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公开(公告)号:US20230270836A1
公开(公告)日:2023-08-31
申请号:US17938823
申请日:2022-10-07
Applicant: ModernaTX, Inc.
Inventor: Giuseppe Ciaramella , Sunny Himansu , Vladimir Presnyak , Kerry Benenato , Ellalahewage Sathyajith Kumarasinghe
IPC: A61K39/12 , A61P31/14 , A61K31/7115 , C12N15/86
CPC classification number: A61K39/12 , A61P31/14 , A61K31/7115 , C12N15/86 , A61K2039/53
Abstract: The disclosure relates to Lassa virus, Nipah virus, and betacoronavirus ribonucleic acid vaccines as well as methods of using the vaccines and compositions comprising the vaccines.
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公开(公告)号:US20230270685A1
公开(公告)日:2023-08-31
申请号:US17989941
申请日:2022-11-18
Applicant: ModernaTX, Inc.
Inventor: Paolo Martini , Vladimir Presnyak , Kerry Benenato , Stephen Hoge , Iain McFadyen , Ellalahewage Sathyajith Kumarasinghe
CPC classification number: A61K9/5123 , A61K9/1272 , A61K38/52 , A61K48/005 , A61P3/00 , A61P43/00 , C12N9/90 , C12N15/52 , C12Y504/99002 , A61K38/00
Abstract: The disclosure relates to polynucleotides comprising an open reading frame of linked nucleosides encoding human methylmalonyl-CoA mutase precursor, human methylmalonyl-CoA mutase (MCM) mature form, or functional fragments thereof. In some embodiments, the disclosure includes methods of treating methylmalonic acidemia in a subject in need thereof comprising administering an mRNA encoding an MCM polypeptide.
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33.
公开(公告)号:US20230233475A1
公开(公告)日:2023-07-27
申请号:US17928684
申请日:2021-06-01
Applicant: ModernaTX, Inc.
Inventor: Kerry Benenato , Kristine Burke , Jingsong Cao , Paloma Hoban Giangrande , Edward J. Hennessy , Stephen Hoge , Jaclyn Milton , Staci Sabnis , Timothy Salerno , Matthew Theisen
IPC: A61K9/51 , A61K31/7088 , A61K9/00 , C12N9/16 , A61P35/00
CPC classification number: A61K9/5123 , A61K31/7088 , A61K9/0019 , C12Y301/03009 , C12N9/16 , A61P35/00
Abstract: This disclosure relates to ionizable lipid-based lipid nanoparticles for delivery of mRNA encoding glucose-6-phosphatase. Lipid nanoparticle/mRNA therapies of the invention increase and/or restore deficient levels of glucose-6-phosphatase expression and activity in subjects and are useful for the treatment of glycogen storage disease type 1a (GSD-Ia). Lipid nanoparticle/mRNA therapies of the invention increase glucose production and reduce the abnormal accumulation of glycogen and glucose-6-phosphate associated with GSD-Ia.
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公开(公告)号:US11660341B2
公开(公告)日:2023-05-30
申请号:US17202829
申请日:2021-03-16
Applicant: ModernaTX, Inc.
Inventor: Joshua P. Frederick , Susannah Hewitt , Ailin Bai , Stephen G. Hoge , Vladimir Presnyak , Iain McFadyen , Kerry Benenato , Ellalahewage Sathyajith Kumarasinghe
IPC: A61K48/00 , A61K39/395 , C07K14/54 , C07K14/705 , C07K16/28 , A61K39/39 , A61K45/06 , A61K31/713 , A61K39/00 , A61P35/00
CPC classification number: A61K39/39558 , A61K31/713 , A61K39/0011 , A61K39/39 , A61K45/06 , A61K48/005 , C07K14/54 , C07K14/5434 , C07K14/5443 , C07K14/705 , C07K14/70503 , C07K14/70532 , C07K14/70575 , C07K14/70596 , C07K16/2818 , A61K2039/505 , A61K2039/51 , A61K2039/53 , A61K2039/585 , A61P35/00 , C07K2317/76 , C07K2319/30 , C07K2319/32 , A61K31/713 , A61K2300/00
Abstract: The present disclosure relates to the use of nucleic acid (e.g., mRNA) combination therapies for the treatment of cancer. The disclosure provides compositions, and methods for their preparation, manufacture, and therapeutic use, wherein those compositions comprise at least two polynucleotides (e.g., mRNAs) in combination wherein the at least two polynucleotides are selected from the group consisting of (i) a polynucleotide encoding an immune response primer (e.g., IL23), (ii) a polynucleotide encoding an immune response co-stimulatory signal (e.g., OX40L), (iii) a polynucleotide encoding a checkpoint inhibitor (e.g., an anti CTLA-4 antibody), and, (iv) a combination thereof. The therapeutic methods disclosed herein comprise, e.g., the administration of a combination therapy disclosed herein for the treatment of cancer, e.g., by reducing the size of a tumor or inhibiting the growth of a tumor, in a subject in need thereof. In some aspects, the combination therapies disclosed herein disclosed are administered intratumorally.
