Combination therapy for the treatment or prevention of tumours
The present invention relates to a combination therapy for tumours comprising the administration of an epoxytigliane compound and an immune checkpoint inhibitor. In particular embodiments, there is a method of treating a tumour and/or treating or preventing one or more bystander tumours with the therapy. Pharmaceutical compositions and kits containing epoxytigliane compounds and immune checkpoint inhibitors are also described.
1. A method of treating a tumour comprising administering to a subject in need thereof, an epoxytigliane compound or a pharmaceutically acceptable salt thereof and an immune checkpoint inhibitor; wherein the epoxytigliane compound is administered locally to the tumour;
wherein the epoxytigliane compound is a compound of formula (I):
or a geometric isomer or stereoisomer or a pharmaceutically acceptable salt thereof;
wherein
R 1 is hydrogen or C 1-6 alkyl;
R 2 is —OH or —OR 9 ;
R 3 is —OH or —OR 9 ;
R 4 and R 5 are independently selected from hydrogen and C 1-6 alkyl;
R 6 is hydrogen or —R 10 ;
R 7 is hydroxy or OR 10 ;
R 8 is hydrogen or C 1-6 alkyl;
R 9 is —C 1-20 alkyl, —C 2-20 alkenyl, —C 2-20 alkynyl, —C(O)C 1-20 alkyl, —C(O)C 2-20 alkenyl, —C(O)C 2-20 alkynyl, —C(O)cycloalkyl, —C(O)C 1-10 alkyl-cycloalkyl; —C(O)C 2-10 alkenylcycloalkyl, —C(O)C 2-10 alkynylcycloalkyl, —C(O)aryl, —C(O)C 1-10 alkylaryl, —C(O)C 2-10 alkenylaryl, —C(O)C 2-10 alkynylaryl, —C(O)C 1-10 alkylC(O)R 11 , —C(O)C 2-10 alkenylC(O)R 11 , —C(O)C 2-10 alkynylC(O)R 11 , —C(O)C 1-10 alkylCH(OR 11 )(OR 11 ), —C(O)C 2-10 alkenyl-CH(OR 11 )(OR 11 ), —C(O)C 2-10 alkynylCH(OR 11 )(OR 11 ), —C(O)C 1-10 alkylSR 11 , —C(O)C 2-10 alkenylSR 11 , —C(O)C 2-10 alkynylSR 11 , —C(O)C 1-10 alkylC(O)OR 11 , —C(O)C 2-10 alkenylC(O)OR 11 , —C(O)C 2-10 alkynylC(O)OR 11 , —C(O)C 1-10 alkyl-C(O)SR 11 , —C(O)C 2-10 alkenylC(O)SR 11 , —C(O)C 2-10 alkynylC(O)SR 11 ,
R 10 is —C 1-6 alkyl, —C 2-6 alkenyl, —C 2-6 alkynyl, —C(O)C 1-6 alkyl, —C(O)C 2-6 alkenyl, —C(O)C 2-6 alkynyl, —C(O)aryl, —C(O)C 1-6 alkylaryl, —C(O)C 2-6 alkenylaryl, or —C(O)C 2-6 alkynylaryl; and
R 11 is hydrogen, —C 1-10 alkyl, —C 2-10 alkenyl, —C 2-10 alkynyl, cycloalkyl or aryl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl or aryl group is optionally substituted with one or more optional substituents selected from the group consisting of C 1-6 alkyl, C 2-6 alkenyl, C 3-6 cycloalkyl, oxo (═O), —OH, —SH, C 1-6 alkylO-, C 2-6 alkenylO-, C 3-6 cycloalkylO-, C 1-6 alkylS-, C 2-6 alkenylS-, C 3-6 cycloalkylS-, —CO 2 H, —CO 2 C 1-6 alkyl, —NH 2 , —NH(C 1-6 alkyl), —N(C 1-6 alkyl) 2 , —NH(phenyl), —N(phenyl) 2 , —CN, —NO 2 , -halogen, —CF 3 , —OCF 3 , —SCF 3 , —CHF 2 , —OCHF 2 , —SCHF 2 , -phenyl, —C 1-6 alkylphenyl, —Ophenyl, —C(O)phenyl, and —C(O)C 1-6 alkyl;
wherein the immune checkpoint inhibitor is selected from an antagonist of Programmed Death 1 (PD-1) receptor or its ligand PD-L1, and an antagonist of Cytotoxic T-Lymphocyte-Associated protein 4 (CTLA-4); and
wherein the tumour is one that has acquired or has intrinsic resistance to monotherapy with the immune checkpoint inhibitor.
