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公开(公告)号:US12246030B2
公开(公告)日:2025-03-11
申请号:US18167984
申请日:2023-02-13
Applicant: ModernaTX, Inc.
Inventor: Stephen Hoge , Tirtha Chakraborty , Gilles Besin , Ruchi Jain
IPC: C07H21/04 , A61K9/00 , A61K9/127 , A61K31/7115 , C12N15/113 , C12N15/67
Abstract: The disclosure features methods of reducing or inhibiting an anti-drug antibody response in a subject, as well as methods of reducing or inhibiting unwanted immune cell activation in a subject to be treated with a messenger RNA (mRNA), comprising administering to the subject a mRNA, e.g., a chemically modified messenger RNA (mmRNA), encoding a polypeptide of interest, wherein the mRNA comprises at least one microRNA (miR) binding site for a miR expressed in immune cells, such as miR-126 binding site and/or miR-142 binding site, such that an anti-drug antibody response to the polypeptide or interest, or unwanted immune cell activation (e.g., B cell activation, cytokine secretion), is reduced or inhibited in the subject. The disclosure further provides therapeutic treatment regimens designed to reduce or inhibit ADA or unwanted immune cell activation (e.g., B cell activation, cytokine secretion) in a subject being treated with mRNA-based therapeutics.
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公开(公告)号:US20180028664A1
公开(公告)日:2018-02-01
申请号:US15674872
申请日:2017-08-11
Applicant: ModernaTX, Inc.
Inventor: Gilles Besin , Stephen Hoge , Joseph Senn , Kerry Benenato , Staci Sabnis
IPC: A61K47/10 , C12N15/117 , A61K39/39 , C08G65/333 , C08G65/332 , C08G65/335 , A61K31/713 , C08G65/334
CPC classification number: A61K48/0033 , A61K9/127 , A61K31/7115 , A61K31/713 , A61K39/39 , A61K47/10 , A61K47/543 , A61K47/544 , A61K47/60 , A61K47/6929 , A61K48/0066 , A61K2039/55555 , C08G65/3322 , C08G65/3326 , C08G65/33306 , C08G65/3331 , C08G65/33317 , C08G65/33324 , C08G65/3348 , C08G65/3356 , C08G2650/04 , C12N15/117 , C12N15/88 , C12N2310/141 , C12N2310/17 , C12N2320/32
Abstract: This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering agents in vivo including nucleic acids and proteins. These compositions are not subject to accelerated blood clearance and they have an improved toxicity profile in vivo.
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公开(公告)号:US11590157B2
公开(公告)日:2023-02-28
申请号:US17036374
申请日:2020-09-29
Applicant: ModernaTX, Inc.
Inventor: Stephen Hoge , Tirtha Chakraborty , Gilles Besin , Ruchi Jain
IPC: C07H21/02 , A61K31/7115 , C12N15/67 , A61K9/00 , A61K9/127 , C12N15/113
Abstract: The disclosure features methods of reducing or inhibiting an anti-drug antibody response in a subject, as well as methods of reducing or inhibiting unwanted immune cell activation in a subject to be treated with a messenger RNA (mRNA), comprising administering to the subject a mRNA, e.g., a chemically modified messenger RNA (mmRNA), encoding a polypeptide of interest, wherein the mRNA comprises at least one microRNA (miR) binding site for a miR expressed in immune cells, such as miR-126 binding site and/or miR-142 binding site, such that an anti-drug antibody response to the polypeptide or interest, or unwanted immune cell activation (e.g., B cell activation, cytokine secretion), is reduced or inhibited in the subject. The disclosure further provides therapeutic treatment regimens designed to reduce or inhibit ADA or unwanted immune cell activation (e.g., B cell activation, cytokine secretion) in a subject being treated with mRNA-based therapeutics.
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公开(公告)号:US20180147298A1
公开(公告)日:2018-05-31
申请号:US15674107
申请日:2017-08-10
Applicant: ModernaTX, Inc.
Inventor: Gilles Besin , Stephen Hoge , Joseph Senn , Kerry Benenato , Staci Sabnis
Abstract: This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering agents in vivo including nucleic acids and proteins. These compositions are not subject to accelerated blood clearance and they have an improved toxicity profile in vivo.
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公开(公告)号:US20190117798A1
公开(公告)日:2019-04-25
申请号:US16229509
申请日:2018-12-21
Applicant: ModernaTX, Inc.
