery agent suitable for cytoplasmic delivery of the pathogen mimetic. アルファ放射体放射線療法によって誘発される加速された組織修復に対抗する支持的治療薬をさらに前記無菌パッケージに含む、ことを特徴とする請求項のいずれかに記載のキット。 The kit of any of claims 1-3 , further comprising in the sterile package a supportive therapeutic agent against accelerated tissue repair induced by alpha-emitter radiotherapy. 前記支持的治療薬が、炎症をダウンレギュレートする薬剤を含む、ことを特徴とする請求項に記載のキット。 9. The kit of claim 8 , wherein said supportive therapeutic agent comprises an agent that downregulates inflammation. 患者の腫瘍の処置のための医薬品として使用される、細胞内病原体に対する細胞質センサーを活性化する物質であって、前記医薬品の投与パターンは、1回以上のセッションで治療的に有効な量の前記物質を前記腫瘍に投与するステップと;そして前記物質の投与から2週間以内に腫瘍内アルファ放射体放射線療法で前記腫瘍を処置するステップと;を有する、A substance that activates a cytosolic sensor against intracellular pathogens for use as a pharmaceutical agent for the treatment of a tumor in a patient, wherein the dosage pattern of said pharmaceutical agent is a therapeutically effective amount of said agent in one or more sessions. administering an agent to said tumor; and treating said tumor with intratumoral alpha-emitter radiotherapy within two weeks of administration of said agent;
ことを特徴とする、医薬品として使用される物質。A substance used as a drug, characterized by:
前記物質は、病原体模倣物の細胞質送達に適した送達剤を備える前記病原体模倣物を有する、ことを特徴とする請求項10に記載の、医薬品として使用される物質。11. A substance for use as a pharmaceutical product according to claim 10, characterized in that said substance comprises said pathogen mimetic with a delivery agent suitable for cytoplasmic delivery of said pathogen mimetic. 前記物質はウイルス模倣物を有する、ことを特徴とする請求項10または11に記載の、医薬品として使用される物質。12. Substance for use as a medicament according to claim 10 or 11, characterized in that said substance has a viral mimetic. 前記物質はポリエチレンイミン(PEI)を備えるpolyICを有する、ことを特徴とする請求項10-12のいずれかに記載の、医薬品として使用される物質。A substance for use as a medicament according to any of claims 10-12, characterized in that said substance has a polyIC with polyethylenimine (PEI). 前記物質はpolyICLCを有する、ことを特徴とする請求項10-12のいずれかに記載の、医薬品として使用される物質。A substance for use as a medicament according to any of claims 10-12, characterized in that said substance has polyICLC. 前記物質は腫瘍溶解性ウイルスを有する、ことを特徴とする請求項10に記載の、医薬品として使用される物質。11. Substance for use as a medicament according to claim 10, characterized in that said substance carries an oncolytic virus. 前記物質はDNAメチルトランスフェラーゼ(DNMT)阻害剤を有する、ことを特徴とする請求項10に記載の、医薬品として使用される物質。11. Substance for use as a medicament according to claim 10, characterized in that said substance has a DNA methyltransferase (DNMT) inhibitor. 前記物質はデシタビンを有する、ことを特徴とする請求項16に記載の医薬品として使用される物質。17. Substance for use as a medicament according to claim 16, characterized in that said substance comprises decitabine. 前記医薬品の投与パターンはさらに、チェックポイント阻害のための支持的治療薬を投与するステップを有する、ことを特徴とする請求項10-17のいずれかに記載の、医薬品として使用される物質。A substance for use as a medicament according to any of claims 10-17, characterized in that said pharmaceutical dosing pattern further comprises administering a supportive therapeutic agent for checkpoint inhibition. 前記支持的治療薬はチェックポイント遮断薬を有する、ことを特徴とする請求項18に記載の、医薬品として使用される物質。19. Substance for use as a pharmaceutical product according to claim 18, characterized in that said supportive therapeutic agents comprise checkpoint blockers. 前記腫瘍内アルファ放射体放射線療法はラジウム原子を担持する線源により提供される、ことを特徴とする請求項10-19のいずれかに記載の、医薬品として使用される物質。A substance for use as a medicament according to any of claims 10-19, characterized in that said intratumoral alpha-emitter radiotherapy is provided by a source carrying radium atoms. 前記腫瘍内アルファ放射体放射線療法は、アルファ放出原子またはそれらの娘放射性核種の線源からの制御可能な放出を可能にする態様で搭載される、アルファ放出原子を担持する線源により提供される、ことを特徴とする請求項10-20のいずれかに記載の、医薬品として使用される物質。Said intratumoral alpha-emitter radiotherapy is provided by a source carrying alpha-emitting atoms mounted in a manner that allows controllable release from the source of alpha-emitting atoms or their daughter radionuclides. A substance for use as a medicament according to any one of claims 10 to 20, characterized in that .
JP2021518633A 2018-11-01 2019-10-31 Activation of cytoplasmic plasma sensor for intracellular alpha radiator radiation and intracellular pathogens Pending JP2022505022A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862753930P 2018-11-01 2018-11-01
US62/753,930 2018-11-01
PCT/IB2019/059331 WO2020089819A1 (en) 2018-11-01 2019-10-31 Intratumoral alpha-emitter radiation and activation of cytoplasmatic sensors for intracellular pathogen

Publications (2)

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JP2022505022A JP2022505022A (en) 2022-01-14
JPWO2020089819A5 true JPWO2020089819A5 (en) 2022-10-19

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US (1) US20210379096A1 (en)
EP (1) EP3873598A4 (en)
JP (1) JP2022505022A (en)
KR (1) KR20210087949A (en)
CN (2) CN112912137B (en)
AU (2) AU2019370892B2 (en)
CA (1) CA3114299A1 (en)
SG (1) SG11202102627PA (en)
WO (1) WO2020089819A1 (en)

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