2. A method of treating one or more bystander tumours in a subject comprising administering to a subject in need thereof, an epoxytigliane compound or a pharmaceutically acceptable salt thereof and an immune checkpoint inhibitor; wherein the epoxytigliane compound is administered locally to a tumour other than the one or more bystander tumours;
wherein the epoxytigliane compound is a compound of formula (I):
or a geometric isomer or stereoisomer or a pharmaceutically acceptable salt thereof;
wherein
R 1 is hydrogen or C 1-6 alkyl;
R 2 is —OH or —OR 9 ;
R 3 is —OH or —OR 9 ;
R 4 and R 5 are independently selected from hydrogen and C 1-6 alkyl;
R 6 is hydrogen or —R 10 ;
R 7 is hydroxy or OR 10 ;
R 5 is hydrogen or C 1-6 alkyl;
R 9 is —C 1-20 alkyl, —C 2-20 alkenyl, —C 2-20 alkynyl, —C(O)C 1-20 alkyl, —C(O)C 2-20 alkenyl, —C(O)C 2-20 alkynyl, —C(O)cycloalkyl, —C(O)C 1-10 alkyl-cycloalkyl; —C(O)C 2-10 alkenylcycloalkyl, —C(O)C 2-10 alkynylcycloalkyl, —C(O)aryl, —C(O)C 1-10 alkylaryl, —C(O)C 2-10 alkenylaryl, —C(O)C 2-10 alkynylaryl, —C(O)C 1-10 alkylC(O)R 11 , —C(O)C 2-10 alkenylC(O)R 11 , —C(O)C 2-10 alkynylC(O)R 11 , —C(O)C 1-10 alkylCH(OR 11 )(OR 11 ), —C(O)C 2-10 alkenyl-CH(OR 11 )(OR 11 ), —C(O)C 2-10 alkynylCH(OR 11 )(OR 11 ), —C(O)C 1-10 alkylSR 11 , —C(O)C 2-10 alkenylSR 11 , —C(O)C 2-10 alkynylSR 11 , —C(O)C 1-10 alkylC(O)OR 11 , —C(O)C 2-10 alkenylC(O)OR 11 , —C(O)C 2-10 alkynylC(O)OR 11 , —C(O)C 1-10 alkyl-C(O)SR 11 , —C(O)C 2-10 alkenylC(O)SR 11 , —C(O)C 2-10 alkynylC(O)SR 11 ,
R 10 is —C 1-6 alkyl, —C 2-6 alkenyl, —C 2-6 alkynyl, —C(O)C 1-6 alkyl, —C(O)C 2-6 alkenyl, —C(O)C 2-6 alkynyl, —C(O)aryl, —C(O)C 1-6 alkylaryl, —C(O)C 2-6 alkenylaryl, or —C(O)C 2-6 alkynylaryl; and
R 11 is hydrogen, —C 1-10 alkyl, —C 2-10 alkenyl, —C 2-10 alkynyl, cycloalkyl or aryl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl or aryl group is optionally substituted with one or more optional substituents selected from the group consisting of C 1-6 alkyl, C 2-6 alkenyl, C 3-6 cycloalkyl, oxo (═O), —OH, —SH, C 1-6 alkylO-, C 2-6 alkenylO-, C 3-6 cycloalkylO-, C 1-6 alkylS-, C 2-6 alkenylS-, C 3-6 cycloalkylS-, —CO 2 H, —CO 2 C 1-6 alkyl, —NH 2 , —NH(C 1-6 alkyl), —N(C 1-6 alkyl) 2 , —NH(phenyl), —N(phenyl) 2 , —CN, —NO 2 , -halogen, —CF 3 , —OCF 3 , —SCF 3 , —CHF 2 , —OCHF 2 , —SCHF 2 , -phenyl, —C 1-6 alkylphenyl, —Ophenyl, —C(O)phenyl, and —C(O)C 1-6 alkyl;
wherein the immune checkpoint inhibitor is selected from an antagonist of Programmed Death 1 (PD-1) receptor or its ligand PD-L1, or an antagonist of Cytotoxic T-Lymphocyte-Associated protein 4 (CTLA-4), and
wherein the tumour to which the epoxytigliane is administered is one that has acquired or has intrinsic resistance to monotherapy with the immune checkpoint inhibitor.
