IP Library Granted Patent US 10,034,939
Granted Patent B2
US 10,034,939 · App. 14/438,310 · Granted Jul 31, 2018

Synergistic combination of immunologic inhibitors for the treatment of cancer

Inventors: Thomas F. Gajewski (Chicago, IL); Stefani Spranger (Chicago, IL); Michael Leung (Chicago, IL)
Assignee: The University of Chicago
A61K39/39558A61K31/4245A61K45/06A61K2039/507
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Quick Facts
Patent No.
US 10,034,939
App. No.
14/438,310
Granted
Jul 31, 2018
Kind
B2
Abstract

In some embodiments, the methods involve the use of a combination of at least two of the following: an inhibitor of indoleamine-2,3-dioxygenase (IDO), an inhibitor of the PD-L1/PD-1 pathway, an inhibitor of CTLA-4, an inhibitor of CD25, or IL-7. The inventors particularly observed a major synergistic effect of combining anti-CTLA-4 with either an IDO inhibitor, with anti-PD-L1 mAb, or with CD-25 depletion. Such combinations have been found to demonstrate a synergistic effect in treating cancer and tumors, for example by reducing tumor size, increasing the percentage of antigen-specific T cells, and increasing T cell function.

Claims (18)

1. A method of treating melanoma in a subject comprising administering to the subject an effective amount of an inhibitor of the PD-L1 pathway and an inhibitor of indoleamine-2,3-dioxygenase (IDO), wherein the inhibitor of the PD-L1 pathway is BMS-936559, MPDL3280A, BMS-936558, MK-3475, CT-011, or MEDI4736; and wherein the IDO inhibitor is a compound of the formula below

wherein

R 1 is NH 2 or CH 3

R 2 is Cl, F, CF 3 , CH 3 , Br, or CN,

R 3 is H or F,

R 4 is H or CH 3 , and,

n is 1 or 2,

or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein the inhibitor of IDO is the compound:

3. The method of claim 1 , wherein the inhibitor of IDO is the compound:

4. The method of claim 1 , wherein the inhibitor of IDO is the compound:

5. The method of claim 1 , wherein treating melanoma is further defined as reducing the size of a tumor or inhibiting growth of a tumor.

6. The method of claim 1 , wherein the inhibitors are administered to the subject at least two, three, four, five, six, seven, eight, nine or ten times.

7. The method of claim 1 , wherein said subject is further administered a second cancer therapy.

8. The method of claim 7 , wherein said second cancer therapy comprises surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy.

9. The method of claim 1 , wherein the melanoma is a chemotherapy or radio-resistant melanoma.

10. The method of claim 1 , wherein the effective amount comprises at least about 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 150, 200, 250, or 300 μg/kg or mg/kg per subject weight.

11. A method of treating melanoma in a subject comprising administering to the subject an effective amount of an inhibitor of the PD-L1 pathway and an inhibitor of indoleamine-2,3-dioxygenase (IDO), wherein the inhibitor of the PD-L1 pathway is BMS-936559, MPDL3280A, BMS-936558, MK-3475, CT-011, or MEDI4736; and wherein the IDO inhibitor is the compound

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2015
From: GAJEWSKI, THOMAS F.; SPRANGER, STEFANI; LEUNG, MICHAEL
To: THE UNIVERSITY OF CHICAGO
Reel/Frame 035562/0066 →
Continuity (2)
Provisional Application 61719202 · Oct 26, 2012
Related Publication 20150352206A1 · Dec 10, 2015
Cited By (2)
US 12,286,403 US 12,708,667