Solid forms of a toll-like receptor modulator
The present disclosure provides solid forms, solvates and hydrates of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol, and methods of making.
1. A crystalline form of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol gentisic acid:
characterized by an X-ray powder diffraction (XRPD) pattern comprising three or more peaks at 4.4°, 8.7°, 12.9°, 14.9°, 17.3°, 19.5°, 24.8°, 25.7°, or 26.3° 2θ (±0.2° 2θ), Compound I gentisic acid.
2. The crystalline form of claim 1 , characterized by an XRPD pattern comprising four or more peaks at 4.4°, 8.7°, 12.9°, 14.9°, 17.3°, 19.5°, 24.8°, 25.7°, or 26.3° 2θ (±0.2° 2θ).
3. The crystalline form of claim 1 , characterized by an XRPD pattern comprising peaks at 4.4°, 8.7°, and 14.9° 2θ (±0.2° 2θ).
4. The crystalline form of claim 3 , wherein the XRPD pattern further comprises one or more additional peaks at 12.9°, 17.3°, 19.5°, 24.8°, 25.7°, or 26.3° 2θ (±0.2° 2θ).
5. The crystalline form of claim 3 , wherein the XRPD pattern further comprises two or more additional peaks at 12.9°, 17.3°, 19.5°, 24.8°, 25.7°, or 26.3° 2θ (±0.2° 2θ).
6. The crystalline form of claim 1 , characterized by an XRPD pattern comprising peaks at 12.9°, 24.8°, and 25.7° 2θ (±0.2° 2θ).
7. The crystalline form of claim 6 , wherein the XRPD pattern further comprises one or more additional peaks at 4.4°, 8.7°, 14.9°, 17.3°, 19.5°, or 26.3° 2θ (±0.2° 2θ).
8. The crystalline form of claim 6 , wherein the XRPD pattern further comprises two or more additional peaks at 4.4°, 8.7°, 14.9°, 24.8°, or 26.3° 2θ (±0.2° 2θ).
9. The crystalline form of claim 1 , characterized by an XRPD pattern comprising peaks at 4.4°, 8.7°, 12.9°, 14.9°, 17.3°, 19.5°, 24.8°, 25.7°, and 26.3° 2θ (±0.2° 2θ).
10. The crystalline form of claim 1 , characterized by an XRPD pattern substantially as shown in FIG. 2 .
11. The crystalline form of claim 1 , characterized by a differential scanning calorimetry (DSC) thermogram having an endotherm with an onset of about 178° C.
12. The crystalline form of claim 1 , characterized by a DSC thermogram substantially as shown in FIG. 3 .
13. A crystalline form of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol hippuric acid:
characterized by an XRPD pattern comprising three or more peaks at 2.9°, 5.0°, 7.6°, 10.4°, 12.6°, 17.6°, 19.0°, 25.2°, or 28.5° 2θ (±0.2° 2θ), Compound I hippuric acid.
14. A crystalline form of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol phosphoric acid:
characterized by an XRPD pattern comprising three or more peaks at 3.7°, 6.1°, 7.1°, 12.1°, 14.2°, 21.6°, 24.0°, 27.4°, or 28.2° 2θ (±0.2° 2θ), phosphate salt Form I.
15. A crystalline form of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol phosphoric acid:
characterized by an XRPD pattern comprising three or more peaks at 5.4°, 6.3°, 15.8°, 18.1°, 18.9°, 20.6°, 24.1°, 26.7°, or 27.4° 2θ (±0.2° 2θ), phosphate salt Form II.
16. A crystalline form of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol succinic acid:
characterized by an XRPD pattern comprising three or more peaks at 4.6°, 6.8°, 9.3°, 13.2°, 17.5°, 18.7°, 19.0°, 25.7°, or 27.0° 2θ (±0.2° 2θ), Compound I succinic acid.
17. A crystalline form of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol ethanedisulfonic acid:
characterized by an XRPD pattern comprising three or more peaks at 4.4°, 7.9°, 8.7°, 13.0°, 16.6°, 20.6°, 21.1°, 22.1°, or 26.0° 2θ (±0.2° 2θ), Compound I ethanedisulfonic acid Form I.