3. The method according to claim 1 wherein the epoxytigliane compound is administered by intra-tumoural injection.
4. The method according to claim 1 wherein the immune checkpoint inhibitor is administered systemically.
5. The method according to claim 4 wherein the immune checkpoint inhibitor is administered by parenteral injection.
6. The method according to claim 1 wherein R 1 is —CH 3 .
7. The method according to claim 1 wherein R 2 and R 3 are independently selected from —OC(O)C 1-20 alkyl, —OC(O)C 2-20 alkenyl, —OC(O)C 2-20 alkynyl, —OC(O)cycloalkyl, —OC(O)C 1-10 alkylcycloalkyl; —OC(O)C 2-10 alkenylcycloalkyl, —OC(O)C 2-10 alkynylcycloalkyl, —OC(O)aryl, —OC(O)C 1-10 alkylaryl, —OC(O)C 2-10 alkenylaryl, —OC(O)C 2-10 alkynylaryl, —OC(O)C 1-10 alkylC(O)R 11 , —OC(O)C 2-10 alkenylC(O)R 11 , —OC(O)C 2-10 alkynylC(O)R 11 , —OC(O)C 1-10 alkylCH(OR 11 )(OR 11 ), —OC(O)C 2-10 alkenylCH(OR 11 )(OR 11 ), —OC(O)C 2-10 alkynylCH(OR 11 )(OR 11 ), —OC(O)C 1-10 alkylSR 11 , —OC(O)C 2-10 alkenylSR 11 , —OC(O)C 2-10 alkynylSR 11 , —OC(O)C 1-10 alkylC(O)OR 11 , —OC(O)C 2-10 alkenylC(O)OR 11 , —OC(O)C 2-10 alkynylC(O)OR 11 , —OC(O)C 1-10 alkylC(O)SR 11 , —OC(O)C 2-10 alkenylC(O)SR 11 and —OC(O)C 2-10 alkynylC(O)SR 11 .
8. The method according to claim 1 wherein R 4 and R 5 are each independently selected from H and —CH 3 .
9. The method according to claim 1 wherein R 6 is hydrogen, —C(O)C 1-6 alkyl, —C(O)C 2-6 alkenyl, —C(O)C 2-6 alkynyl or —C(O)aryl.
10. The method according to claim 1 wherein R 7 is hydroxyl, —OC(O)C 1-6 alkyl, —OC(O)C 2-6 alkenyl or —OC(O)C 2-6 alkynyl.
11. The method according to claim 1 wherein R 5 is H or —CH 3 .
12. The method according to claim 1 wherein the epoxytigliane compound of formula (I) is selected from the following compounds:
12-tigloyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12,13-di-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-hexanoyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12,13-dihexanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-myristoyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-tigloyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13-pentahydroxy-20-acetyloxy-1-tiglien-3-one;
12-myristoyl-13-acetyloxy-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-propanoyl-13-2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one; 12,13-ditigloyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one; and
12-(2-methylbutanoyl)-13-tigloyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
or a pharmaceutically acceptable salt thereof.
13. The method according to claim 1 wherein the immune checkpoint inhibitor is an antagonist of Programmed Death 1 (PD-1) receptor or Cytotoxic T-Lymphocyte-Associated protein 4 (CTLA-4).
