IP Library Granted Patent US 11,040,057
Granted Patent B2
US 11,040,057 · App. 16/313,754 · Granted Jun 22, 2021

Pharmaceutical compositions and methods for potentiating gene silencing

Inventors: Dong Ki Lee (Gyeonggi-do, KR); Da Seul Son (Gyeonggi-do, KR); Yang Hee Kim (Gyeonggi-do, KR)
Assignee: OliX Pharmaceuticals, Inc.
A61K31/713A61K31/137A61K31/277A61K31/444A61K31/4422A61K31/4439A61K31/497A61K31/554A61K31/665C12N15/113C12N2310/11C12N2310/14C12N2310/315C12N2310/321C12N2310/346C12N2310/3515C12N2320/31
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Quick Facts
Patent No.
US 11,040,057
App. No.
16/313,754
Granted
Jun 22, 2021
Kind
B2
Abstract

In various aspects and embodiments, the invention provides compounds or agents that potentiate siRNA cellular entry or activity, and provides methods for identifying such compounds or agents. Exemplary agents that act as L-type calcium channel blockers are described herein, and are shown to potentiate gene silencing with cp-asiRNAs.

Claims (18)

1. A method of gene silencing in a subject, comprising administering to the subject an effective amount of a cell penetrating asymmetric small interfering RNA (cp-asiRNA) or a long-antisense asiRNA (lasiRNA); and an L-type calcium channel blocker comprising cilnidipine, nicardipine, nifedipine, or amlodipine.

2. The method of claim 1 , wherein the cp-asiRNA or lasiRNA and the L-type calcium channel blocker are administered as a single pharmaceutical composition.

3. The method of claim 1 , wherein the cp-asiRNA or lasiRNA, and the L-type calcium channel blocker are administered as separate pharmaceutical compositions.

4. The method of claim 1 , wherein the cp-asiRNA or lasiRNA, and the L-type calcium channel blocker are co-administered.

5. The method of claim 1 , wherein the cp-asiRNA or lasiRNA is administered systemically.

6. The method of claim 1 , wherein the cp-asiRNA or lasiRNA is administered locally.

7. The method of claim 6 , wherein the local administration is to the subject's skin, eyes, or lungs.

8. The method of claim 1 , wherein the L-type calcium channel blocker is administered systemically.

9. The method of claim 1 , wherein the L-type calcium channel blocker is administered locally.

10. The method of claim 9 , wherein the local administration is to the subject's skin, eyes, or lungs.

11. The method of claim 1 , wherein one or both of the cp-asiRNA or lasiRNA, and the L-type calcium channel blocker are formulated for topical, pulmonary, or parenteral delivery.

12. The method of claim 1 , wherein the cp-asiRNA or lasiRNA targets connective tissue growth factor (CTGF) gene.

13. The method of claim 12 , wherein the subject has a CTGF-associated disease or disorder comprising keloid, kidney fibrosis, pachydermatosis, pulmonary fibrosis, hepatic fibrosis, arthritis, renal failure, vasculogenesis-related disorder, or dermatofibrosis.

14. The method of claim 1 , wherein the cp-asiRNA or lasiRNA targets MYD88 gene.

15. The method of claim 14 , wherein the subject has an ocular disease or disorder comprising an as age-related macular degeneration (AMD).

16. The method of claim 15 , wherein the AMD comprises dry or wet AMD.

17. The method of claim 1 , wherein the cp-asiRNA or lasiRNA targets a tyrosinase gene.

18. The method of claim 17 , wherein the cp-asiRNA or lasiRNA is suitable for treating skin diseases or conditions comprising skin whitening, darkening, or scarring, atopic dermatitis, psoriasis, scleroderma, hair loss, or wrinkled skin.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 19, 2019
From: SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION
To: OLIX PHARMACEUTICALS, INC.
Reel/Frame 048936/0159 →
Priority Claims (1)
KR 10-2016-0081914 · Jun 29, 2016 · national
Continuity (1)
Related Publication 20190321388A1 · Oct 24, 2019
Cited By (1)
US 12,686,867