18. A crystalline form of (R)-2-((2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino)-2-methylhexan-1-ol ethanedisulfonic acid:
characterized by an XRPD pattern comprising three or more peaks at 4.5°, 5.6°, 8.4°, 12.9°, 13.4°, 16.6°, 17.9°, 18.3°, or 22.2° 2θ (±0.2° 2θ), Compound I ethanedisulfonic acid Form II.
19. A pharmaceutical composition comprising the crystalline form of claim 1 and one or more pharmaceutically acceptable excipients.
20. The pharmaceutical composition of claim 19 , wherein the crystalline form is the gentisate salt.
21. A method of treating or preventing a hepatitis B virus (HBV) infection in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the crystalline form of claim 1 , or the pharmaceutical composition of claim 19 .
22. The method of claim 21 , further comprising administering a therapeutically effective amount of one or more additional therapeutic agents.
23. The method of claim 21 , wherein the one or more additional therapeutic agents are administered simultaneously with the crystalline form or the pharmaceutical composition.
24. The method of claim 21 , wherein the one or more additional therapeutic agents are selected from the group consisting of: HBV combination drugs, HBV vaccines, HBV DNA polymerase inhibitors, immunomodulators, toll-like receptor (TLR) modulators, interferon alpha receptor ligands, hyaluronidase inhibitors, hepatitis b surface antigen (HBsAg) inhibitors, cytotoxic T-lymphocyte-associated protein 4 (ipi4) inhibitors, cyclophilin inhibitors, HBV viral entry inhibitors, antisense oligonucleotide targeting viral mRNA, short interfering RNAs (siRNA) and ddRNAi endonuclease modulators, ribonucleotide reductase inhibitors, HBV E antigen inhibitors, covalently closed circular DNA (cccDNA) inhibitors, farnesoid X receptor agonists, HBV antibodies, CCR2 chemokine antagonists, thymosin agonists, cytokines, nucleoprotein modulators, retinoic acid-inducible gene 1 stimulators, NOD2 stimulators, phosphatidylinositol 3-kinase (PI3K) inhibitors, indoleamine-2, 3-dioxygenase (IDO) pathway inhibitors, PD-1 inhibitors, PD-L1 inhibitors, recombinant thymosin alpha-1 agonists, Bruton's tyrosine kinase (BTK) inhibitors, KDM inhibitors, HBV replication inhibitors, arginase inhibitors, and other HBV drugs.
25. The method of claim 21 , wherein the one or more additional therapeutic agents are selected from the group consisting of: adefovir, tenofovir disoproxil fumarate+emtricitabine, tenofovir disoproxil fumarate, entecavir, lamivudine, tenofovir alafenamide, tenofovir, tenofovir disoproxil, tenofovir alafenamide fumarate, tenofovir alafenamide hemifumarate, telbivudine, emtricitabine, peginterferon alfa-2b, interferon alpha 1b, interferon alpha 2b, pegylated interferon alpha-2a, interferon alfa-n1, ribavirin, interferon beta-1a, Bioferon, Ingaron, Inmutag, Algeron, Roferon-A, Oligotide, Zutectra, Shaferon, interferon alfa-2b, Alfaferone, interferon alfa-2b, Feron, interferon-alpha 2, Bevac, Laferonum, Vipeg, Blauferon-B, Blauferon-A, Intermax Alpha, Realdiron, Lanstion, Pegaferon, PDferon-B, alfainterferona 2b, Kalferon, Pegnano, Feronsure, PegiHep, Optipeg A, Realfa 2B, Reliferon, peginterferon alfa-2b, Reaferon-EC, Proquiferon, Uniferon, Urifron, interferon alfa-2b, Anterferon, Shanferon, MOR-22, interleukin-2 (IL-2), recombinant human interleukin 2, Layfferon, Ka Shu Ning, Shang Sheng Lei Tai, Intefen, Sinogen, Fukangtai, Alloferon and celmoleukin.
26. The method of claim 21 , wherein the one or more additional therapeutic agents are selected from the group consisting of: entecavir, adefovir, tenofovir disoproxil fumarate, tenofovir alafenamide, tenofovir, tenofovir disoproxil, tenofovir alafenamide fumarate, tenofovir alafenamide hemifumarate, telbivudine and lamivudine.
27. The method of claim 21 , wherein the one or more additional therapeutic agents are selected from the group consisting of tenofovir alafenamide, tenofovir alafenamide fumarate, and tenofovir alafenamide hemifumarate.