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Z-ARCHIVE-Cannabis

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Patent US10603290


Issued 2020-03-31

Formulation For Inhibiting Formation Of 5-ht2b Agonists And Methods Of Using Same

Drug combinations and their use are disclosed. A first drug is administered in combination with a second drug. The first drug such as fenfluramine is characterized by the formation of a metabolite including 5-HT2B agonists such as norfenfluramine with known adverse side effects. The second drug is in the form of a CYP inhibitor such as cannabidiol which modulates the formation of metabolite down thereby making the first drug safer.



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5 Independent Claims

  • 1. A method of reducing or ameliorating seizures in a patient, comprising: administering fenfluramine; and administering cannabidiol thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine.

  • 5. A method of reducing or ameliorating seizures in a patient diagnosed with a form of refractory epilepsy, comprising: administering a liquid formulation of fenfluramine to the patient in an amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day; and administering cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine.

  • 6. A method of reducing or ameliorating seizures in a patient diagnosed with a form of refractory epilepsy, comprising: administering a liquid formulation of fenfluramine to the patient in an amount which is 30% less than an effective amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day, due to co-administration of cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine.

  • 9. A method of reducing or ameliorating seizures patient diagnosed with Dravet syndrome, comprising: administering a liquid formulation of fenfluramine to the patient in an amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day; and administering cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine.

  • 10. A method of reducing or ameliorating seizures in a patient diagnosed with Dravet syndrome, comprising: administering a liquid formulation of fenfluramine to the patient in an amount which is 40% less than an effective amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day, due to co-administration of cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine.