IP Library Granted Patent US 9,211,262
Granted Patent B2
US 9,211,262 · App. 12/964,861 · Granted Dec 15, 2015

Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity

Inventors: Alberto Bernareggi (Concorezzo, IT); Valeria Livi (Monza, IT)
Assignee: CTI BioPharma Corp.
A61K9/19A61K9/0019A61K47/02A61K47/26A61K47/36
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Quick Facts
Patent No.
US 9,211,262
App. No.
12/964,861
Granted
Dec 15, 2015
Kind
B2
Abstract

Injectable pharmaceutical compositions containing 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate as active ingredient in the form of a lyophilized powder with a carrier selected from lactose and dextran, mixed with sodium chloride.

Claims (14)

1. A pharmaceutical composition, comprising 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate and a lactose carrier mixed with sodium chloride, wherein the weight ratio between the carrier and sodium chloride is between 1:1 and 3:1,

and wherein the composition is in lyophilized form.

2. The composition according to claim 1 , further comprising an antioxidant.

3. The composition according to claim 1 , wherein the weight ratio between 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate and the carrier is between 1:2 and 1:6.

4. The composition according to claim 1 , wherein 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate is in a unit dose of between 25 and 200 mg.

5. The composition according to claim 4 , wherein the unit dose of 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate is 50 mg.

6. The composition according to claim 1 , further comprising a sterile solvent suitable to reconstitute the lyophilisate and suitable for parenteral administration.

7. A process for preparing the composition according to claim 1 , the process comprising:

lyophilizing an aqueous solution of 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate in the presence of lactose and sodium chloride wherein the step of lyophilizing comprises:

freezing the solution at a temperature below at least −45° C. for at least 3 hours;

drying the frozen solution to form a product, by increasing the temperature of the frozen solution to −35° C.±5° C. in approximately 3 hours and maintaining said temperature for at least 40 hours; and

then drying the product by increasing the temperature of the product to +30° C.±5° C. in 10 hours and maintaining said temperature for at least 8 hours.

8. A composition, comprising an aqueous solution comprising 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate and a) a lactose carrier mixed with sodium chloride, wherein the concentration of 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate is 7-15 mg/ml, and wherein the weight ratio between the lactose carrier and sodium chloride is between 1:1 and 3:1.

9. The composition according to claim 8 , comprising 10 to 40 mg/ml of sodium chloride and 20 to 60 mg/ml of lactose.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2020
From: CTI BIOPHARMA CORP.; CTI LIFE SCIENCES
To: LES LABORATOIRES SERVIER
Reel/Frame 052353/0084 →
CHANGE OF NAME Recorded Nov 9, 2015
From: CELL THERAPEUTICS, INC.
To: CTI BIOPHARMA CORP.
Reel/Frame 037076/0727 →
MERGER Recorded Aug 13, 2012
From: CELL THERAPEUTICS EUROPE, S.R.L.
To: CELL THERAPEUTICS, INC.
Reel/Frame 028774/0361 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2011
From: BERNAREGGI, ALBERTO; LIVI, VALERIA
To: CELL THERAPEUTICS EUROPE S.R.L.
Reel/Frame 025961/0263 →
Priority Claims (1)
IT MI2002A1040 · May 16, 2002 · national
Continuity (2)
Continuation 10514301
Related Publication 20110144147A1 · Jun 16, 2011