Atherosclerosis-targeted liposome nanocarrier delivery system and preparation method therefor
US-2024424132-A1 · Dec 26, 2024 · US
US9526710B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9526710-B2 |
| Application number | US-201414486477-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 15, 2014 |
| Priority date | Aug 13, 2012 |
| Publication date | Dec 27, 2016 |
| Grant date | Dec 27, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention discloses novel agents and methods for diagnosis and treatment of melanoma. Also disclosed are related arrays, kits, and screening methods.
Opening claim text (preview).
What is claimed is: 1. A method of treating metastatic melanoma in a subject in need thereof, said method comprising administering to the subject an LXRβ agonist selected from: or a pharmaceutically acceptable salt thereof in an amount sufficient to suppress metastatic progression of said melanoma. 2. The method of claim 1 , wherein said metastatic melanoma is resistant to vemurafenib and/or dacarbazine. 3. The method of claim 1 , wherein said LXRβ agonist is compound 1, or a pharmaceutically acceptable salt thereof. 4. The method of claim 1 , wherein said LXRβ agonist is compound 2, or a pharmaceutically acceptable salt thereof. 5. The method of claim 1 , wherein said LXRβ agonist is compound 12, or a pharmaceutically acceptable salt thereof. 6. The method of claim 1 , wherein said LXRβ agonist is compound 25, or a pharmaceutically acceptable salt thereof. 7. The method of claim 1 , wherein said metastatic melanoma is resistant to dacarbazine, a BRAF inhibitor, a MEK inhibitor, a CTLA-4 inhibitor, a PD-1 inhibitor and/or a PD-L1 inhibitor. 8. The method of claim 1 , wherein the method does not comprise further concurrently administering to the subject an antiproliferative agent. 9. The method of claim 1 , wherein said method further comprises administration of an additional anticancer therapy. 10. The method of claim 9 , wherein said additional anticancer therapy is an antiproliferative. 11. The method of claim 10 , wherein said antiproliferative is a PD1 inhibitor, a VEGF inhibitor, a VEGFR2 inhibitor, a CTLA4 inhibitor, and/or a PDL1 inhibitor. 12. The method of claim 10 , wherein said antiproliferative is a PD-1 inhibitor or a PD-L1 inhibitor. 13. The method of claim 10 , wherein said antiproliferative is nivolumab, ipilmumab, dacarbazine, or vemurafenib. 14. The method of claim 1 , wherein said method comprises suppressing metastatic colonization of the melanoma to the lung and/or the brain.
Related publications grouped by family.
Answers are generated from the same data shown on this page.