14. The method according to claim 1 wherein the immune checkpoint inhibitor is administered in multiple doses.
15. The method according to claim 14 wherein the multiple doses are administered prior to, simultaneously with and/or subsequent to the administration of the epoxytigliane compound.
16. A pharmaceutical composition comprising an epoxytigliane compound or a pharmaceutically acceptable salt thereof and an immune checkpoint inhibitor and optionally a pharmaceutically acceptable carrier; wherein the epoxytigliane compound is a compound of formula (I):
or a geometric isomer or stereoisomer or a pharmaceutically acceptable salt thereof,
wherein
R 1 is hydrogen or C 1-6 alkyl,
R 2 is —OH or —OR 9 ;
R 3 is —OH or —OR 9 ;
R 4 and R 5 are independently selected from hydrogen and C 1-6 alkyl,
R 6 is hydrogen or -R 10 ;
R 7 is hydroxy or OR 10 ;
R 8 is hydrogen or C 1-6 alkyl;
R 9 is —C 1-20 alkyl, —C 2-20 alkenyl, —C 2-20 alkynyl, —C(O)C 1-20 alkyl, —C(O)C 2-20 alkenyl, —C(O)C 2-20 alkynyl, —C(O)cycloalkyl, —C(O)C 1-10 alkyl-cycloalkyl, —C(O)C 2-10 alkenylcycloalkyl, —C(O)C 2-10 alkynylcycloalkyl, —C(O)aryl, —C(O)C 1-10 alkylaryl, —C(O)C 2-10 alkenylaryl, —C(O)C 2-10 alkynylaryl, —C(O)C 1-10 alkylC(O)R 11 , —C(O)C 2-10 alkenylC(O)R 11 , —C(O)C 2-10 alkynylC(O)R 11 , —C(O)C 1-10 alkylCH(OR 11 )(OR 11 ), —C(O)C 2-10 alkenylCH(OR 11 )(OR 11 ), —C(O)C 2-10 alkynylCH(OR 11 )(OR 11 ), —C(O)C 1-10 alkylSR 11 , —C(O)C 2-10 alkenylSR 11 , —C(O)C 2-10 alkynylSR 11 , —C(O)C 1-10 alkylC(O)OR 11 , —C(O)C 2-10 alkenylC(O)OR 11 , —C(O)C 2-10 alkynylC(O)OR 11 , —C(O)C 1-10 alkyl-C(O)SR 11 , —C(O)C 2-10 alkenylC(O)SR 11 , —C(O)C 2-10 alkynylC(O) SR 11 ,
R 10 is —C 1-6 alkyl, —C 2-6 alkenyl, —C 2-6 alkynyl, —C(O)C 1-6 alkyl, —C(O)C 2-6 alkenyl, —C(O)C 2-6 alkynyl, —C(O)aryl, —C(O)C 1-6 alkylaryl, —C(O)C 2-6 alkenylaryl, or —C(O)C 2-6 alkynylaryl, and
R 11 is hydrogen, —C 1-10 alkyl, cycloalkyl or aryl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl or aryl group is optionally substituted with one or more optional substituents selected from the group consisting of C 1-6 alkyl, C 2-6 alkenyl, C 3-6 cycloalkyl, oxo (═O), —OH, —SH, C 1-6 alkylO-, C 2-6 alkenylO-, C 3-6 cycloalkylO-, C 1-6 alkylS-, C 2-6 alkenylS-, C 3-6 cycloalkylS-, —CO 2 H, —CO 2 C 1-6 alkyl, —NH 2 , —NH(C 1-6 alkyl), —N(C 1-6 alkyl) 2 , —NH(phenyl), —N(phenyl) 2 , —CN, —NO 2 , -halogen, —CF 3 , —OCF 3 , —SCF 3 , —CHF 2 , —OCHF 2 , —SCHF 2 —, -phenyl, —C 1-6 alkylphenyl, —Ophenyl, —C(O)phenyl, and —C(O)C 1-6 alkyl; and
wherein the immune checkpoint inhibitor is selected from an antagonist of Programmed Death 1 (PD-1) receptor or its ligand PD-L1, or an antagonist of Cytotoxic T-Lymphocyte-Associated protein 4 (CTLA-4).
