IP Library Granted Patent US 9,283,208
Granted Patent B2
US 9,283,208 · App. 14/117,456 · Granted Mar 15, 2016

Medicaments and methods for treating cancer

Inventor: Hooshmand Sheshbaradaran (Hoboken, NJ)
Assignee: NIIKI PHARMA INC.
A61K31/416A61K9/0019A61K9/19A61K31/573A61K45/06
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Quick Facts
Patent No.
US 9,283,208
App. No.
14/117,456
Granted
Mar 15, 2016
Kind
B2
Abstract

Medicaments and methods for treating cancer are disclosed.

Claims (12)

1. A method of treating neuroendocrine cancer, comprising administering to a patient in need thereof, a pharmaceutical unit dosage form comprising greater than about 500 mg of sodium trans-[tetrachlorobis(1H-indazole)ruthenate (III)]and is substantially free of indazolium hydrochloride wherein the dosage form is administered to the patient intravenously on a dosing schedule of once a week.

2. The method of claim 1 , wherein the patient is administered the dosage form once on each day 1, day 8 and day 15 of a 28-day or monthly cycle.

3. The method of claim 2 , wherein the dosage form is administered at an amount of at least about 320 mg/m 2 based on the body surface area of said patient.

4. The method of claim 3 , wherein the dosage form is administered at an amount of from about 320 mg/m 2 to about 625 mg/m 2 based on the body surface area of said patient.

5. The method of claim 1 , further comprising the step of administering to the patient a medication for preventing infusional fever prior to the administration of the dosage form.

6. The method of claim 5 , wherein the medication for preventing infusional fever is a steroid.

7. The method of claim 6 , wherein said steroid is prednisone or dexamethasone.

8. The method of claim 1 , wherein the patient plasma C max is less than about 50 μg/mL.

9. The method of claim 1 , wherein said cancer is associated with a solid tumor refractory to treatment.

10. The method of claim 1 , wherein the treating results in stable disease in the patient.

11. The method of claim 1 , wherein the pharmaceutical unit dosage form comprises from about 600 to about 1000 mg of sodium trans-[tetrachlorobis(1H-indazole)ruthenate (III)] and is substantially free of indazolium hydrochloride.

12. The method of claim 1 , wherein said unit dosage form is a kophilized powder in a vial.

Assignments (3)
MERGER Recorded Nov 10, 2015
From: NIIKI PHARMA ACQUISTION CORP. 2
To: INTEZYNE TECHNOLOGIES, INC.
Reel/Frame 037080/0048 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2015
From: SHESHBARADARAN, HOOSHMAND
To: NIIKI PHARMA INC.
Reel/Frame 035414/0016 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2014
From: SHESHBARADARAN, HOOSHMAND
To: INTEZYNE TECHNOLOGIES, INC.
Reel/Frame 034184/0506 →
Continuity (2)
Provisional Application 61486783 · May 17, 2011
Related Publication 20150080354A1 · Mar 19, 2015