Stable pharmaceutical compositions of clonidine
The present invention relates to liquid pharmaceutical compositions of clonidine or its pharmaceutically acceptable salts thereof. Preferably, the liquid pharmaceutical compositions are suitable for oral administration, and are stable for extended periods of time. More specifically, stable liquid pharmaceutical compositions of clonidine at concentrations of 1 μg/mL or more are provided. The present invention further relates to stable oral liquid compositions of clonidine, methods for their administration, processes for their production, and use of these compositions for treatment of diseases treatable by clonidine.
1. A liquid pharmaceutical composition consisting of:
(a) clonidine hydrochloride at a concentration of about 20 μg/mL;
(b) stabilizer at a concentration of about 0.001% to 20% w/w, based on total weight of the composition;
(c) a preservative at a concentration of about 0.01% to 5.0% w/w, based on total weight of the composition;
(d) a sweetener;
(e) a flavoring agent; and
(f) water; and
(g) optionally, a pH adjusting agent;
wherein said composition is free of buffer;
wherein said composition is an oral solution; and
wherein not more than 2% w/w of total impurities are formed when said composition is stored for at least 3 months at 25° C./40% RH or 25° C./60% RH.
2. The liquid pharmaceutical composition according to claim 1 , wherein the said stabilizer is selected from the group consisting histidine, arginine, meglumine, tromethamine, sodium chloride or mixtures thereof.
3. The liquid pharmaceutical composition according to claim 1 , wherein the preservative is potassium sorbate and/or sodium propionate at a concentration of 2.5 mg/mL.
4. The liquid pharmaceutical composition according to claim 1 , wherein the sweetener is sucralose.
5. The liquid pharmaceutical composition according to claim 1 , wherein the pH is from about 3 to about 9.
6. The liquid pharmaceutical composition according to claim 1 , wherein the pH is from about 4 to about 6.
7. The liquid pharmaceutical composition according to claim 1 , wherein a concentration of the stabilizer is from 01% to 15.0% w/w, based on total weight of the composition.
8. The liquid pharmaceutical composition according to claim 1 , wherein a concentration of the stabilizer is from 0.1% to 10.0% w/w, based on total weight of the composition.
9. The liquid pharmaceutical composition according to claim 1 , wherein a weight ratio of clonidine hydrochloride to stabilizer ranges from about 1:50 to about 1:150.
10. The liquid pharmaceutical composition according to claim 1 , wherein a weight ratio of clonidine hydrochloride to stabilizer is about 1:125.
11. The liquid pharmaceutical composition according to claim 1 , wherein a concentration of the preservative ranges from 0.05% to 1.0%, based on total weight of the composition.
12. The liquid pharmaceutical composition according to claim 1 , wherein a weight ratio of clonidine hydrochloride to preservative is from about 1:20 to about 1:70.
13. The liquid pharmaceutical composition according to claim 1 , wherein a weight ratio of clonidine hydrochloride to preservative is about 1:50.
14. The liquid pharmaceutical composition according to claim 1 , wherein said composition exhibits in-use shelf life of at least one month when stored at room temperature.
15. A multi-dose container comprising the liquid pharmaceutical composition according to claim 1 .
16. A multi-dose container comprising the liquid pharmaceutical composition according to claim 15 , wherein the container is a polyethylene terephthalate (PET) bottle.
17. A multi-dose container comprising the liquid pharmaceutical composition according to claim 15 , wherein the container is a high-density polyethylene (HDPE) bottle.
18. A multi-dose container comprising the liquid pharmaceutical composition according to claim 15 , wherein the container is a glass bottle.
19. A multi-dose container comprising the liquid pharmaceutical composition according to claim 15 , wherein the container comprises blow-fill sealed vials.