Claims for Patent: 9,375,434

Summary for Patent: 9,375,434

Title:	Antitumor effect potentiator composed of imidazooxazine compound
Abstract:	An antitumor effect potentiator for potentiating one or more other antitumor agents, comprising, as an active ingredient, an imidazooxazine compound represented by Formula (I), or a pharmaceutically acceptable salt thereof, ##STR00001## wherein A, B, C, and D represent C--R.sup.1a, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) represent(s) halogen; cyano; C.sub.1-6 alkyl that may have hydroxyl group(s) as substituent(s); C.sub.1-6 alkoxy; carbonyl having, as a substituent, hydroxyl, amino, optionally substituted mono- or di-(C.sub.1-6 alkyl)amino, or mono- or di-(C.sub.1-6 alkoxy)amino; or an unsaturated heterocyclic group; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxy.
Inventor(s):	Ichikawa; Koji (Tsukuba, JP), Okada; Megumu (Tsukuba, JP)
Assignee:	Taiho Pharmaceutical Co., Ltd. (Tokyo, JP)
Application Number:	14/407,745
Patent Claims:	1. A method for potentiating one or more antitumor agents, comprising administering an imidazooxazine compound represented by Formula (I), or a pharmaceutically acceptable salt thereof in combination with one or more antitumor agents, wherein said imidazooxazine compound is in an amount effective for potentiating the effect of said one or more antitumor agents, to a patient in need of such treatment, ##STR00196## wherein A, B, C, and D represent C--R.sup.1a, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) represent(s) halogen; cyano; C.sub.1-6 alkyl which is unsubstituted or substituted with a hydroxyl group; C.sub.1-6 alkoxy; carbonyl having, as a substituent, hydroxyl, amino, mono- or di-(C.sub.1-6 alkyl)amino which is substituted with hydroxyl or unsubstituted mono- or di-(C.sub.1-6 alkyl)amino, or mono- or di-(C.sub.1-6 alkoxy)amino; or an unsaturated heterocyclic group; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxy. 2. The method according to claim 1, wherein A, B, C, and D represent C--R.sup.1a, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) individually represent(s) chlorine, fluorine, cyano, methyl, hydroxymethyl, methoxy, ethoxy, carboxyl, carbamoyl, methylaminocarbonyl, ethylaminocarbonyl, hydroxyethylaminocarbonyl, ethoxyaminocarbonyl, or pyrazolyl; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxy. 3. A method for potentiating one or more antitumor agents, comprising administering an imidazooxazine compound of any one of the following (a) to (t), or a salt thereof, as an active ingredient, in combination with one or more antitumor agents, to a patient in need of such treatment, (a) trans-3-amino-1-cyclopropyl-3-(4-(10-fluoro-3-phenyl-5H-benzo[e]imidazo[1- ,2-c][1,3]oxazin-2-yl)phenyl)cyclobutanol, (b) trans-3-amino-1-cyclopropyl-3-(4-(10-fluoro-3-(pyridin-4-yl)-5H-benzo[e]i- midazo[1,2-c][1,3]oxazin-2-yl)phenyl)cyclobutanol, (c) trans-3-amino-1-cyclopropyl-3-(4-(3-phenyl-5H-benzo[e]imidazo[1,2-c][1,3]- oxazin-2-yl)phenyl)cyclobutanol, (d) trans-3-amino-1-cyclopropyl-3-(4-(10-methoxy-3-phenyl-5H-benzo[e]imidazo[- 1,2-c][1,3]oxazin-2-yl)phenyl)cyclobutanol, (e) trans-3-amino-1-cyclopropyl-3-(4-(9-methoxy-3-phenyl-5H-benzo[e]imidazo[1- ,2-c][1,3]oxazin-2-yl)phenyl)cyclobutanol, (f) trans-3-amino-1-cyclopropyl-3-(4-(8-methoxy-3-phenyl-5H-benzo[e]imidazo[1- ,2-c][1,3]oxazin-2-yl)phenyl)cyclobutanol, (g) trans-3-amino-1-cyclopropyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[2,3-e]- [1,3]oxazin-2-yl)phenyl)cyclobutanol, (h) trans-3-amino-1-methyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[2,3-e][1,3]- oxazin-2-yl)phenyl)cyclobutanol, (i) trans-3-amino-1-ethyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[2,3-e][1,3]o- xazin-2-yl)phenyl)cyclobutanol, (j) trans-3-amino-1-cyclopropyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[3,4-e]- [1,3]oxazin-2-yl)phenyl)cyclobutanol, (k) trans-3-amino-1-methyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[3,4-e][1,3]- oxazin-2-yl)phenyl)cyclobutanol, (l) trans-3-amino-1-cyclopropyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[4,3-e]- [1,3]oxazin-2-yl)phenyl)cyclobutanol, (m) trans-3-amino-1-methyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[4,3-e][1,3]- oxazin-2-yl)phenyl)cyclobutanol, (n) trans-3-amino-1-cyclopropyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrido[3,2-e]- [1,3]oxazin-2-yl)phenyl)cyclobutanol, (o) trans-3-amino-1-cyclopropyl-3-(4-(3-phenyl-5H-imidazo[1,2-c]pyrazino[2,3-- e][1,3]oxazin-2-yl)phenyl)cyclobutanol, (p) trans-3-amino-3-(4-(9-(hydroxymethyl)-3-phenyl-5H-benzo[e]imidazo[1,2-c][- 1,3]oxazin-2-yl)phenyl)-1-methylcyclobutanol, (q) 2-(4-(trans-1-amino-3-hydroxy-3-methylcyclobutyl)phenyl)-3-phenyl-5H-benz- o[e]imidazo[1,2-c][1,3]oxazine-9-carbonitrile, (r) trans-3-amino-1-methyl-3-(4-(3-phenyl-9-(1H-pyrazol-5-yl)-5H-benzo[e]imid- azo[1,2-c][1,3]oxazin-2-yl)phenyl)cyclobutanol, (s) 2-(4-(trans-1-amino-3-hydroxy-3-methylcyclobutyl)phenyl)-N-methyl-3-pheny- l-5H-benzo[e]imidazo[1,2-c][1,3]oxazine-8-carboxamide, and (t) 2-(4-(trans-1-amino-3-hydroxy-3-methylcyclobutyl)phenyl)-N-ethoxy-3-pheny- l-5H-benzo[e]imidazo[1,2-c][1,3]oxazine-8-carboxamide. 4. An antitumor composition comprising an imidazooxazine compound or a pharmaceutically acceptable salt thereof in combination with one or more antitumor agents, wherein said imidazooxazine compound is represented by Formula (I), or a pharmaceutically acceptable salt thereof, in an amount effective for potentiating the effect of said one or more antitumor agents, ##STR00197## wherein A, B, C, and D represent C--R.sup.1a, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) re resent s halogen; cyano; C.sub.1-6 allyl; C.sub.1-6 alkoxy; carbonyl having, as a substituent, hydroxyl; amino, mono- or di-(C.sub.1-6 alkyl)amino substituted with hydroxyl or unsubstituted mono- or di-(C.sub.1-6 alkyl)amino or mono- or di-(C.sub.1-6 alkoxy)amino; or an unsaturated heterocyclic group; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxy. 5. A method for making an antitumor composition, comprising combining an imidazooxazine compound or a pharmaceutically acceptable salt thereof with one or more antitumor agents and a pharmaceutically acceptable carrier, wherein said imidazooxazine compound is represented by Formula (I), or a pharmaceutically acceptable salt thereof, in an amount effective for potentiating the effect of said one or more antitumor agents, ##STR00198## wherein A, B, C, and D represent C--R.sup.1, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) re resent s halogen; cyano; C.sub.1-6 alkyl; C.sub.1-6 alkoxy; carbonyl having, as a substituent, hydroxyl, amino, mono- or di-(C.sub.1-6 alkyl)amino substituted with hydroxyl or unsubstituted mono- or di-(C.sub.1-6 alkyl)amino or mono- or di-(C.sub.1-6 alkoxy)amino; or an unsaturated heterocyclic group; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxy. 6. The method according to claim 1, wherein the one or more antitumor agents are selected from the group consisting of paclitaxel, carboplatin, lapatinib, irinotecan, doxorubicin, everolimus, bortezomib, erlotinib, trastuzumab (herceptin), metformin, docetaxel, and a combination drug of tegafur, gimeracil, and oteracil potassium. 