IP Library Granted Patent US 10,557,850
Granted Patent B2
US 10,557,850 · App. 14/566,436 · Granted Feb 11, 2020

Anti-CXCR1 compositions and methods

Inventors: Max S. Wicha (Ann Arbor, MI); Christophe Ginestier (Marseilles, FR)
Assignee: THE REGENTS OF UNIVERSITY OF MICHIGAN
G01N33/57492A61K31/18A61K31/337A61K45/06G01N33/574G01N33/5743G01N33/57407G01N33/57415G01N33/57434G01N33/57449G01N2333/7158
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Quick Facts
Patent No.
US 10,557,850
App. No.
14/566,436
Granted
Feb 11, 2020
Kind
B2
Abstract

The present invention provides methods of treating cancer by administering an IL8-CXCR1 pathway inhibitor (e.g., an anti-CXCR1 antibody or Repertaxin) alone or in combination with an additional chemotherapeutic agent such that non-tumorigenic and tumorigenic cancer cells in a subject are killed. The present invention also provides compositions and methods for detecting the presence of and isolating solid tumor stem cells in a patient (e.g., based on the presence of CXCR1 or FBXO21).

Claims (18)

1. A method of treating a human subject diagnosed with ER-negative breast cancer, comprising:

(a) administering a pharmaceutical composition containing an effective concentration of Compound 1 to the human subject in need of said treatment, wherein Compound 1 is:

and

(b) administering an effective concentration of paclitaxel to the subject in need of said treatment.

2. The method of claim 1 in which Compound 1 is administered at a dose between 3 and 60 mg per kg.

3. A method of treating a human subject diagnosed with metastatic ER-negative breast cancer, comprising:

(a) administering a pharmaceutical composition containing an effective concentration of Compound 1 to the human subject in need of said treatment, wherein Compound 1 is:

and

(b) administering an effective concentration of paclitaxel to the human subject in need thereof.

4. The method of claim 3 , in which Compound 1 is administered at a dose between 3 and 60 mg per kg.

5. The method of claim 1 , wherein Compound 1 is administered concurrently with paclitaxel.

6. The method of claim 1 , wherein Compound 1 is administered at a time prior to the administration of paclitaxel.

7. The method of claim 1 , wherein Compound 1 is administered at a time subsequent to the administration of paclitaxel.

8. The method of claim 3 , wherein Compound 1 is administered concurrently with paclitaxel.

9. The method of claim 3 , wherein Compound 1 is administered at a time prior to the administration of paclitaxel.

10. The method of claim 3 , wherein Compound 1 is administered at a time subsequent to the administration of paclitaxel.

11. The method of claim 3 , wherein the method results in a reduction of metastasis.

12. The method of claim 3 , wherein Compound 1 is administered orally.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 12, 2017
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042353/0086 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2015
From: WICHA, MAX S.; GINESTIER, CHRISTOPHE
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 035023/0578 →
Continuity (3)
Continuation 12616579 · Nov 11, 2009
Provisional Application 61113458 · Nov 11, 2008
Related Publication 20150094362A1 · Apr 2, 2015