SUSTAINED RELEASE AMINOPYRIDINE COMPOSITION
A pharmaceutical composition which comprises a therapeutically effective amount of a aminopyridine dispersed in a release matrix, including, for example, a composition that can be formulated into a stable, sustained-release oral dosage formulation, such as a tablet which provides, upon administration to a patient, a therapeutically effective plasma level of the aminopyridine for a period of at least 12 hours, preferably 24 hours or more and the use of the composition to treat various neurological diseases.
1 .- 5 . (canceled)
6 . A process for preparing a sustained release 4-aminopyridine composition comprising the steps of:
a. Dry blending about 10 mg of 4-aminopyridine particles having a particles size distribution such that 90% of the particles are smaller than 300 microns, 50% of the particles are smaller than 150 microns and 10% of the particles are smaller than 50 microns, with a rate-controlling polymer for about 10 to about 55 minutes to form a blend; and
b. Compressing the blend formed in step a. to form one or more tablets.
7 . A 4-aminopyridine composition produced according to the process of claim 1 , wherein said composition upon administration to a human subject provides a CavSS of about 15 ng/ml to about 35 ng/ml.