7. A pharmaceutical composition comprising an imidazooxazine compound or a pharmaceutically acceptable salt thereof, a pharmaceutically acceptable carrier and one or more antitumor agents, wherein said imidazooxazine compound is represented by Formula (I), or a pharmaceutically acceptable salt thereof, in an amount effective for potentiating the effect of said one or more antitumor agents, ##STR00199## wherein A, B, C, and D represent C--R.sup.1a, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) re resent s halogen; cyano; C.sub.1-6 alkyl; C.sub.1-6 alkoxy; carbonyl having, as a substituent, hydroxyl, amino, mono- or di-(C.sub.1-6 alkyl)amino substituted with hydroxyl or unsubstituted mono- or di-(C.sub.1-6 alkyl)amino or mono- or di-(C.sub.1-6 alkoxy)amino; or an unsaturated heterocyclic group; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxy. 8. A method for treating a malignant tumor in which AKT (serine/threonine-specific kinase) is frequently activated or highly expressed, comprising administering to a patient a combination of a imidazooxazine compound or a pharmaceutically acceptable salt thereof and one or more antitumor agents in an amount effective for treatment of said malignant tumor, wherein said imidazooxazine compound is represented by Formula (I), or a pharmaceutically acceptable salt thereof, in an amount effective for potentiating the effect of said one or more antitumor agents, ##STR00200## wherein A, B, C, and D represent C--R.sup.1a, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) re resent s halogen; cyano; C.sub.1-6 alkyl; C.sub.1-6 alkoxy; carbonyl having, as a substituent, hydroxyl, amino, mono- or di-(C.sub.1-6 alkyl)amino substituted with hydroxyl or unsubstituted mono- or di-(C.sub.1-6 alkyl)amino or mono- or di-(C.sub.1-6 alkoxy)amino; or an unsaturated heterocyclic group; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxy. 9. A kit for the treatment of malignant tumors, comprising an imidazooxazine compound or a pharmaceutically acceptable salt thereof and one or more antitumor agents wherein said imidazooxazine compound is represented by Formula (I), or a pharmaceutically acceptable salt thereof, in an amount effective for potentiating the effect of said one or more antitumor agents, ##STR00201## wherein A, B, C, and D represent C--R.sup.1a, C--R.sup.1b, C--R.sup.1c, and C--R.sup.1d, respectively, or one or two of A, B, C, and D represent an N atom; at least two of R.sup.1a, R.sup.1b, R.sup.1c, and R.sup.1d represent hydrogen, and the other(s) represent(s) halogen; cyano; C.sub.1-6 alkyl; C.sub.1-6 alkoxy; carbonyl having, as a substituent, hydroxyl, amino, mono- or di-(C.sub.1-6 alkyl)amino substituted with hydroxyl or unsubstituted mono- or di-(C.sub.1-6 alkyl)amino or mono- or di-(C.sub.1-6 alkoxy)amino; or an unsaturated heterocyclic group; R.sup.2 represents phenyl, pyridyl, or thienyl; R.sup.3 represents hydrogen, methyl, ethyl, or cyclopropyl; and R.sup.4 represents hydrogen or hydroxyl. 10. The antitumor composition according to claim 4, wherein the one or more antitumor agents are selected from the group consisting of paclitaxel, carboplatin, lapatinib, irinotecan, doxorubicin, everolimus, bortezomib, erlotinib, trastuzumab (herceptin), metformin, docetaxel, and a combination drug of tegafur, gimeracil, and oteracil potassium. 11. The method according to claim 1, wherein said C.sub.1-6 alkyl has hydroxyl group(s) as substituent(s). 12. The method according to claim 8, wherein said malignant tumor in which AKT serine/threonine-specific kinase is frequently activated or highly expressed is a cancer selected from the group consisting of head and neck cancer, esophagus cancer, stomach cancer, colon cancer, rectum cancer, hepatocarcinoma, gallbladder cancer, cholangiocarcinoma, pancreatic cancer, lung cancer, breast cancer, ovarian cancer, cervical cancer, endometrial cancer, renal cancer, bladder cancer, prostate cancer, testicular tumor, osteosarcoma, soft-tissue sarcoma, leukemia, malignant lymphoma, multiple myeloma, skin cancer, and a brain tumor.

Details for Patent 9,375,434

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	09/25/1998		2032-07-02
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	02/10/2017		2032-07-02
Genentech, Inc.	HERCEPTIN HYLECTA	trastuzumab and hyaluronidase-oysk	Injection	761106	02/28/2019		2032-07-02