You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: April 24, 2024

Claims for Patent: 9,416,362


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 9,416,362
Title:Methods and compositions for reducing viral genome amounts in a target cell
Abstract: Methods and compositions for reducing viral genome amounts in a target cell are provided. In the subject methods, the activity of a miRNA is inhibited in a manner sufficient to reduce the amount of viral genome in the target cell, e.g., by introducing a miRNA inhibitory agent in the target cell. Also provided are pharmaceutical compositions, kits and systems for use in practicing the subject methods. The subject invention finds use in a variety of applications, including the treatment of subjects suffering from a viral mediated disease condition, e.g., an HCV mediated disease condition.
Inventor(s): Sarnow; Peter (Palo Alto, CA), Jopling; Catherine L. (Beeston, GB), Lancaster; Alissa M. (Portland, OR)
Assignee: The Board of Trustees of The Leland Stanford Junior University (Palo Alto, CA)
Application Number:14/280,156
Patent Claims:1. A pharmaceutical composition comprising: a) an antisense oligonucleotide complementary to miR-122 such that said antisense oligonucleotide binds to miR-122 and inhibits its activity, wherein the antisense oligonucleotide comprises a nucleotide sequence of SEQ ID NO:15; and b) a pharmaceutically acceptable carrier; wherein said composition is prepared by a method of i) providing said antisense oligonucleotide as a powder, and ii) reconstituting said powder into a liquid form with said pharmaceutically acceptable carrier.

2. The pharmaceutical composition of claim 1, wherein said pharmaceutically acceptable carrier is sterile water.

3. The pharmaceutical composition of claim 1, wherein the antisense oligonucleotide complementary to miR-122 comprises a 2'-O-methyl modification.

4. The pharmaceutical composition of claim 1, wherein said composition comprises 0.1 to 90% by weight said antisense oligonucleotide.

5. The pharmaceutical composition of claim 1, wherein said composition comprises 1 to 30% by weight said antisense oligonucleotide.

6. The pharmaceutical composition of claim 1, wherein said composition is formulated for parenteral administration.

7. The pharmaceutical composition of claim 6, wherein said parenteral administration comprises intravenous administration.

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.