Inventor: Gilles Besin , Stephen Hoge , Joseph Senn , Kerry Benenato , Staci Sabnis
IPC: A61K48/00 , C12N15/88 , A61K47/10 , A61K47/54 , A61K31/7115 , A61K9/127 , A61K47/69 , A61K47/60 , A61K39/39 , C08G65/332 , C08G65/333 , C08G65/334 , C08G65/335 , C12N15/117 , A61K31/713
Abstract: This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering agents in vivo including nucleic acids and proteins. These compositions are not subject to accelerated blood clearance and they have an improved toxicity profile in vivo.
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公开(公告)号:US10207010B2
公开(公告)日:2019-02-19
申请号:US15674872
申请日:2017-08-11
Applicant: ModernaTX, Inc.
Inventor: Gilles Besin , Stephen Hoge , Joseph Senn , Kerry Benenato , Staci Sabnis
IPC: C12N15/88 , A61K9/127 , A61K48/00 , A61K47/54 , A61K47/69 , A61K47/60 , A61K31/713 , A61K39/39 , A61K47/10 , C08G65/332 , C08G65/333 , C08G65/334 , C08G65/335 , C12N15/117 , A61K31/7115 , A61K39/00
Abstract: This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering agents in vivo including nucleic acids and proteins. These compositions are not subject to accelerated blood clearance and they have an improved toxicity profile in vivo.
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公开(公告)号:US11905525B2
公开(公告)日:2024-02-20
申请号:US16603111
申请日:2018-04-05
Applicant: ModernaTX, Inc.
Inventor: Luis Brito , Gilles Besin
CPC classification number: C12N15/88 , A61K9/0019 , A61K9/1271 , A61K31/7105 , A61K47/12 , A61K47/28 , C12N2310/141
Abstract: This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering nucleic acids in vivo. These compositions have reduced immune activation resulting in accelerated blood clearance and/or anti-drug antibodies and they have an improved toxicity profile and therapeutic index in vivo.
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公开(公告)号:US20220265857A1
公开(公告)日:2022-08-25
申请号:US17583674
申请日:2022-01-25
Applicant: ModernaTX,Inc.
Inventor: Gilles Besin , Stephen Hoge , Joseph Senn , Kerry Benenato , Staci Sabnis
IPC: A61K48/00 , A61K9/127 , C12N15/88 , A61K31/7115 , A61K47/14 , A61K47/18 , A61K47/54 , A61K47/69 , A61K47/60 , A61K31/713 , A61K39/39 , A61K47/10 , C08G65/332 , C08G65/333 , C08G65/334 , C08G65/335 , C12N15/117
Abstract: This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering agents in vivo including nucleic acids and proteins. These compositions are not subject to accelerated blood clearance and they have an improved toxicity profile in vivo.
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公开(公告)号:US11285222B2
公开(公告)日:2022-03-29
申请号:US16599661
申请日:2019-10-11
Applicant: ModernaTX, Inc.
Inventor: Gilles Besin , Stephen Hoge , Joseph Senn , Kerry Benenato , Staci Sabnis
IPC: A61K48/00 , A61K9/127 , C12N15/88 , A61K31/7115 , A61K47/14 , A61K47/18 , A61K47/54 , A61K47/69 , A61K47/60 , A61K31/713 , A61K39/39 , A61K47/10 , C08G65/332 , C08G65/333 , C08G65/334 , C08G65/335 , C12N15/117 , A61K39/00
Abstract: This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering agents in vivo including nucleic acids and proteins. These compositions are not subject to accelerated blood clearance and they have an improved toxicity profile in vivo.
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公开(公告)号:US10849920B2
公开(公告)日:2020-12-01
申请号:US15761220
申请日:2016-10-05
Applicant: ModernaTX, Inc.
Inventor: Stephen Hoge , Tirtha Chakraborty , Gilles Besin , Ruchi Jain
IPC: A61K48/00 , C07H21/04 , A61K31/7115 , C12N15/67 , A61K9/00 , A61K9/127 , C12N15/113
Abstract: The disclosure features methods of reducing or inhibiting an anti-drug antibody response in a subject, as well as methods of reducing or inhibiting unwanted immune cell activation in a subject to be treated with a messenger RNA (mRNA), comprising administering to the subject a mRNA, e.g., a chemically modified messenger RNA (mmRNA), encoding a polypeptide of interest, wherein the mRNA comprises at least one microRNA (miR) binding site for a miR expressed in immune cells, such as miR-126 binding site and/or miR-142 binding site, such that an anti-drug antibody response to the polypeptide or interest, or unwanted immune cell activation (e.g., B cell activation, cytokine secretion), is reduced or inhibited in the subject. The disclosure further provides therapeutic treatment regimens designed to reduce or inhibit AD A or unwanted immune cell activation (e.g., B cell activation, cytokine secretion) in a subject being treated with mRNA-based therapeutics.
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