Claims for Patent: 9,717,717

Summary for Patent: 9,717,717

Title:	Methods of treating cancer through the inhibition of USP7 and immune system modulation
Abstract:	Methods and compounds for treating cancer by, for example, modulating immune system activity, are provided.
Inventor(s):	Weinstock; Joseph (Wayne, PA), Wu; Jian (Chester Springs, PA), Kizhakkethil-George; Suresh Kumar (Downingtown, PA), Wang; Feng (Devon, PA), Kodrasov; Matthew P. (Cherry Hill, NJ), Agarwal; Saket (Woburn, MA), Hancock; Wayne W. (Philadelphia, PA)
Assignee:	Progenra, Inc. (Malvern, PA) The Children\'s Hospital of Philadelphia (Philadelphia, PA)
Application Number:	15/222,204
Patent Claims:	1. A method for treating cancer in a patient in need thereof by modulating immune system activity, said method comprising administering to said patient an amount of a USP7 inhibitor that is effective to reduce Treg cell activity and increase Teff cell activity, the USP7 inhibitor being at least one compound of formula II: ##STR00006## wherein X is nitro or cyano; R.sub.5 is H or optionally substituted alkyl; R.sub.6 is selected from the group consisting of H, halo, hydroxyl, and optionally substituted alkyl, aryl, alkoxy, aryloxy, heteroaryl, cycloalkyl, heteroarylalkyl, sulfonyl, sulfamide, sulfonamide, --C(O)OH, --C(O)OR.sub.7, carboxamido, amino, monoalkylamino, dialkylamino, dialkylaminoalkylamino, thionyl, sulfoxy, alkyl-S(O).sub.n, and cycloalkyl-S(O)n, aryl-S(O).sub.n; R.sub.7 is H or alkyl; n is 0-2; and the pharmaceutically acceptable salts thereof, wherein the cancer is lung cancer. 2. The method of claim 1, wherein R.sub.6 is a substituent selected from the group consisting of halo, methoxy, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, cyclopropylsulfonyl, cyclobutylsulfonyl, cyclopentylsulfonyl, cyclohexylsulfonyl, methylthionyl, methylsulfoxyl, methylsulfonylmethyl, N-methylsulfonamido, trifluoromethylsulfonyl, 2-hydroxyethylsulfonyl, cyclopropylsulfonamido, cyclopropylmethylsulfonyl, methylsulfonamido, 2-(Me.sub.2N)-ethoxy, 2-(Me.sub.2N)-ethylamino, and pyridinyl. 3. The method of claim 1, comprising administering the amount of the USP7 inhibitor together with a pharmaceutically acceptable excipient, carrier, diluents, or a combination thereof. 4. The method of claim 1, further comprising administering to said patient an anticancer vaccine, an anticancer immunotherapy agent, anti-cancer immunomodulatory agent, an additional anticancer therapeutic, radiation therapy or a combination thereof. 5. The method of claim 4, wherein the anticancer vaccine is selected from the group consisting of Gardasil, Cervarix, and Sipuleucel-T/Provenge. 6. The method of claim 4, wherein the anticancer immunotherapy agent is selected from the group consisting of Alemtuzumab, Ipilimumab, Nivolumab, Pembrolizumab, Rituximab, Interferon, Interleukin, and a combination thereof. 7. The method of claim 4, wherein the anti-cancer immunomodulatory agent is selected from the group consisting of thalidomide, lenolidomide, pomalidomide, and a combination thereof. 8. The method of claim 4, wherein the additional anticancer therapeutic is selected from the group consisting of an alkylating agent, a tubulin inhibitor, a topoisomerase inhibitor, proteasome inhibitor, a CHK1 inhibitor, a CHK2 inhibitor, PARP inhibitor, doxorubicin, epirubicin, vinblastine, etoposide, topotecan, bleomycin, and mytomycin c. 9. The method of claim 8, wherein said alkylating agent is selected from the group consisting of Dacarbazine, Procarbazine, Carmustine, Lomustine, Uramustine, Busulfan, Streptozocin, Altreamine, Ifosfamine, Chrormethine, Cyclophasphamide, Cyclophosphamide, Chlorambucil, Fluorouracil (5-Fu), Melphalan, Triplatin tetranitrate, Satraplatin, Nedaplatin, Cisplatin, Carboplatin, and Oxaliplatin. 10. The method of claim 8, wherein said tubulin inhibitor is selected from the group consisting of Taxol, Docetaxel, Vinblastin, Epothilone, Colchicine, Cryptophycin, BMS-347550, Rhizoxin, Ecteinascidin, Dolastin 10, Cryptophycin 52, and IDN-5109. 11. The method of claim 8, wherein said topoisomerase inhibitor is a topoisomerase I inhibitor selected from the group consisting of Irinotecan, Topotecan, and Camptothecins (CPT). 12. The method of claim 8, wherein said topoisomerase inhibitor is a topoisomerase II inhibitor selected from the group consisting of Amsacrine, Etoposide, Teniposide, Epipodophyllotoxins, and ellipticine. 13. The method of claim 8, wherein said proteasome inhibitor is selected from the group consisting of Velcade (bortezomib), and Kyprolis (carfilzomib). 14. The method of claim 8, wherein said CHK1 inhibitor is selected from the group consisting of TCS2312, PF-0047736, AZ07762, A-69002, and A-641397. 15. The method of claim 8, wherein the PARP inhibitor is selected from the group consisting of Olaparib, ABT-888, (veliparib), KU-59436, AZD-2281, AG-014699, BSI-201, BGP-15, INO-1001, ONO-2231 and the like. 16. The method of claim 8, wherein radiation therapy is administered to said patient. 17. The method of claim 1, wherein the at least one compound comprises an irreversible inhibitor of USP7. 18. The method of claim 1, wherein X in said formula represents nitro.

Details for Patent 9,717,717

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	RITUXAN	rituximab	Injection	103705	11/26/1997		2035-07-31
Idec Pharmaceuticals Corp.	RITUXAN	rituximab	Injection	103737	02/19/2002		2035-07-31
Genzyme Corporation	CAMPATH	alemtuzumab	Injection	103948	05/07/2001		2035-07-31