Claims for Patent: 11,603,363

Summary for Patent: 11,603,363

Title:	Crystalline form of LNP023
Abstract:	Described herein is a crystalline hydrate form of LNP023 hydrochloride and to a process for its preparation. Furthermore, described herein is a pharmaceutical composition comprising the crystalline hydrate form of LNP023 hydrochloride, and at least one pharmaceutically acceptable excipient. The pharmaceutical composition described herein can be used to treat a disease and disorder mediated by complement activation.
Inventor(s):	Zichen JIA, Philipp Lustenberger, Marie Meyer, Massimo Moratto
Assignee:	Novartis AG
Application Number:	US17/322,409
Patent Claims:	1. A crystalline hydrate form of a compound having Formula (A) characterized by having a powder X-ray diffractogram comprising peaks at 2-Theta angles of (4.6±0.2)°, (9.2±0.2)° and (19.1±0.2)°, when measured at a temperature in the range of from 20 to 30° C. with Cu-Kalpha1,2 radiation having a wavelength of 0.15419 nm. 2. The crystalline hydrate form of claim 1, characterized by having a powder X-ray diffractogram comprising one or two peaks at 2-Theta angles of (6.8±0.2)° or (24.6±0.2)°, when measured at a temperature in the range of from 20 to 30° C. with Cu-Kalpha1,2 radiation having a wavelength of 0.15419 nm. 3. The crystalline hydrate form of claim 1, characterized by having a Fourier transform infrared spectrum comprising peaks at wavenumbers of (3452±2) cm−1, (2875±2) cm−1, (1692±2) cm−1, (1439±2) cm−1 and (1243±2) cm−1, when measured at a temperature in the range of from 20 to 30° C. with a diamond ATR cell. 4. The crystalline hydrate form of claim 1, characterized by having a differential scanning calorimetry curve comprising an endothermic event in the range of 35° C. to 170° C., when measured at a heating rate of 10 K/min. 5. The crystalline hydrate form of claim 1, characterized by having a thermogravimetric analysis curve showing a mass loss at a temperature of from 200 to 220° C., of not more than 4.5 w-%, based on the weight of the crystalline form, when heated from 30 to 300° C. at a rate of 20 K/min. 6. The crystalline hydrate form of claim 1, characterized by showing a mass change of not more than 4.5 w-%, based on the weight of the crystalline form at 0% RH, when measured with dynamic vapor sorption at a relative humidity in the range of from 0 to 95% and a temperature of (25±1.0)° C. 7. The crystalline hydrate form of claim 1, wherein the hydrate form is a monohydrate. 8. The crystalline hydrate form of claim 1, having a crystal habit which is essentially equant in shape. 9. A composition comprising the crystalline hydrate form of claim 1, wherein the composition comprises at most 20 weight %, 10 weight %, 5 weight %, 2 weight % or 1 weight % of any other physical form of the compound having Formula (A), based on the weight of the composition. 10. The composition according to claim 9, wherein the other physical form of the compound having Formula (A) is characterized by having a powder X-ray diffractogram comprising peaks at 2-Theta angles of (11.6±0.1)°, (15.3±0.1)°, (16.5±0.1)°, (20.1±0.1)° and (23.3±0.1)°, when measured at a temperature in the range of from 20 to 30° C. with Cu-Kalpha1,2 radiation having a wavelength of 0.15419 nm. 11. A pharmaceutical composition comprising the crystalline hydrate form of claim 1, and optionally at least one pharmaceutically acceptable excipient. 12. The pharmaceutical composition of claim 11, which is an oral solid dosage form. 13. The pharmaceutical composition of claim 11, comprising the crystalline hydrate form having an aspect ratio between from about 0.4 to about 0.7. 14. The pharmaceutical composition of claim 11, comprising the crystalline hydrate form having a particle size distribution X50 of from about 10 to about 70 μm. 15. The pharmaceutical composition of claim 11, comprising the crystalline hydrate form having a consolidated (15 kPa) bulk density from about 0.50 to about 0.65 g/ml. 16. The pharmaceutical composition of claim 11, wherein the composition comprises the compound having Formula (A) at a dose of up to about 200 mg, calculated as an anhydrous free base of the compound having Formula (A). 17. The pharmaceutical composition of claim 16, wherein the composition comprises the compound having Formula (A) at a dose of from about 10 mg to about 200 mg, calculated as the anhydrous free base of the compound having Formula (A). 18. The pharmaceutical composition of claim 16, wherein the composition comprises the compound having Formula (A) at a dose of about 10 mg, about 25 mg, about 50 mg, about 100 mg, or about 200 mg, each calculated as the anhydrous free base of the compound having Formula (A). 19. The pharmaceutical composition of claim 16, wherein the composition comprises the compound having Formula (A) at a dose of 10 mg, 25 mg, 50 mg, 100 mg, or 200 mg, each calculated as the anhydrous free base of the compound having Formula (A). 20. A process for preparing the crystalline hydrate form of claim 1, the process comprising: (i) providing the compound having Formula (A) in a solid form; (ii) suspending the compound having Formula (A) provided in step (i) in a first solvent comprising acetone and water and heating to dissolve the solid form to provide a solution; (iii) cooling the solution obtained in step (ii) and adding a second solvent comprising acetone, ethyl acetate, or a combination thereof, to provide crystals in a mother liquor; (iv) separating at least a part of the crystals obtained in step (iii) from the mother liquor to provide isolated crystals; (v) optionally washing the isolated crystals obtained in step (iv); and (vi) drying the crystals obtained in step (iv) or (v). 21. The process according to claim 20 comprising as step (iii) (a) cooling the solution obtained in step (ii) followed by re-heating the solution again; (b) repeating step (a) at least 3 times; and (c) adding a second solvent comprising acetone, ethyl acetate, or a combination thereof. 22. The crystalline hydrate form of claim 1, having a crystal habit which is columnar in shape. 23. The pharmaceutical composition of claim 11, which is a capsule.