IP Library Granted Patent US 8,431,566
Granted Patent B2
US 8,431,566 · App. 13/250,080 · Granted Apr 30, 2013

Cyclopamine lactam analogs and methods of use thereof

Inventors: Alfredo Castro (Winchester, MA); Michael J. Grogan (Winchester, MA); Andre Lescarbeau (Somerville, MA); Martin Tremblay (Melrose, MA)
Assignee: Infinity Discovery, Inc.
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Quick Facts
Patent No.
US 8,431,566
App. No.
13/250,080
Granted
Apr 30, 2013
Kind
B2
Abstract

The present invention relates to steroidal alkaloids useful in the treatment of hedgehog pathway related disorders, particularly cancer.

Claims (26)

1. A compound of the formula:

or a pharmaceutically acceptable salt thereof.

2. A pharmaceutical composition comprising a compound of the formula:

or a pharmaceutically acceptable salt thereof and at least one pharmaceutically acceptable excipient.

3. A method of treating cancer, which comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt thereof; wherein the cancer is selected from the group consisting of acute lymphocytic leukemia, acute myelocytic leukemia, basal cell carcinoma, bile duct carcinoma, bladder carcinoma, breast cancer, chondrosarcoma, chronic lymphocytic leukemia, chronic myeloid leukemia, colon cancer, esophageal cancer, gastric cancer, gastrointestinal stromal tumor, glioma, hepatocellular cancer, Hodgkin's disease, leukemia, lung cancer, medulloblastoma, melanoma, multiple myeloma, myelodysplastic syndrome, neuroectodermal tumors, non-Hodgkin's type lymphoma, osteogenic sarcoma, ovarian cancer, pancreatic cancer, prostate cancer, sarcoma, and testicular cancer.

4. The method of claim 3 , wherein the cancer is selected from the group consisting of acute lymphocytic leukemia, basal cell carcinoma, breast cancer, chondrosarcoma, chronic lymphocytic leukemia, chronic myeloid leukemia, colon cancer, esophageal cancer, gastric cancer, glioma, hepatocellular cancer, lung cancer, medulloblastoma, multiple myeloma, non-Hodgkin's type lymphoma, osteogenic sarcoma, ovarian cancer, pancreatic cancer, and prostate cancer.

5. The method of claim 3 , wherein the cancer is pancreatic cancer.

6. The method of claim 3 , wherein the cancer is chondrosarcoma.

7. The method of claim 3 , wherein the cancer is lung cancer.

8. The method of claim 7 , wherein the lung cancer selected from the group consisting of small cell lung cancer and non-small cell lung cancer.

9. The method of claim 3 , wherein the cancer is basal cell carcinoma.

10. The method of claim 3 , wherein the cancer is medulloblastoma.

11. The method of claim 3 , wherein the cancer is ovarian cancer.

12. The method according to claim 3 , wherein the cancer is osteogenic sarcoma.

13. The method of claim 3 , wherein the cancer is selected from the group consisting of acute lymphocytic leukemia, acute myelocytic leukemia, chronic lymphocytic leukemia, chronic myeloid leukemia, Hodgkin's disease, leukemia, multiple myeloma, myelodysplastic syndrome, and non-Hodgkin's type lymphoma.

14. The method of claim 3 , wherein the cancer is selected from the group consisting of acute lymphocytic leukemia, acute myelocytic leukemia, chronic myelocytic leukemia, and chronic lymphocytic leukemia.

15. The method of claim 3 , wherein the compound or pharmaceutically acceptable salt thereof is used in combination with one or more chemotherapeutic or other anti-cancer agent.

16. The method of claim 15 , wherein the other anti-cancer agent is radiation.

17. The method of claim 3 , wherein the compound is administered locally to a tumor.

18. The method of claim 3 , wherein the compound is administered systemically.

19. The method of claim 3 , wherein the mode of administration of said compound is inhalation, oral, intravenous, sublingual, ocular, transdermal, rectal, vaginal, topical, intramuscular, intraperitoneal, epidural, subcutaneous, buccal, or nasal.

20. The method of claim 19 , wherein the mode of administration is oral, intravenous, or topical.

21. A method of inhibiting activation of a hedgehog pathway in a patient diagnosed with a hyperproliferative disorder, comprising administering to the patient a compound, or a pharmaceutically acceptable salt thereof, as claimed in claim 1 in an amount sufficient to reduce the activation of the hedgehog pathway in a cell of the patient.

22. The method of claim 21 , wherein said hyper proliferative disorder is cancer.

23. A method of antagonizing the hedgehog pathway in a subject, the method comprising administering to the subject an effective amount of a compound, or a pharmaceutically acceptable salt thereof, as claimed in claim 1 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2020
From: INFINITY PHARMACEUTICALS, INC.
To: ROYALTY SECURITY, LLC
Reel/Frame 051519/0511 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 29, 2011
From: CASTRO, ALFREDO C.; GROGAN, MICHAEL J.; LESCARBEAU, ANDRE; TREMBLAY, MARTIN
To: INFINITY DISCOVERY, INC.
Reel/Frame 027458/0459 →
Continuity (4)
Continuation 13102395 · May 6, 2011
Division 12044878 · Mar 7, 2008
Provisional Application 60893591 · Mar 7, 2007
Related Publication 20120083484A1 · Apr 5, 2012