Claims for Patent: 11,160,795

Summary for Patent: 11,160,795

Title:	Methods of treating tuberous sclerosis complex with cannabidiol and everolimus
Abstract:	The present disclosure provides methods of treating tuberous sclerosis complex comprising administering cannabidiol and everolimus.
Inventor(s):	Guy; Geoffrey (Cambridge, GB), Knappertz; Volker (Cambridge, GB), Dunayevich; Eduardo (Cambridge, GB), Critchley; David (Cambridge, GB)
Assignee:	GW Research Limited (Cambridge, GB)
Application Number:	17/188,766
Patent Claims:	1. A method of treating seizures in a human suffering from tuberous sclerosis complex comprising: (a) co-administering therapeutically effective amounts of everolimus and cannabidiol to the human suffering from a tuberous sclerosis complex; (b) monitoring the blood plasma concentrations of everolimus in the human suffering from the tuberous sclerosis complex; (c) if the human suffering from the tuberous sclerosis complex's blood plasma trough concentrations of everolimus exceed 15 ng/mL, if the Cmax exceeds 50 ng/mL, or if the AUC 0-24 exceeds 500 h*ng/mL; then (d) reducing the everolimus administered in step (a) to the human suffering from the tuberous sclerosis complex by at least 10%; wherein said monitoring in step (b) occurs one week to two weeks after the human suffering from the tuberous sclerosis complex begins receiving everolimus, and wherein the cannabidiol is synthetic or purified. 2. The method of claim 1, wherein the amount of cannabidiol is administered in step (a) in an amount ranging from about 5 mg/kg/day to about 25 mg/kg/day. 3. The method of claim 1, wherein the amount of cannabidiol is administered in step (a) at about 25 mg/kg/day. 4. The method of claim 1, wherein the amount of cannabidiol is administered in step (a) at about 20 mg/kg/day. 5. The method of claim 1, wherein the amount of cannabidiol is administered in step (a) at about 15 mg/kg/day. 6. The method of claim 1, wherein the amount of cannabidiol is administered in step (a) at about 10 mg/kg/day. 7. The method of claim 1, wherein the cannabidiol is synthetic. 8. The method of claim 1, wherein the cannabidiol is purified. 9. The method of claim 8, wherein the cannabidiol has a purity of at least 95% (w/w). 10. The method of claim 8, wherein the cannabidiol has a purity of at least 98% (w/w). 11. The method of claim 1, wherein the amount of everolimus is reduced by at least 10% if the human's suffering from tuberous sclerosis complex's blood plasma trough concentration of everolimus exceeds 15 ng/mL. 12. The method of claim 1, wherein the amount of everolimus is reduced by at least 10% if the human's suffering from tuberous sclerosis complex's Cmax of everolimus exceeds 50 ng/mL. 13. The method of claim 1, wherein the amount of everolimus is reduced by at least 10% if the human's suffering from tuberous sclerosis complex's AUC 0-24 exceeds 500 h*ng/mL. 14. The method of claim 1, wherein the seizures are generalized seizures. 15. The method of claim 14, wherein the generalized seizures are tonic-clonic, tonic, clonic or atonic seizures. 16. The method of claim 1, wherein the seizures are focal seizures. 17. The method of claim 16, wherein the focal seizures are focal motor seizures without impairment of consciousness or awareness, focal seizures with impairment of consciousness or awareness, focal seizures evolving to bilateral generalized convulsive seizures, or focal seizures evolving to generalized seizures. 18. The method of claim 1, wherein the administering reduces the total number of seizures compared to the number of seizures experienced during a baseline period before the cannabidiol was administered. 19. The method of claim 1, wherein the number seizures is reduced by at least 50% compared to the number of seizures experienced during a baseline period before the cannabidiol was administered. 20. The method of claim 1, wherein, in step (a), 5 mg/m.sup.2 of everolimus is administered once daily. 21. The method of claim 1, wherein, in step (a), 4.5 mg/m.sup.2 everolimus is administered once daily. 22. The method of claim 1, wherein, in step (a), 10 mg everolimus is administered once daily. 23. The method of claim 1, wherein the amount of everolimus in step (d) is reduced by about 10% to about 50%. 24. The method of claim 1, wherein about 2.5 mg/m.sup.2 to about 4.5 mg/m.sup.2 of everolimus is administered in step id). 25. The method of claim 1, wherein about 2.3 mg/m.sup.2 to about 4.1 mg/m.sup.2 of everolimus is administered in step id). 26. The method of claim 1, wherein about 5 mg to about 9 mg of everolimus is administered in step id). 27. The method of claim 1, about 2.5 mg/m.sup.2, about 3.0 mg/m.sup.2, about 3.5 mg/m.sup.2, about 4.0 mg/m.sup.2, or about 4.1 mg/m.sup.2 of everolimus is administered in step (d). 28. The method of claim 1, about 2.5 mg/m.sup.2, about 3.0 mg/m.sup.2, about 3.5 mg/m.sup.2, about 4.0 mg/m.sup.2, about 4.1 mg/m.sup.2 or about 4.5 mg/m.sup.2 of everolimus is administered in step (d). 29. The method of claim 1, wherein about 2 mg, about 2.5 mg, about 3 mg, about 3.5 mg, about 4 mg, about 4.5 mg, about 5.0 mg, about 5.5 mg, about 6.0 mg, about 6.5 mg, about 7.0 mg, about 7.5 mg, about 8.0 mg, about 8.5 mg, about 9.0 mg, or about 9.5 mg of everolimus is administered in step (d).