Aqueous oral pharmaceutical suspension compositions
Provided is an aqueous oral pharmaceutical suspension composition comprising vamorolone Form I. Also provided are methods for its preparation and its use.
1. A method of treating or reducing the symptoms of muscular dystrophy, comprising the administration, to a patient in need thereof, of a therapeutically effective amount of an aqueous oral pharmaceutical suspension composition comprising vamorolone Form I, at least one suspending agent, and at least one suspension vehicle.
2. The method of claim 1 , wherein the therapeutically effective amount is between 10 mg to 200 mg.
3. The method of claim 1 , wherein the therapeutically effective amount is between 0.01 mg/kg to 10.0 mg/kg.
4. The method of claim 1 , wherein the therapeutically effective amount is between 2 mg/kg to 6.0 mg/kg.
5. The method of claim 1 , wherein the muscular dystrophy chosen from Duchenne muscular dystrophy, Becker muscular dystrophy, limb girdle muscular dystrophy, congenital muscular dystrophy, facioscapulohumeral muscular dystrophy, myotonic muscular dystrophy, oculopharyngeal muscular dystrophy, distal muscular dystrophy, and Emery-Dreifuss muscular dystrophy.
6. A method of treating or reducing the symptoms of muscular dystrophy, comprising the administration, to a patient in need thereof, of a therapeutically effective amount of a crystalline form of vamorolone characterized by one or more of the following:
(a) an X-ray powder diffraction pattern comprising two or more peaks, in terms of ° 2θ, at about 11.9, about 13.7, about 16.1, and about 18.3 with radiation Cu Kα;
(b) an X-ray powder diffraction pattern substantially as shown in FIG. 1 ;
(c) a thermogravimetric analysis profile showing less than about 0.5% weight loss below about 175° C.;
(d) a thermogravimetric analysis profile substantially as shown in FIG. 2 ;
(e) an exothermic event onset at 180.7° C. and a melting event with an onset and peak temperatures of 231.0° C. and 234.7° C., respectively, as measured by differential scanning calorimetry; and
(f) a differential scanning calorimetry trace substantially as shown in FIG. 3 .
7. The method of claim 6 , wherein the muscular dystrophy chosen from Duchenne muscular dystrophy, Becker muscular dystrophy, limb girdle muscular dystrophy, congenital muscular dystrophy, facioscapulohumeral muscular dystrophy, myotonic muscular dystrophy, oculopharyngeal muscular dystrophy, distal muscular dystrophy, and Emery-Dreifuss muscular dystrophy.
8. The method of claim 1 , wherein the suspension comprises vamorolone Form I in an amount of about 4% w/w.
9. The method of claim 1 , where in the suspension has a strength of 40 mg/mL.
10. The method of claim 4 , wherein the therapeutically effective amount is 6 mg/kg per day.
11. The method of claim 4 , wherein the therapeutically effective amount is 2 mg/kg per day.
12. The method of claim 5 , wherein the muscular dystrophy is Duchenne muscular dystrophy.
13. The method of claim 6 , wherein the suspension comprises vamorolone Form I in an amount of about 4% w/w.
14. The method of claim 6 , where in the suspension has a strength of 40 mg/mL.
15. The method of claim 6 , wherein the therapeutically effective amount is between 2 mg/kg to 6.0 mg/kg.
16. The method of claim 7 , wherein the muscular dystrophy is Duchenne muscular dystrophy.
17. A method of treating or reducing the symptoms of a disease chosen from chronic obstructive pulmonary disease, asthma, arthritis, Crohn's disease, inflammatory bowel disease, heart disease, multiple sclerosis, glioma, Behçet's disease, Henoch-Schönlein purpura polyarteritis nodosa, polymyositis, dermatomyositis, Wegener's granulomatosis, and graft-versus-host disease, comprising the administration, to a patient in need thereof, of a therapeutically effective amount of an aqueous oral pharmaceutical suspension composition comprising vamorolone Form I, at least one suspending agent, and at least one suspension vehicle.
18. The method of claim 17 , wherein the therapeutically effective amount is between 10 mg to 200 mg.
19. The method of claim 17 , wherein the therapeutically effective amount is between 0.01 mg/kg to 10.0 mg/kg.
20. The method of claim 17 , wherein the therapeutically effective amount is between 2 mg/kg to 6.0 mg/kg.
21. A method of treating or reducing the symptoms of a disease chosen from chronic obstructive pulmonary disease, asthma, arthritis, Crohn's disease, inflammatory bowel disease, heart disease, multiple sclerosis, glioma, Behçet's disease, Henoch-Schönlein purpura, polyarteritis nodosa, polymyositis, dermatomyositis, Wegener's granulomatosis, and graft-versus-host disease, comprising the administration, to a patient in need thereof, of a therapeutically effective amount of a crystalline form of vamorolone characterized by one or more of the following:
(g) an X-ray powder diffraction pattern comprising two or more peaks, in terms of ° 2θ, at about 11.9, about 13.7, about 16.1, and about 18.3 with radiation Cu Kα;
(h) an X-ray powder diffraction pattern substantially as shown in FIG. 1 ;
(i) a thermogravimetric analysis profile showing less than about 0.5% weight loss below about 175° C.;
(j) a thermogravimetric analysis profile substantially as shown in FIG. 2 ;
(k) an exothermic event onset at 180.7° C. and a melting event with an onset and peak temperatures of 231.0° C. and 234.7° C., respectively, as measured by differential scanning calorimetry; and
(l) a differential scanning calorimetry trace substantially as shown in FIG. 3 .