IP Library Granted Patent US 8,685,394
Granted Patent B2
US 8,685,394 · App. 13/384,900 · Granted Apr 1, 2014

Combination of anti-CTLA4 antibody with diverse therapeutic regimens for the synergistic treatment of proliferative diseases

Inventor: Maria Jure-Kunkel (Plainsboro, NJ)
Assignee: Bristol-Myers Squibb Company
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Quick Facts
Patent No.
US 8,685,394
App. No.
13/384,900
Granted
Apr 1, 2014
Kind
B2
Abstract

Compositions and methods are disclosed which are useful of the treatment and prevention of proliferative disorders. Such Compositions comprise inter alia an anti-CTLA-4 agent, e.g. ipilimumab or tremelimumab in combination with other chemotherapeutic agents such as dasatinib, imatinib, paclitaxel, gemcitabine, cisplatin or etoposide.

Claims (10)

1. A method for the treatment of cancer, consisting of the administration to a mammal in need thereof a synergistic, therapeutically effective amount of an anti-CTLA-4 antibody, in addition to one or more diluents, vehicles, excipients, and/or inactive ingredients, at a dose ranging from about 3 mg/kg to about 10 mg/kg; with the chemotherapeutic agent 4′-Demethylepipodophyllotoxin 9-[4,6-O-(R)-ethylidene-β-D-glucopyranoside], 4′-(dihydrogen phosphate), or a pharmaceutically acceptable salt, solvate, or hydrate thereof, at a dose of 100 mg/kg; wherein said treatment is sufficient to synergistically reduce tumor burden, produce tumor regression, or reduce tumor development of said cancer.

2. The method according to claim 1 wherein the anti-CTLA-4 antibody is selected from the group consisting of: ipilimumab and tremelimumab.

3. The method according to claim 1 , wherein said anti-CTLA-4 antibody is ipilimumab.

4. The method according to claim 1 , wherein said cancer is a solid tumor.

5. The method according to claim 4 , wherein said solid tumor is selected from the group consisting of: lung cancer, sarcoma, fibrosarcoma, pancreatic cancer, prostate cancer, and colon cancer.

6. The method according to claim 1 , wherein said method is for the treatment of a tumor refractory to said chemotherapeutic agent.

7. The method according to claim 1 , wherein said chemotherapeutic agent is administered before the administration of said anti-CTLA4 antibody.

8. The method according to claim 1 , wherein said chemotherapeutic agent is administered essentially simultaneously with the administration of said anti-CTLA4 antibody.

9. The method according to claim 1 , wherein said chemotherapeutic agent is administered daily.

10. The method according to claim 1 , wherein said anti-CTLA4 antibody is administered about every three weeks.

Continuity (5)
Continuation In Part 12462168 · Jul 30, 2009
Continuation In Part PCTUS2009052209 · Jul 30, 2009
Provisional Application 61085466 · Aug 1, 2008
Provisional Application 61226910 · Jul 20, 2009
Related Publication 20120121604A1 · May 17, 2012