Claims for Patent: 10,695,354
✉ Email this page to a colleague
Summary for Patent: 10,695,354
Title: | Methods of treatment of partial onset seizures using eslicarbazepine acetate |
Abstract: | The present disclosure relates to the treatment of various diseases and conditions with eslicarbazepine acetate. The present disclosure also relates to the use of eslicarbazepine acetate in a method for reducing or decreasing epileptic seizures in a patient. The present disclosure also relates to a method for increasing the exposure to eslicarbazepine in a patient. The present disclosure also relates to a method of preparing a pharmaceutical composition comprising eslicarbazepine acetate. |
Inventor(s): | de Almeida; Jose Luis (Arouca, PT), Soares da Silva; Patricio Manuel Vieira Ara (Oporto, PT) |
Assignee: | Bial-Portela & CA S.A. (Sao Mamede do Coronado, PT) |
Application Number: | 16/449,057 |
Patent Claims: |
1. A method for treating a patient with partial-onset seizures, comprising administering once-daily from about 800 mg to about 1800 mg of eslicarbazepine acetate to
the patient, wherein the patient is a human.
2. The method of claim 1, comprising administering once-daily at least about 1200 mg of eslicarbazepine acetate to the patient. 3. The method of claim 1, comprising administering once-daily at least about 1600 mg of eslicarbazepine acetate to the patient. 4. The method of claim 1, comprising administering once-daily from about 800 mg to about 1600 mg of eslicarbazepine acetate to the patient. 5. The method of claim 1, comprising administering once-daily about 800 mg of eslicarbazepine acetate to the patient. 6. The method of claim 1, comprising administering once-daily about 1200 mg of eslicarbazepine acetate to the patient. 7. The method of claim 1, comprising administering once-daily about 1600 mg of eslicarbazepine acetate to the patient. 8. The method of claim 1, wherein the eslicarbazepine acetate is in the form of one or more tablets or oral suspensions. 9. The method of claim 1, wherein the eslicarbazepine acetate is administered orally. 10. The method of claim 1, wherein steady-state plasma concentrations of eslicarbazepine are attained after 4 to 5 days of once-daily administration of the eslicarbazepine acetate. 11. The method of claim 1, wherein upon once-daily administration of the eslicarbazepine acetate, the number, duration, or frequency of seizures in the patient decreases relative to the number, duration, or frequency of seizures in a patient without treatment. 12. The method of claim 1, wherein the once-daily administration of the eslicarbazepine acetate results in a mean maximum plasma concentration, C.sub.max, of eslicarbazepine from about 18,700 ng/mL to about 47,700 ng/mL. 13. The method of claim 1, wherein the once-daily administration of the eslicarbazepine acetate results in an area under the concentration curve, AUC.sub.0-.tau., of eslicarbazepine from about 268,400 ngh/mL to about 740,300 ngh/mL, wherein .tau. is the dosing interval, which is 24 hours. 14. A method for treating a patient with refractory partial-onset seizures, comprising administering once-daily from about 800 mg to about 1800 mg of eslicarbazepine acetate to the patient, wherein the patient is a human experiencing at least four partial-onset seizures per month in spite of treatment with at least one other antiepileptic drug. 15. The method of claim 14, wherein the eslicarbazepine acetate is administered once-daily as adjunctive therapy to a patient being treated with at least one other anti-epileptic drug. 16. The method of claim 15, wherein the at least one other anti-epileptic drug is chosen from phenytoin, valproate, primidone, phenobarbital, lamotrigine, gabapentin, topiramate, clonazepam, and combinations thereof. 17. The method of claim 15, wherein the serum concentration of the at least one other anti-epileptic drug is not significantly decreased by the once-daily administration of the eslicarbazepine acetate. 18. The method of claim 14, comprising administering once-daily at least about 1200 mg of eslicarbazepine acetate to the patient. 19. The method of claim 14, comprising administering once-daily at least about 1600 mg of eslicarbazepine acetate to the patient. 20. The method of claim 14, comprising administering once-daily from about 800 mg to about 1600 mg of eslicarbazepine acetate to the patient. 21. The method of claim 14, comprising administering once-daily about 800 mg of eslicarbazepine acetate to the patient. 22. The method of claim 14, comprising administering once-daily about 1200 mg of eslicarbazepine acetate to the patient. 23. The method of claim 14, comprising administering once-daily about 1600 mg of eslicarbazepine acetate to the patient. 24. The method of claim 14, wherein the eslicarbazepine acetate is in the form of one or more tablets or oral suspensions. 25. The method of claim 14, wherein the eslicarbazepine acetate is administered orally. 26. The method of claim 1, wherein eslicarbazepine acetate is administered once-daily in an initial dose of about 400 mg and increased to a dose of about 800 mg, about 1200 mg, or about 1600 mg. 27. The method of claim 14, wherein eslicarbazepine acetate is administered once-daily in an initial dose of about 400 mg and increased to a dose of about 800 mg, about 1200 mg, or about 1600 mg. |
Make Better Decisions: Try a trial or see plans & pricing
Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.