IP Library Granted Patent US 10,105,552
Granted Patent B2
US 10,105,552 · App. 15/386,834 · Granted Oct 23, 2018

Formulations of histone deacetylase inhibitor and uses thereof

Inventors: David J. Loury (Incline Village, NV); Joseph J. Buggy (Mountain View, CA); Tarak D. Mody (Sunnyvale, CA); Erik J. Verner (San Mateo, CA); Norbert Purro (Los Gatos, CA); Sriram Balasubramanian (North Wales, PA)
Assignee: Pharmacyclics LLC
A61N5/10A61K9/205A61K9/2054A61K9/2826A61K9/2846A61K9/2866A61K9/4808A61K9/4858A61K9/4866A61K9/501A61K9/5026A61K31/166A61K31/343A61K31/35A61K31/381A61K31/40A61K31/4184A61K31/47A61K31/497A61K31/573A61K31/69A61K31/704A61K38/05A61K45/05A61K45/06A61K47/02A61K47/12C07D307/85
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Quick Facts
Patent No.
US 10,105,552
App. No.
15/386,834
Granted
Oct 23, 2018
Kind
B2
Abstract

Dosing regimens, methods of treatment, controlled release formulations, and combination therapies that include an HDAC inhibitor, or a pharmaceutically acceptable salt thereof, are described.

Claims (18)

1. A method of treating cancer in a human patient, comprising:

administering to the patient a therapeutically effective amount of Compound 1:

or a pharmaceutically acceptable salt thereof; and

administering to the patient a therapeutically effective amount of rituximab.

2. The method of claim 1 , wherein the cancer is a hematological cancer, a solid tumor, or a sarcoma.

3. The method of claim 1 , wherein the cancer is selected from: breast cancer, colon cancer, colorectal carcinoma, non-small cell lung cancer, small-cell lung cancer, liver cancer, ovarian cancer, prostate cancer, uterine cervix cancer, urinary bladder cancer, gall bladder carcinoma, gastric carcinoma, esophageal cancer, gastrointestinal stromal tumor, pancreatic cancer, germ cell tumors, mast cell tumors, neuroblastoma, retinoblastoma, mesothelioma, mastocytosis, testicular cancers, glioblastomas, astrocytomas, sarcoma, osteosarcoma, B cell lymphoma, T cell lymphoma, NK cell lymphoma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, melanoma, basal cell carcinoma, skin cancer, myeloma, leukemia, acute myelocytic leukemia (AML), acute lymphocytic leukemia (ALL), myelodysplastic syndrome, chronic lymphocytic leukemia (CLL) and chronic myelogenous leukemia (CML).

4. The method of claim 3 , wherein the cancer is a non-Hodgkin's lymphoma.

5. The method of claim 4 , wherein the cancer is an indolent non-Hodgkin's lymphoma.

6. The method of claim 1 , wherein the cancer is a kidney cancer.

7. The method of claim 6 , wherein the cancer is an adenocarcinoma of the kidney.

8. The method of claim 1 , wherein administering to the patient a therapeutically effective amount of Compound 1 comprises orally administering a first dose of Compound 1, and orally administering a second dose of Compound 1, wherein the two doses are administered within the same day.

9. The method of claim 8 , wherein the second dose is administered about 4 to about 6 hours after the first dose.

10. The method of claim 8 , wherein the first and second doses together comprise a total daily dose of from 10 mg/m 2 to 200 mg/m 2 of Compound 1.

11. The method of claim 10 , wherein the first dose is administered as a formulation that includes about 30 mg/m 2 , about 40 mg/m 2 , about 50 mg/m 2 , or about 60 mg/m 2 of Compound 1; and the second dose is administered as a formulation that includes about 30 mg/m 2 , about 40 mg/m 2 , about 50 mg/m 2 , or about 60 mg/m 2 of Compound 1.

12. The method of claim 10 , wherein the first and second doses together comprise a total daily dose of 30 mg/m 2 to 90 mg/m 2 of Compound 1.

13. The method of claim 12 , wherein the total daily dose is about 60 mg/m 2 or about 90 mg/m 2 of Compound 1.

14. The method of claim 8 , wherein administering a therapeutically effective amount of Compound 1 comprises maintaining an effective plasma concentration of the HDAC inhibitor for at least 6 consecutive hours.

15. The method of claim 8 , further comprising orally administering a third dose of Compound 1, wherein the first dose, the second dose and the third dose are administered consecutively about 4 to 6 hours apart.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 2, 2017
From: LOURY, DAVID J.; BUGGY, JOSEPH J.; MODY, TARAK D.; VERNER, ERIK J.; PURRO, NORBERT; BALASUBRAMANIAN, SRIRAM
To: PHARMACYCLICS, INC.
Reel/Frame 041443/0391 →
MERGER Recorded Mar 2, 2017
From: OXFORD AMHERST CORPORATION; PHARMACYCLICS, INC.
To: PHARMACYCLICS, INC.
Reel/Frame 041443/0412 →
MERGER Recorded Mar 2, 2017
From: PHARMACYCLICS, INC.; OXFORD AMHERST LLC
To: PHARMACYCLICS LLC
Reel/Frame 041443/0425 →
Continuity (5)
Continuation 14620075 · Feb 11, 2015
Continuation 14069233 · Oct 31, 2013
Continuation In Part 12761588 · Apr 16, 2010
Provisional Application 61170517 · Apr 17, 2009
Related Publication 20170333731A1 · Nov 23, 2017
Cited By (1)
US 12,245,355