Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Application
Filed:
July 22, 2022
Publication date:
December 1, 2022
Applicants:
Regulus Therapeutics Inc., The Board of Regents of The University of Texas System
Inventors:
Charles R. ALLERSON, Vishal D. PATEL, B. Nelson CHAU, John R. ANDROSAVICH
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Application
Filed:
March 21, 2022
Publication date:
July 7, 2022
Applicants:
Regulus Therapeutics Inc., The Board of Regents of The University of Texas System
Inventors:
Charles R. ALLERSON, Vishal D. PATEL, B. Nelson CHAU, John R. ANDROSAVICH
Abstract: Provided herein are methods for oral administration of oligonucleotides. Further provided herein are methods for oral administration of modified oligonucleotides targeted to microRNA.
Abstract: Described herein are compositions and methods for the inhibition of miR-10b activity. The compositions may be administered to subjects with cancer, such as glioma.
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Application
Filed:
October 5, 2021
Publication date:
January 27, 2022
Applicants:
Regulus Therapeutics Inc., Board of Regents of The University of Texas System
Inventors:
John R. ANDROSAVICH, B. Nelson CHAU, Vishal D. PATEL
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Grant
Filed:
March 19, 2020
Date of Patent:
November 9, 2021
Assignees:
Regulus Therapeutics Inc., Board of Regents of The University of Texas System
Inventors:
John R. Androsavich, B. Nelson Chau, Vishal D. Patel
Abstract: Described herein are compositions and methods for the inhibition of miR-122 activity. The compositions have certain nucleoside modifications that yield potent inhibitors of miR-122 activity and comprise moieties that facilitate delivery to the liver. The compositions may be administered to subjects infected with hepatitis C virus, as a treatment for hepatitis C virus and related conditions.
Type:
Application
Filed:
May 7, 2019
Publication date:
June 10, 2021
Applicant:
Regulus Therapeutics Inc.
Inventors:
Charles R. Allerson, Steven S. Neben, Timothy Wright
Abstract: Described herein are compositions and methods for the inhibition of miR-122 activity. The compositions have certain nucleoside modifications that yield potent inhibitors of miR-122 activity. The compounds may comprise conjugates to facilitate delivery to the liver. The compositions may be administered to subjects infected with hepatitis C virus, as a treatment for hepatitis C virus and related conditions.
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Abstract: Described herein are conjugated modified oligonucleotides that are complementary to a target RNA. The conjugate facilitates cellular uptake of the modified oligonucleotide, resulting improved potency.
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Application
Filed:
August 27, 2020
Publication date:
December 17, 2020
Applicants:
Regulus Therapeutics Inc., The Board of Regents of the University of Texas System
Inventors:
Charles R. ALLERSON, Vishal D. PATEL, B. Nelson CHAU, John R. ANDROSAVICH
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Application
Filed:
August 27, 2020
Publication date:
December 17, 2020
Applicants:
Regulus Therapeutics Inc., The Board of Regents of the University of Texas System
Inventors:
Charles R. ALLERSON, Vishal D. PATEL, B. Nelson CHAU, John R. ANDROSAVICH
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Application
Filed:
March 19, 2020
Publication date:
July 23, 2020
Applicants:
Regulus Therapeutics Inc., Board of Regents of the University of Texas System
Inventors:
John R. ANDROSAVICH, B. Nelson CHAU, Vishal D. PATEL
Abstract: Provided herein are methods for the treatment of polycystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Abstract: Provided herein are methods for the treatment of poly-cystic kidney disease, including autosomal dominant polycystic kidney disease, using modified oligonucleotides targeted to miR-17.
Type:
Grant
Filed:
August 25, 2016
Date of Patent:
April 28, 2020
Assignees:
Regulus Therapeutics Inc., Board of Regents of the University of Texas System
Inventors:
John R. Androsavich, B. Nelson Chau, Vishal D. Patel
Abstract: Compounds, compositions and methods are provided for modulating the expression and function of small non-coding RNAs. The compositions comprise oligomeric compounds, targeted to small non-coding RNAs. Methods of using these compounds for modulation of small non-coding RNAs as well as downstream targets of these RNAs and for diagnosis and treatment of disease associated with small non-coding RNAs are also provided.
Type:
Grant
Filed:
September 6, 2018
Date of Patent:
March 10, 2020
Assignee:
Regulus Therapeutics Inc.
Inventors:
C. Frank Bennett, Susan M. Freier, Richard H. Griffey
Abstract: Described herein are conjugated modified oligonucleotides that are complementary to a target RNA. The conjugate facilitates cellular uptake of the modified oligonucleotide, resulting improved potency.
Abstract: Provided herein are methods for the treatment of liver cancer. These methods encompass the administration of a compound comprising a modified oligonucleotide, wherein the modified oligonucleotide is targeted to a miRNA. Also provided herein are compositions for the treatment of liver cancer. Such compositions include compounds comprising a modified oligonucleotide, wherein the modified oligonucleotide is targeted to a miRNA. Certain miRNAs have been identified as overexpressed in liver cancer, such as, for example, hepatocellular carcinoma, and are thus selected for targeting by modified oligonucleotides. Further, certain miRNAs have been identified as overexpressed in hepatocellular carcinoma cells exposed to dioxin, and are thus selected for targeting by modified oligonucleotides. Antisense inhibition of certain of these miRNAs has been found to inhibit cell proliferation and induce apoptosis.
Abstract: Described herein are compounds comprising modified oligonucleotides that are complementary to miR-103 and/or miR-107 and methods of treating diseases and disorders using the compounds.
Type:
Application
Filed:
September 25, 2018
Publication date:
May 23, 2019
Applicant:
Regulus Therapeutics Inc.
Inventors:
Balkrishen Bhat, Neil W. Gibson, Diedre MacKenna, Brandee Wagner, David P. Bartel