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公开(公告)号:US11649461B2
公开(公告)日:2023-05-16
申请号:US16570351
申请日:2019-09-13
Applicant: ModernaTX, Inc.
Inventor: Paolo Martini , Stephen G. Hoge , Kerry Benenato , Vladimir Presnyak , Iain Mcfadyen , Ellalahewage Sathyajith Kumarasinghe , Xuling Zhu , Lin Tung Guey , Staci Sabnis
CPC classification number: C12N15/67 , A61K9/5123 , A61K38/47 , A61P3/00 , C12N9/2465 , C12Y302/01022 , A61K48/00
Abstract: The invention relates to mRNA therapy for the treatment of Fabry disease. mRNAs for use in the invention, when administered in vivo, encode human the α-galactosidase A (GLA), isoforms thereof, functional fragments thereof, and fusion proteins comprising GLA. mRNAs of the invention are preferably encapsulated in lipid nanoparticles (LNPs) to effect efficient delivery to cells and/or tissues in subjects, when administered thereto. mRNA therapies of the invention increase and/or restore deficient levels of GLA expression and/or activity in subjects. mRNA therapies of the invention further decrease levels of toxic metabolites associated with deficient GLA activity in subjects, namely Gb3 and lyso-Gb3.
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公开(公告)号:US11497807B2
公开(公告)日:2022-11-15
申请号:US17155592
申请日:2021-01-22
Applicant: ModernaTX, Inc.
Inventor: Giuseppe Ciaramella , Sunny Himansu , Vladimir Presnyak , Kerry Benenato , Ellalahewage Sathyajith Kumarasinghe
IPC: A61K39/12 , A61P31/14 , A61K31/7115 , C12N15/86 , A61K39/00
Abstract: Provide herein are Lassa virus, Nipah virus, and betacoronavirus ribonucleic acid vaccines as well as methods of using the vaccines and compositions comprising the vaccines.
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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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38.
公开(公告)号:US11001861B2
公开(公告)日:2021-05-11
申请号:US16302341
申请日:2017-05-18
Applicant: ModernaTX, Inc.
Inventor: Paolo Martini , Stephen Hoge , Kerry Benenato , Vladimir Presnyak , Iain McFadyen , Ellalahewage Sathyajith Kumarasinghe , Ding An , Staci Sabnis
Abstract: The invention relates to mRNA therapy for the treatment of galactosemia type 1 (Gal-1). mRNAs for use in the invention, when administered in vivo, encode human galactose-1-phosphate uridylyltransferase (GALT), isoforms thereof, functional fragments thereof, and fusion proteins comprising GALT. mRNAs of the invention are preferably encapsulated in lipid nanoparticles (LNPs) to effect efficient delivery to cells and/or tissues in subjects, when administered thereto. mRNA therapies of the invention increase and/or restore deficient levels of GALT expression and/or activity in subjects. mRNA therapies of the invention further decrease levels of toxic metabolites associated with deficient GALT activity in subjects, namely galactose-1-phosphate (Gal-1-P).
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公开(公告)号:US10730924B2
公开(公告)日:2020-08-04
申请号:US16025302
申请日:2018-07-02
Applicant: ModernaTX, Inc.
Inventor: Barry Ticho , Nadege Briancon-Eris , Zhinan Xia , Athanasios Dousis , Seymour de Picciotto , Vladimir Presnyak , Stephen Hoge , Iain Mcfadyen , Kerry Benenato , Ellalahewage Sathyajith Kumarasinghe
IPC: C12N15/62 , A61K47/14 , C07K14/64 , A61K31/7105 , A61K47/69 , A61P9/00 , A61K38/17 , C07K16/26 , C12N15/52 , A61K9/127 , A61K38/00 , A61K9/00
Abstract: The invention relates to mRNA therapy for the treatment of fibrosis and/or cardiovascular disease. mRNAs for use in the invention, when administered in vivo, encode human relaxin, isoforms thereof, functional fragments thereof, and fusion proteins comprising relaxin. mRNAs of the invention are preferably encapsulated in lipid nanoparticles (LNPs) to effect efficient delivery to cells and/or tissues in subjects, when administered thereto. mRNA therapies of the invention increase and/or restore deficient levels of relaxin expression and/or activity in subjects. mRNA therapies of the invention further decrease levels of toxic metabolites associated with deficient relaxin activity in subjects.
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公开(公告)号:US10556018B2
公开(公告)日:2020-02-11
申请号:US15674107
申请日:2017-08-10
Applicant: ModernaTX, Inc.
Inventor: Gilles Besin , Stephen Hoge , Joseph Senn , Kerry Benenato , Staci Sabnis
IPC: A61K48/00 , A61K9/127 , C12N15/88 , A61K47/54 , A61K47/69 , A61K47/60 , A61K31/713 , A61K39/39 , A61K47/10 , C08G65/332 , C08G65/333 , C08G65/334 , C08G65/335 , C12N15/117 , A61K31/7115 , A61K47/14 , A61K47/18 , 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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