Combinations comprising a pyrrolidine-2,5-dione IDO1 inhibitor and an anti-body

Patent metadata

Field	Value
Publication number	US-10945994-B2
Application number	US-201615573190-A
Country	US
Kind code	B2
Filing date	May 12, 2016
Priority date	May 14, 2015
Publication date	Mar 16, 2021
Grant date	Mar 16, 2021

Abstract

Combinations of an IDO1 inhibitor (e.g., a 3-(5-fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione compound), with an anti-PD1 antibody or anti-PD-L1 antibody, and an anti-4-1BB antibody, as selected anti-cancer or anti-viral agents are provided. Also provided are use of these combinations for the treatment and/or prevention of cancer and endometriosis.

First claim

The invention claimed is:

1. A combination regimen useful in cancer treatment comprising the co-administration to a subject in need thereof of (a) at least one indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor, (b) at least one second active component which is an immunomodulatory agent selected from an anti-PD-1 or anti-PD-L1 antibody, and (c) at least a third active component which is an anti-4-1BB antibody, wherein the IDO1 inhibitor is a racemic 3-(5-fluoro -1H-indol-3-yl) pyrrolidine-2,5-dione, the (R)- enantiomer thereof, the (S)-enantiomer thereof, or a mixture thereof.

2. The combination regimen according to claim 1 , wherein the IDO1 inhibitor and the anti-PD-1 or anti-PD-L1 antibody are administered to the subject substantially simultaneously.

3. The combination regimen according to claim 1 , wherein the IDO1 inhibitor and the anti-PD-1 or anti-PD-L1 antibody are delivered sequentially.

4. The combination regimen according to claim 1 , wherein the IDO1 inhibitor and the anti-PD-1 or anti-PD-L1 antibody are delivered via different routes.

5. The combination regimen according to claim 1 , wherein the IDO1 inhibitor is administered to the subject orally.

6. The combination regimen according to claim 1 , wherein the anti-PD-1 or anti-PD-L1 is administered to the subject via injection.

7. The combination regimen according to claim 1 , wherein the IDO1 inhibitor is selected from one or more of 3-(5-fluoro -1H-indol-3-yl)pyrrolidine-2,5-dione in free base form, 3-(5-fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione racemate, an (S)-enantiomer of 3-(5-fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione, or an (R)-enantiomer of 3-(5-fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione.

8. The combination regimen according to claim 7 , wherein the 3-(5-fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione racemate is used in the combination, said racemate comprising about 50% (R)- and (S)-enantiomers.

9. The combination regimen according to claim 7 , wherein a mixture of (R)- and (S)-enantiomers of 3-(5-fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione are used in the combination.

10. The combination regimen according to claim 9 , wherein greater than 50% of the (R)-enantiomer is used.

11. The combination regimen according to claim 9 , wherein the mixture of (R) and (S) enantiomers comprises at least 95% to 100% of the (R)-enantiomer.

12. The combination according to claim 1 , wherein the cancer is selected from malignant melanoma, acute myelogenous leukemia, pancreatic, colorectal, lung, prostate, cervical, brain, liver, head and neck, endometrial, ovarian cancers or breast cancer.

13. The combination according to claim 1 , wherein the subject has a chronic viral infection associated with oncogenesis.

14. The combination regimen according to claim 1 , wherein the cancer is breast cancer.

15. The combination regimen according to claim 1 , wherein the anti-PD-L1 antibody is avelumab.

16. The combination regimen according to claim 1 which comprises co-administration of a further active component which is an immunomodulatory agent selected from an anti-CTLA4 antibody, an anti-OX-40 antibody, an anti-cancer vaccine, an P-cadherin LP-Dual-Affinity Re-Targeting protein, a TDO inhibitor, a signal modulating inhibitor, an antibody-drug conjugate (ADC), ibrutinib or a chemotherapeutic.

17. The combination regimen according to claim 16 , wherein the immunomodulatory agent is an anti-CTLA4 antibody.

18. The combination regimen according to claim 17 , wherein the anti-CTLA4 antibody is ipilimumab or tremelimumab.

19. The combination regimen according to claim 16 , wherein the further active component is the anti-cancer vaccine.

20. The combination regimen according to claim 16 , wherein the further active component is the signal modulating inhibitor, wherein the signal modulating inhibitor is selected from a Pi3K/mTOR inhibitor, a Pi3K-alpha selective inhibitor, an MEK inhibitor, an enhancer of zeste homolog 2 (EZH2) inhibitor, an epidermal growth factor receptor (EGFR) inhibitor, a vascular endothelial growth factor (VEGF) inhibitor, or a selective inhibitor of the cyclin-dependent kinases CDK4 and CDK6.

21. The combination regimen according to claim 20 , wherein the signal modualting inhibitor is the Pi3k/mTOR inhibitor which is gedatolisib.

22. The combination regimen according to claim 20 , wherein the signal modulating inhibitor is a Pi3K-alpha selective inhibitor.

23. The combination regimen according to claim 20 , wherein the signal modulating inhibitor is the selective inhibitor of the cyclin-dependent kinases CDK4 and CDK6, which is palbociclib.

24. The combination regimen according to claim 16 , wherein the further active component is a chemotherapeutic which is an alkylating agent.

25. The combination regimen according to claim 24 , wherein the chemotherapeutic is temozolomide.

26. The combination regimen according to claim 24 , wherein the chemotherapeutic is docetaxel.

Assignees

• Pfizer
• Iteos Therapeutics

Inventors

• Kraus Manfred
• Cauwenberghs Sandra
• Crosignani Stefano
• Driessens Gregory

Classifications

• A61K31/495

  having six-membered rings with two {or more} nitrogen atoms as the only ring heteroatoms, e.g. piperazine {or tetrazines}(A61K31/48 takes precedence {; with three nitrogen atoms A61K31/53}) · CPC title

• A61K39/395

  Antibodies (agglutinins A61K38/36 {; as drug carriers A61K47/50}); Immunoglobulins; Immune serum, e.g. antilymphocytic serum · CPC title

• C07K16/2818

  against CD28 or CD152 · CPC title

• A61K31/519

  ortho- or peri-condensed with heterocyclic rings · CPC title

• A61K9/0053

  Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title