Compounds, compositions, and methods for the treatment of inflammatory, degenerative, and neurodegenerative diseases
US-2024409487-A1 · Dec 12, 2024 · US
US9763905B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9763905-B2 |
| Application number | US-201414777485-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 17, 2014 |
| Priority date | Mar 15, 2013 |
| Publication date | Sep 19, 2017 |
| Grant date | Sep 19, 2017 |
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Disclosed herein are compositions and methods for treating or preventing certain cancers in a subject. In certain embodiments such compositions and methods generally relate to the use of G-coupled protein receptor 40 (GPR40) agonists to inhibit the growth or induce apoptosis of certain cancer cells. The compositions and related methods disclosed herein may be used to treat subjects affected by cancers, such as melanoma, medullary thyroid carcinoma, malignant peripheral nerve sheath tumors and neuroblastoma, and to reduce the incidence of metastases in such affected subjects.
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What is claimed is: 1. A method of treating melanoma in a subject affected by melanoma, wherein the method comprises administering a composition to the subject and thereby treating the melanoma, wherein the composition comprises an effective amount of a G-protein coupled receptor 40 (GPR40) agonist; and wherein the GPR40 agonist is not an omega-3 fatty acid, an omega-6 fatty acid, or compound C. 2. The method of claim 1 , wherein the G-protein coupled receptor 40 (GPR40) agonist comprises TAK-875 or a pharmaceutically acceptable salt thereof. 3. The method of claim 1 , wherein the G-protein coupled receptor 40 (GPR40) agonist is selected from the group consisting of GW9508, TAK-875, AMG-837, TUG-469, compound 4p, and pharmaceutically acceptable salts thereof. 4. The method of claim 1 , wherein the method further comprises administering an effective amount of one or more chemotherapeutic agents to the subject. 5. The method of claim 1 , wherein the subject is a mammal. 6. The method of claim 1 , wherein the subject is a human. 7. The method of claim 1 , wherein the composition is administered orally, subcutaneously, topically, or intravenously to the subject.
having one or two double bonds, e.g. oleic, linoleic acids · CPC title
condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone · CPC title
having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids · CPC title
the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil · CPC title
having three or more double bonds, e.g. linolenic (eicosanoids, e.g. leukotrienes A61K31/557) · CPC title
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