Salts of a PD-1/PD-L1 inhibitor
The present invention relates to salt forms of the PD-1/PD-L1 inhibitor (R)-1-((7-cyano-2-(3′-(3-(((R)-3-hydroxypyrrolidin-1-yl)methyl)-1,7-naphthyridin-8-ylamino)-2,2′-dimethylbiphenyl-3-yl)benzo[d]oxazol-5-yl)methyl)pyrrolidine-3-carboxylic acid, including methods of preparation thereof, where the compound is useful in the treatment of various diseases including infectious diseases and cancer.
1. A salt, wherein the salt is
(R)-1-((7-cyano-2-(3′-(3-(((R)-3-hydroxypyrrolidin-1-yl)methyl)-1,7-naphthyridin-8-ylamino)-2,2′-dimethylbiphenyl-3-yl)benzo[d]oxazol-5-yl)methyl)pyrrolidine-3-carboxylic acid di-oxalic acid salt, and wherein the salt is crystalline.
2. The salt of claim 1 , having an X-ray powder diffraction pattern as substantially shown in FIG. 10 .
3. The salt of claim 1 , having a DSC thermogram substantially as depicted in FIG. 11 .
4. The salt of claim 1 , having a thermogravimetric analysis (TGA) thermogram substantially as depicted in FIG. 12 .
5. The salt of claim 1 , having at least one X-ray powder diffraction (XRPD) peak selected from 7.0±0.2, 11.4±0.2, 13.2±0.2, 14.9±0.2, and 17.0±0.2 degrees 2-theta.
6. The salt of claim 1 , having at least two X-ray powder diffraction (XRPD) peaks selected from 7.0±0.2, 11.4±0.2, 13.2±0.2, 14.9±0.2, and 17.0±0.2 degrees 2-theta.
7. The salt of claim 1 , having at least three X-ray powder diffraction (XRPD) peaks selected from 7.0±0.2, 11.4±0.2, 13.2±0.2, 14.9±0.2, and 17.0±0.2 degrees 2-theta.
8. The salt of claim 1 , having at least four X-ray powder diffraction (XRPD) peaks selected from 7.0±0.2, 11.4±0.2, 13.2±0.2, 14.9±0.2, and 17.0±0.2 degrees 2-theta.
9. The salt of claim 1 , having characteristic X-ray powder diffraction (XRPD) peaks at 7.0±0.2, 11.4±0.2, 13.2±0.2, 14.9±0.2, and 17.0±0.2 degrees 2-theta.
10. The salt of claim 1 , having a characteristic X-ray powder diffraction (XRPD) peak at 7.0±0.2 degrees 2-theta.
11. The salt of claim 1 , having a characteristic X-ray powder diffraction (XRPD) peak at 11.4±0.2 degrees 2-theta.
12. The salt of claim 1 , having a characteristic X-ray powder diffraction (XRPD) peak at 13.2±0.2 degrees 2-theta.
13. The salt of claim 1 , having a characteristic X-ray powder diffraction (XRPD) peak at 14.9±0.2 degrees 2-theta.
14. The salt of claim 1 , having a characteristic X-ray powder diffraction (XRPD) peak at 17.0±0.2 degrees 2-theta.
15. The salt of claim 1 , having an endothermic peak at a temperature of 235±3° C. in a differential scanning calorimetry (DSC) thermogram.
16. A pharmaceutical composition comprising a salt of claim 1 , and a pharmaceutically acceptable carrier or excipient.
17. A solid oral dosage form comprising the pharmaceutical composition of claim 16 .
18. A method of inhibiting PD-1/PD-L1 interaction, said method comprising administering to a patient a salt of claim 1 .
19. A method of treating a disease or disorder associated with inhibition of PD-1/PD-L1 interaction, said method comprising administering to a patient in need thereof a therapeutically effective amount of a salt of claim 1 .
20. A method of enhancing, stimulating and/or increasing the immune response in a patient, said method comprising administering to the patient in need thereof a therapeutically effective amount of a salt of claim 1 .
21. The method according to claim 19 , wherein the disease or disorder is cancer or infection diseases.
22. The method according to claim 21 , wherein the disease or disorder is cancer.
23. The method according to claim 22 , wherein the cancer is selected from a metastatic cancer that expresses PD-L1, lung cancer, small cell lung cancer, non-small cell lung cancer, hepatic cancer, hepatocellular carcinoma, melanoma, cancer of the bladder, cancer of the urethra, renal cancer, renal clear cell carcinoma, and cutaneous squamous cell carcinoma.