IP Library Granted Patent US 11,382,877
Granted Patent B2
US 11,382,877 · App. 16/604,978 · Granted Jul 12, 2022

Formulation of (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone with enhanced stability and bioavailability

Inventor: Manoj Maniar (Fremont, CA)
Assignee: ONCONOVA THERAPEUTICS, INC.
A61K31/145A61K9/0053A61K9/4858A61K47/10A61P35/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,382,877
App. No.
16/604,978
Granted
Jul 12, 2022
Kind
B2
Abstract

Pharmaceutical compositions of (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone and pharmaceutically acceptable salts thereof are described as well as methods of their use, and a dose regimen of (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone, sodium salt to reduce the incidence of urothelial toxicity.

Claims (18)

1. A pharmaceutical composition comprising,

a) (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone and pharmaceutically acceptable salts thereof,

b) basic pre-treated low molecular weight polyethylene glycol comprising one or more of PEG 200, PEG 300, PEG 400, PEG 600, and/or PEG 800;

c) undiluted pH of about 11.0 to about 14.0; and

d) less than 5% water or aqueous solution.

2. An oral dosage form comprising the pharmaceutical composition of claim 1 having about 35 to about 400 mg of (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone, sodium salt in each oral dosage form.

3. A method of treating conditions mediated by abnormal cell proliferation comprising administering an effective amount of the pharmaceutical composition of claim 1 to a subject in need thereof.

4. The method of claim 3 wherein said condition is selected from hematological cancer.

5. The method of claim 4 wherein said hematological cancer is selected from AML and MDS.

6. The method of claim 5 , wherein said pharmaceutical composition is in an oral dosage form comprising 70 mg to 280 mg (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone, sodium salt per dosage form.

7. The method of claim 6 , wherein said pharmaceutical composition is in an oral dosage form comprising 280 mg (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone, sodium salt per dosage form and said oral dosage form is administered in a dose of about 280 mg to 840 mg twice per day to said subject.

8. A method of treating conditions mediated by abnormal cell proliferation comprising administering an effective amount of (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone, sodium salt to a patient in need thereof, comprising orally administering a first dose of 70-840 mg approximately 1-2 hours before breakfast, and a second dose of 70-560 mg administered in the fasting state about 6 to about 8 hours after the first dose.

9. The method of claim 8 wherein said patient is administered (E)-2,4,6-trimethoxystyryl-3-[(carboxymethyl)amino]-4-methoxybenzylsulphone, sodium salt for three weeks followed by one week off and said patient is also administered azacitidine starting at day 8 for one week.

10. The method of claim 8 wherein said condition is a hematological cancer.

11. The method of claim 10 wherein said hematological cancer is selected from the group consisting of AML and MDS.

12. The method of claim 8 wherein the first dose is selected from 70 mg, 140 mg, 280 mg, 560 mg, 700 mg, and 840 mg, and the second dose is selected from 70 mg, 140 mg, 280 mg, and 560 mg.

13. The method of claim 12 wherein the first dose is selected from 280 mg, 560 mg, and 840 mg, and the second dose is selected from the group selected from 280, and 560 mg, and said condition is a hematological cancer.

14. The method of claim 8 wherein the first dose is 840 mg and the second dose is 280 mg, or wherein the first dose is 560 mg and the second dose is 280-560 mg.

Assignments (2)
CHANGE OF NAME Recorded Oct 4, 2024
From: ONCONOVA THERAPEUTICS, INC.
To: TRAWS PHARMA, INC.
Reel/Frame 069121/0647 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2019
From: MANIAR, MANOJ
To: ONCONOVA THERAPEUTICS, INC.
Reel/Frame 050715/0312 →
Continuity (4)
Continuation In Part 15688320 · Aug 28, 2017
Continuation In Part PCTUS2017048890 · Aug 28, 2017
Provisional Application 62485355 · Apr 13, 2017
Related Publication 20210186902A1 · Jun 24, 2021