US2019298742A1PendingUtilityA1
Methods of treating cancer
Assignee: INTERCEPT PHARMACEUTICALS INCPriority: Apr 13, 2016Filed: Jun 17, 2019Published: Oct 3, 2019
Est. expiryApr 13, 2036(~9.7 yrs left)· nominal 20-yr term from priority
Inventors:Antonio MoschettaJesus Maria Banales AsurmediLuis Bujanda Fernández De PierolaMaría Jesús Perugorria MontielOihane Erice Azparren
A61K 47/542A61K 47/54A61K 31/133A61P 35/00A61K 47/64A61K 2039/505A61K 31/575
45
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Claims
Abstract
The present invention relates to methods of treating or preventing cancer in a subject in need thereof comprising administering a therapeutically effective amount of a compound of the invention.
Claims
exact text as granted — not AI-modified1 . A method of treating or preventing cancer in a subject in need thereof comprising administering a therapeutically effective amount of a FXR agonist selected from Compound 1 or 2:
or a pharmaceutically acceptable salt or amino acid conjugate thereof.
2 . The method of claim 1 , wherein the cancer is selected from hepatocellular carcinoma, pancreatic cancer, kidney cancer, prostate cancer, esophageal cancer, breast cancer, gastric cancer, renal cancer, salivary gland cancer, ovarian cancer, uterine body cancer, bladder cancer, and lung cancer.
3 . The method of claim 1 or 2 , wherein the cancer is hepatocellular carcinoma.
4 . The method of claim 3 , wherein the hepatocellular carcinoma is selected from the group consisting of early stage hepatocellular carcinoma, non-metastatic hepatocellular carcinoma, primary hepatocellular carcinoma, advanced hepatocellular carcinoma, locally advanced hepatocellular carcinoma, metastatic hepatocellular carcinoma, hepatocellular carcinoma in remission, or recurrent hepatocellular carcinoma.
5 . The method of any one of claims 1 - 4 , wherein the FXR agonist is Compound 1 or a pharmaceutically acceptable salt thereof.
6 . The method of claim 5 , wherein the FXR agonist is the sodium salt of Compound 1.
7 . The method of claim 5 , wherein the FXR agonist is the N,N-diethaneamine salt of Compound 1.
8 . The method of any one of claims 1 - 4 , wherein the FXR agonist is Compound 2 or a pharmaceutically acceptable salt or amino acid conjugate thereof.
9 . The method of claim 8 , wherein the FXR agonist is the glycine conjugate of Compound 2.
10 . The method of claim 8 , wherein the FXR agonist is the taurine conjugate of Compound 2.
11 . The method of claim 8 , wherein the FXR agonist is the sarcosine conjugate of Compound 2.
12 . A pharmaceutical composition comprising a FXR agonist selected from Compound 1 or 2:
or a pharmaceutically acceptable salt or amino acid conjugate thereof, for treating or preventing cancer in a subject in need thereof and a pharmaceutically acceptable excipient.
13 . A kit for treating or preventing cancer in a subject in need thereof comprising Compound 1 or Compound 2:
or a pharmaceutically acceptable salt or amino acid conjugate thereof.
14 . Use of a FXR agonist selected from Compound 1 or 2:
or a pharmaceutically acceptable salt or amino acid conjugate thereof in the manufacture of a medicament for treating or preventing cancer in a subject in need thereof.Join the waitlist — get patent alerts
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