IP Library Granted Patent US 8,822,526
Granted Patent B2
US 8,822,526 · App. 12/600,019 · Granted Sep 2, 2014

Synergistic pharmaceutical combination for the treatment of cancer

Inventors: Maggie Rathos (Mumbai, IN); Kalpana Joshi (Mumbai, IN); Harshal Khanwalkar (Mumbai, IN); Somesh Sharma (Mumbai, IN)
Assignee: Piramal Enterprises Limited
A61K31/704A61K31/4025A61K31/7068A61K31/337A61K45/06
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Quick Facts
Patent No.
US 8,822,526
App. No.
12/600,019
Granted
Sep 2, 2014
Kind
B2
Abstract

A novel pharmaceutical combination comprising a cytotoxic antineoplastic agent selected from a the group consisting of paclitaxel, docetaxel, doxorubicin and gemcitabine or a pharmaceutically acceptable salt thereof and at least one cyclin dependent kinase (CDK) inhibitor; wherein the said combination exhibits synergistic effects when used in the treatment of cancer. The invention also relates to a method for the treatment of cancer, using a therapeutically effective amount of the said combination.

Claims (20)

1. A method of treating a subject in need of treatment for pancreatic cancer, comprising:

administering:

a therapeutically effective amount of a cytotoxic antineoplastic agent, wherein the cytotoxic antineoplastic agent is gemcitabine or a pharmaceutically acceptable salt thereof; in combination with

a therapeutically effective amount of a CDK inhibitor or an enantiomer or a pharmaceutically acceptable salt thereof;

wherein said CDK inhibitor is represented by the formula:

wherein the cytotoxic antineoplastic agent is administered prior to the CDK inhibitor.

2. The method of claim 1 ;

wherein the combination exhibits therapeutic synergy.

3. The method of claim 1 ;

wherein the CDK inhibitor represented by compound of formula I is (+)-trans-2-(2-Chloro-phenyl)-5,7-dihydroxy-8-(2-hydroxymethyl-1-methyl-pyrrolidin-3-yl)-chromen-4-one or its pharmaceutically acceptable salt.

4. The method of claim 1 ;

wherein the administration of the combination results in a synergistic increase in apoptosis.

5. The method of claim 1 ;

wherein the CDK inhibitor is a compound of formula I wherein the phenyl group is substituted by 1, 2, or 3 identical or different substituents selected from:

halogen selected from chlorine, bromine, fluorine, and iodine; and

C 1 -C 4 alkyl and trifluoromethyl.

6. The method of claim 5 ;

wherein the CDK inhibitor is a compound of formula I wherein the phenyl group is substituted by 1, 2, or 3 halogens selected from chlorine, bromine, fluorine, and iodine.

7. The method of claim 6 ;

wherein the CDK inhibitor is a compound of formula I wherein the phenyl group is substituted by chlorine.

Assignments (3)
CHANGE OF NAME Recorded Dec 19, 2012
From: PIRAMAL HEALTHCARE LIMITED
To: PIRAMAL ENTERPRISES LIMITED
Reel/Frame 029501/0861 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2012
From: PIRAMAL LIFE SCIENCES LIMITED
To: PIRAMAL HEALTHCARE LIMITED
Reel/Frame 028527/0874 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2010
From: RATHOS, MAGGIE; JOSHI, KALPANA; KHANWALKAR, HARSHAL; SHARMA, SOMESH
To: PIRAMAL LIFE SCIENCES, LIMITED
Reel/Frame 024930/0947 →
Continuity (1)
Related Publication 20100305057A1 · Dec 2, 2010