IP Library Granted Patent US 10,729,672
Granted Patent B2
US 10,729,672 · App. 13/874,147 · Granted Aug 4, 2020

Antineoplastic combinations with mTOR inhibitor, trastuzumab and/or HKI-272

Inventors: Laurence Moore (Newton, MA); Charles Zacharchuk (Westford, MA); Sridhar K. Rabindran (Chestnut Ridge, NY)
Assignee: Wyeth LLC
A61K31/337A61K31/436A61K31/4709A61K31/4745A61K39/39558A61K45/06
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Quick Facts
Patent No.
US 10,729,672
App. No.
13/874,147
Granted
Aug 4, 2020
Kind
B2
Abstract

A combination of temsirolimus and trastuzumab in the treatment of cancer is provided. A combination of temsirolimus and HKI-272 is provided. A combination of a trastuzumab and a HKI-272 is also provided. Regimens and kits for treatment of metastatic breast cancer, containing trastuzumab, temsirolimus and/or HKI-272, optionally in combination with other anti-neoplastic agents, or immune modulators are described.

Claims (16)

1. A method of treating a HER2+ neoplasm in a patient in need thereof, consisting of administering to the patient:

i) temsirolimus (CCI-779) or a prodrug or pharmaceutically acceptable salt thereof in combination with one or more pharmaceutically acceptable carriers; and

ii) 0.1 to 300 mg of (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or a pharmaceutically acceptable salt thereof, in combination with one or more pharmaceutically acceptable carriers.

2. The method of claim 1 , wherein the temsirolimus (CCI-779) and (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, are administered in subtherapeutically effective amounts.

3. The method of claim 1 , wherein the neoplasm is selected from the group consisting of: lung cancer, including bronchioalveolar carcinoma and non small cell lung cancer; breast cancer; myeloma; prostate cancer; head and neck cancer; transitional cell carcinoma; and small cell and large cell neuroendocrine carcinoma of the uterine cervix.

4. The method of claim 3 , wherein the breast cancer is metastatic breast cancer.

5. The method of claim 1 , wherein the temsirolimus (CCI-779) and (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, are administered simultaneously, separately, sequentially, or in a staggered regimen to the patient.

6. The method of claim 1 , wherein the temsirolimus (CCI-779) and (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, are administered to the patient in a formulation suitable for one or more of the following administration routes: oral, as an aerosol, parenteral, intraperitoneal, transdermal, or as a suppository.

7. The method of claim 1 , wherein the temsirolimus (CCI-779) and (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, are administered to the patient using the same route of administration or using different routes of administration.

8. The method of claim 1 , wherein the temsirolimus (CCI-779) and (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, are contained in a pharmaceutical pack or kit.

9. The method of claim 1 , wherein the temsirolimus (CCI-779) is administered orally or intravenously.

10. The method of claim 9 , wherein an amount in the range of between 10 mg to 250 mg of the temsirolimus (CCI-779) is administered orally to the patient per week.

11. The method of claim 9 , wherein an amount in the range of between 5 mg to 175 mg of the temsirolimus (CCI-779) is administered intravenously to the patient per week.

12. The method of claim 11 , wherein the (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, is administered orally.

13. The method of claim 12 , wherein the (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, is administered daily.

14. The method of claim 13 , wherein an amount of 80 mg, 160 mg, or 240 mg of the (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide, or pharmaceutically acceptable salt thereof, is administered orally.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2014
From: MOORE, LAURENCE; ZACHARCHUK, CHARLES; RABINDRAN, SRIDHAR K.
To: WYETH
Reel/Frame 033090/0805 →
CHANGE OF NAME Recorded Jun 12, 2014
From: WYETH
To: WYETH LLC
Reel/Frame 033136/0667 →
Continuity (6)
Continuation 13454768 · Apr 24, 2012
Continuation 12539914 · Aug 12, 2009
Division 11592066 · Nov 2, 2006
Provisional Application 60837509 · Aug 14, 2006
Provisional Application 60733562 · Nov 4, 2005
Related Publication 20140050721A1 · Feb 20, 2014