IP Library Granted Patent US 10,603,314
Granted Patent B2
US 10,603,314 · App. 11/883,474 · Granted Mar 31, 2020

Method for treating gefitinib resistant cancer

Inventors: Daniel A. Haber (Chestnut Hill, MA); Daphne Winifred Bell (Chevy Chase, MD); Jeffrey E. Settleman (Newton, MA); Raffaella Sordella (Cold Spring Harbor, NY); Nadia G. Godin-Heymann (Stanmore, GB); Eunice L. Kwak (Marlborough, MA); Sridhar Krishna Rabindran (Eagleville, PA)
Assignees: The General Hospital Corporation; Wyeth LLC
A61K31/4709A61K31/4706A61K38/17
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Quick Facts
Patent No.
US 10,603,314
App. No.
11/883,474
Granted
Mar 31, 2020
Kind
B2
Abstract

The present invention is directed to methods for the treatment of gefitinib and/or erlotinib resistant cancer. An individual with cancer is monitored for cancer progression following treatment with gefitinib and/or erlotinib. Progression of the cancer is indicative that the cancer is resistant to gefitinib and/or erlotinib. Once progression of cancer is noted, the subject is administered a pharmaceutical composition comprising an irreversible epidermal growth factor receptor (EGFR) inhibitor. In preferred embodiments, the irreversible EGFR inhibitor is EKB-569, HKI-272 and HKI-357.

Claims (9)

1. A method for treating gefitinib and/or erlotinib resistant non-small cell lung cancer in a patient in need thereof, comprising administering daily to the patient having gefitinib and/or erlotinib resistant non-small cell lung cancer a pharmaceutical composition comprising a unit dosage of an irreversible epidermal growth factor receptor (EGFR) inhibitor that covalently binds to cysteine 773 residue in the ligand-binding pocket of EGFR or cysteine 805 residue in the ligand-binding pocket of erb-B2.

2. The method of claim 1 , wherein the irreversible EGFR inhibitor is EKB-569 or HKI-357.

3. The method of claim 1 , wherein the irreversible EGFR inhibitor covalently binds to cysteine 773 residue of EGFR.

4. The method of claim 1 , wherein the irreversible EGFR inhibitor covalently binds to cysteine 805 residue of erb-B2.

5. The method of claim 1 , wherein the method further comprises administering at least one other tyrosine kinase inhibitor.

6. The method of claim 1 , wherein the method further comprises administering radiation.

7. The method of claim 1 , wherein the route of administering is intravenous, intramuscular, subcutaneous, intradermal, intraperitoneal, intrathecal, intrapleural, intrauterine, rectal, vaginal, topical, or intratumor.

8. The method of claim 1 , wherein the route of administering is transmucosal or transdermal.

9. The method of claim 1 , wherein the route of administering is oral.

Assignments (3)
CHANGE OF NAME Recorded Sep 24, 2015
From: WYETH
To: WYETH LLC
Reel/Frame 036675/0535 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2008
From: HABER, DANIEL A.; BELL, DAPHNE WINIFRED; SETTLEMAN, JEFFREY E.; SORDELLA, RAFFAELLA; GODIN-HEYMANN, NADIA G.; KWAK, EUNICE L.
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 021142/0445 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2008
From: RABINDRAN, SRIDHAR KRISHNA
To: WYETH
Reel/Frame 021142/0453 →
Continuity (3)
Provisional Application 60649483 · Feb 3, 2005
Provisional Application 60671989 · Apr 15, 2005
Related Publication 20100087482A1 · Apr 8, 2010