Pharmaceutical compositions comprising levodopa, a dopamine decarboxylase inhibitor and a COMT inhibitor and method of administration thereof
A pharmaceutical gel composition for intra-intestinal administration comprises (i) a dopamine replacement agent, (ii) a dopamine decarboxylase inhibitor (DDI), and (iii) a COMT inhibitor.
1. A pharmaceutical composition for intra-intestinal administration, comprising:
a dopamine replacement agent selected from levodopa, melevodopa, etilevodopa and combinations thereof;
a dopamine decarboxylase inhibitor (DDI) wherein the dopamine decarboxylase inhibitor is carbidopa, benzerazide or combination thereof; and
a catechol-O-methyltransferase (COMT) inhibitor selected from entacapone, tolcapone, opicapone and combinations thereof,
wherein the composition has a pH value equal to or lower than about 5.7.
2. The pharmaceutical composition of claim 1 , wherein the dopamine replacement agent is levodopa.
3. The pharmaceutical composition according to claim 1 , wherein the dopamine decarboxylase inhibitor is carbidopa.
4. The pharmaceutical composition according to claim 1 , wherein the COMT inhibitor is entacapone.
5. The pharmaceutical composition according to claim 1 , wherein the composition has a pH value from about 4.5 to about 5.5.
6. The pharmaceutical composition according to claim 1 , wherein the composition is deoxygenized.
7. The pharmaceutical composition according to claim 1 , wherein the composition further comprises an antioxidant.
8. The pharmaceutical composition according to claim 7 , wherein the antioxidant is ascorbic acid or citric acid.
9. The pharmaceutical composition according to claim 1 , wherein the composition is free from metal chelating agent.
10. The pharmaceutical composition according to claim 1 , wherein the composition is provided in a light-protected container.
11. The pharmaceutical composition according to claim 1 ,
wherein levodopa, the DDI and the COMT inhibitor are in the form of particles;
the particles are suspended in an aqueous carrier, and have the particle size no greater than 80 μm; and
the carrier has a viscosity of at least 300 mPas at a moderate shear rate.
12. The pharmaceutical composition according to claim 11 , wherein the carrier is polysaccharide selected from the group consisting of cellulose, methyl cellulose, ethyl cellulose, carboxymethyl cellulose, salts thereof, and combinations thereof.
13. The pharmaceutical composition according to claim 12 , wherein the carrier is sodium carboxymethyl cellulose.
14. The pharmaceutical composition according to claim 1 , wherein the composition comprises about 1.0 to about 15% (w/w) micronized levodopa, about 0.1 to about 2.0% (w/w) micronized carbidopa, about 1.0 to about 5.0% (w/w) micronized entacapone, and about 1.0 to about 7.5% (w/w) sodium carboxymethyl cellulose.
15. The pharmaceutical composition according to claim 11 , wherein the pH of the pharmaceutical composition is greater than about 5.0, and
the viscosity of the aqueous carrier after 12 days at 25° C. is at least about 300 mPas at a moderate shear rate.
16. The pharmaceutical composition according to claim 2 , wherein the weight ratio of the dopamine decarboxylase inhibitor to levodopa is about 1:10 to about 1:2, or about 1:5 to about 1:3.
17. The pharmaceutical composition according to claim 2 , wherein the weight ratio of the COMT inhibitor to levodopa is about 10:1 to about 2:1, or 5:1 to 3:1.
18. The pharmaceutical composition according to claim 2 , wherein the composition comprises at least about 10 mg/ml of levodopa, at least about 2.5 mg/ml of a dopamine decarboxylase inhibitor, and at least about 10 mg/ml of a COMT inhibitor.
19. The pharmaceutical composition according to claim 2 , wherein the weight ratio of the dopamine decarboxylase inhibitor to levodopa is at least about 1:10.
20. A method of treating Parkinson's Disease comprising administering intra-intestinally a pharmaceutical composition according claim 1 .