Transgenic animals capable of being induced to delete senescent cells
US-9968076-B2 · May 15, 2018 · US
US10588916B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10588916-B2 |
| Application number | US-201816160840-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 15, 2018 |
| Priority date | Oct 31, 2017 |
| Publication date | Mar 17, 2020 |
| Grant date | Mar 17, 2020 |
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This invention is based on the discovery that many eye conditions associated with aging are mediated at least in part by cells bearing a senescent phenotype. Senescent cells accumulate with age, and express factors that contribute to the pathophysiology of age related conditions. The data show that in age-matched patients, the severity of age-related conditions correlates with the abundance of senescent cells, and that clearing senescent cells can help abrogate the condition. Small molecule drugs that remove senescent cells from affected tissue in the eye are provided that have special efficacy in treating ophthalmic conditions. They not only inhibit progression of the disease, they can also reverse some of the pathophysiology—such as neovascularization and vaso-obliteration—that lead to vision loss. These senolytic agents have an appropriate dose and specificity profile to be effective in the clinical management of previously intractable ophthalmic conditions.
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The invention claimed is: 1. A method of inhibiting vaso-obliteration that leads to vision loss in an eye of a subject in need thereof, comprising administering to the eye a pharmaceutical composition comprising an effective amount of a compound, wherein the compound is BM-1197. 2. The method of claim 1 , wherein the amount of the compound in the pharmaceutical composition that is administered to the eye is also effective in inhibiting pathogenic angiogenesis in the eye. 3. The method of claim 1 , wherein the amount of the compound in the pharmaceutical composition that is administered to the eye is also effective in inhibiting retinal neovascularization in the eye. 4. The method of claim 1 , wherein the amount of the compound in the pharmaceutical composition that is administered to the eye is also effective in inhibiting retinal or choroidal vascular leakage in the eye. 5. The method of claim 1 , wherein the amount of the compound in the pharmaceutical composition that is administered to the eye is also effective in promoting repair of functional vasculature in the eye.
Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin · CPC title
Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers · CPC title
Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · CPC title
Ophthalmic agents · CPC title
Eye, e.g. artificial tears · CPC title
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