17. The kit comprising one or more doses of epoxytigliane compound and one or more doses of immune checkpoint inhibitor; wherein the epoxytigliane compound is a compound of formula (I):
or a geometric isomer or stereoisomer or a pharmaceutically acceptable salt thereof;
wherein
R 1 is hydrogen or C 1-6 alkyl;
R 2 is —OH or —OR 9 ;
R 3 is —OH or —OR 9 ;
R 4 and R 5 are independently selected from hydrogen and C 1-6 alkyl;
R 6 is hydrogen or -R 10 ;
R 7 is hydroxy or OR 10 ;
R 5 is hydrogen or C 1-6 alkyl;
R 9 is —C 1-20 alkyl, —C 2-20 alkenyl, —C 2-20 alkynyl, —C(O)C 1-20 alkyl, —C(O)C 2-20 alkenyl, —C(O)C 2-20 alkynyl, —C(O)cycloalkyl, —C(O)C 1-10 alkylcycloalkyl; —C(O)C 2-10 alkenyl-cycloalkyl, —C(O)C 2-10 alkynylcycloalkyl, —C(O)aryl, —C(O)C 1-10 alkylaryl, —C(O)C 2-10 alkenylaryl, —C(O)C 2-10 alkynylaryl, —C(O)C 1-10 alkylC(O)R 11 , —C(O)C 2-10 alkenylC(O)R 11 , —C(O)C 2-10 alkynylC(O)R 11 , —C(O)C 1-10 alkylCH(OR 11 )(OR 11 ), —C(O)C 2-10 alkenylCH(OR 11 )(OR 11 ), —C(O)C 2-10 alkynylCH(OR 11 )(OR 11 ), —C(O)C 1-10 alkylSR 11 , —C(O)C 2-10 alkenylSR 11 , —C(O)C 2-10 alkynylSR 11 , —C(O)C 1-10 alkylC(O)OR 11 , —C(O)C 2-10 alkenylC(O)OR 11 , —C(O)C 2-10 alkynylC(O)OR 11 , —C(O)C 1-10 alkyl-C(O) SR 11 , —C(O)C 2-10 alkenylC(O) SR 11 , —C(O)C 2-10 alkynylC(O)SR 11 ,
R 10 is —C 1-6 alkyl, —C 2-6 alkenyl, —C 2-6 alkynyl, —C(O)C 1-6 alkyl, —C(O)C 2-6 alkenyl, —C(O)C 2-6 alkynyl, —C(O)aryl, —C(O)C 1-6 alkylaryl, —C(O)C 2-6 alkenylaryl, or —C(O)C 2-6 alkynylaryl; and
R 11 is hydrogen, —C 1-10 alkyl, —C 2-10 alkenyl, —C 2-10 alkynyl, cycloalkyl or aryl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl or aryl group is optionally substituted with one or more optional substituents selected from the group consisting of C 1-6 alkyl, C 2-6 alkenyl, C 3-6 cycloalkyl, oxo (═O), —OH, —SH, C 1-6 alkylO-, C 2-6 alkenylO-, C 3-6 cycloalkylO-, C 1-6 alkylS-, C 2-6 alkenylS-, C 3-6 cycloalkylS-, —CO 2 H, —CO 2 C 1-6 alkyl, —NH 2 , —NH(C 1-6 alkyl), —N(C 1-6 alkyl), —NH(phenyl), —N(phenyl) 2 , —CN, —NO, -halogen, —CF, —OCHF 2 , —SCHF 2 , -phenyl, —C 1-6 alkylphenyl, —Ophenyl, —C(O)phenyl, and —C(O)C 1-6 alkyl; and
wherein the immune checkpoint inhibitor is selected from an antagonist of Programmed Death 1 (PD-1) receptor or its ligand PD-L1, or an antagonist of Cytotoxic T-Lymphocyte-Associated protein 4 (CTLA-4).
