IP Library Granted Patent US 9,139,658
Granted Patent B2
US 9,139,658 · App. 12/978,275 · Granted Sep 22, 2015

Medicament for treatment cancer

Inventors: Toshihiro Noguchi (Osaka, JP); Akemi Baba (Minoh, JP); Mitsuharu Hanada (Ibaraki, JP)
Assignee: SUMITOMO DAINIPPON PHARMA CO., LTD.
C07K16/32A61K39/395A61K39/39558A61K31/7036A61K2039/505A61K2039/545
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Quick Facts
Patent No.
US 9,139,658
App. No.
12/978,275
Granted
Sep 22, 2015
Kind
B2
Abstract

A medicament for treating cancer for use in combination therapy with an anti-HER2 antibody, which comprises amrubicin or a pharmaceutically acceptable salt thereof as an active ingredient.

Claims (9)

1. A method of treating breast cancer, which is a breast cancer in which HER2 is highly expressed, comprising administering a first composition including an effective amount of amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof and a second composition including an effective amount of trastuzumab.

2. The method according to claim 1 , comprising administering amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof at 0.5-3.0 mg/kg/day and administering trastuzumab at 0.1-4.5 mg/kg/day.

3. The method according to claim 2 , comprising administering amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof on successive three days in every three weeks, while administering trastuzumab every one week.

4. The method according to claim 1 , comprising administering amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof at 1.5-9.0 mg/kg/day and administering trastuzumab at 0.1-4.5 mg/kg/day.

5. The method according to claim 4 , comprising administering amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof every three weeks, while administering trastuzumab every one week.

6. The method according to claim 2 , wherein a dosage ratio of amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof and trastuzumab is 2:1-8:1 at one week after initiating the administration of both agents.

7. The method according to claim 3 , wherein a dosage ratio of amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof and trastuzumab is 2:1-8:1 at one week after initiating the administration of both agents.

8. The method according to claim 4 , wherein a dosage ratio of amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof and trastuzumab is 2:1-8:1 at one week after initiating the administration of both agents.

9. The method according to claim 5 , wherein a dosage ratio of amrubicin, amrubicinol, or a pharmaceutically acceptable salt thereof and trastuzumab is 2:1-8:1 at one week after initiating the administration of both agents.

Assignments (1)
CHANGE OF NAME Recorded Aug 25, 2014
From: DAINIPPON SUMITOMO PHARMA CO., LTD.
To: SUMITOMO DAINIPPON PHARMA CO., LTD.
Reel/Frame 033609/0366 →
Priority Claims (1)
JP 2000-228239 · Jul 28, 2000 · national
Continuity (3)
Continuation 11761264 · Jun 11, 2007
Division 10333978
Related Publication 20110104160A1 · May 5, 2011