18. The kit according to claim 17 comprising one or more doses of epoxytigliane compound formulated for topical administration and one or more doses of immune checkpoint inhibitor formulated for administration by injection.
19. The kit according to claim 17 comprising one dose of epoxytigliane compound formulated for intra-tumoural injection and one or more doses of immune checkpoint inhibitor formulated for administration by injection.
20. The method according to claim 2 wherein the epoxytigliane compound is administered by intra-tumoural injection.
21. The method according to claim 2 wherein the immune checkpoint inhibitor is administered systemically.
22. The method according to claim 21 wherein the immune checkpoint inhibitor is administered by parenteral injection.
23. The method according to claim 2 wherein one or more of the following applies:
i) R 1 is —CH 3 ;
ii) R 2 and R 3 are independently selected from —OC(O)C 1-20 alkyl, —OC(O)C 2-20 alkenyl, —OC(O)C 2-20 alkynyl, —OC(O)cycloalkyl, —OC(O)C 1-10 alkylcycloalkyl; —OC(O)C 2-10 alkenylcycloalkyl, —OC(O)C 2-10 alkynylcycloalkyl, —OC(O)aryl, —OC(O)C 1-10 alkylaryl, —OC(O)C 2-10 alkenylaryl, —OC(O)C 2-10 alkynylaryl, —OC(O)C 1-10 alkylC(O)R 11 , —OC(O)C 2-10 alkenylC(O)R 11 , —OC(O)C 2-10 alkynylC(O)R 11 , —OC(O)C 1-10 alkylCH(OR 11 )(OR 11 ), —OC(O)C 2-10 alkenylCH(OR 11 ) (OR 11 ), —OC(O)C 2-10 alkynylCH(OR 11 )(OR 11 ), —OC(O)C 1-10 alkylSR 11 , —OC(O)C 2-10 alkenylSR 11 , —OC(O)C 2-10 alkynylSR 11 , —OC(O)C 1-10 alkylC(O)OR 11 , —OC(O)C 2-10 alkenylC(O)OR 11 , —OC(O) C 2-10 alkynylC(O)OR 11 , —OC(O)C 1-10 alkylC(O)SR 11 , —OC(O)C 2-10 alkenylC(O)SR 11 and —OC(O)C 2-10 alkynylC(O)SR 11 ;
iii) R 4 and R 5 are each independently selected from H and —CH 3 ;
iv) R 6 is hydrogen, —C(O)C 1-6 alkyl, —C(O)C 2-6 alkenyl, —C(O)C 2-6 alkynyl or —C(O)aryl;
v) R 7 is hydroxyl, —OC(O)C 1-6 alkyl, —OC(O)C 2-6 alkenyl or —OC(O)C 2-6 alkynyl; and
vi) R 5 is H or —CH 3 .
24. The method according to claim 2 wherein the epoxytigliane compound of formula (I) is selected from the following compounds:
12-tigloyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12,13-di-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-hexanoyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12,13-dihexanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-myristoyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-tigloyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13-pentahydroxy-20-acetyloxy-1-tiglien-3-one;
12-myristoyl-13-acetyloxy-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
12-propanoyl-13-2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one; 12,13-ditigloyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one; and
12-(2-methylbutanoyl)-13-tigloyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tiglien-3-one;
or a pharmaceutically acceptable salt thereof.
25. The method according to claim 2 wherein the immune checkpoint inhibitor is an antagonist of Programmed Death 1 (PD-1) receptor or Cytotoxic T-Lymphocyte-Associated protein 4 (CTLA-4).
26. The method according to claim 25 wherein the immune checkpoint inhibitor is selected from an anti-PD-1 antibody and an anti-CTLA4 antibody.
27. The method according to claim 2 wherein the immune checkpoint inhibitor is administered in multiple doses.
28. The method according to claim 27 wherein the multiple doses are administered prior to, simultaneously with and/or subsequent to the administration of the epoxytigliane compound.
29. The method according to claim 13 wherein the immune checkpoint inhibitor is selected from an anti-PD-1 antibody and an anti-CTLA4 antibody.