Neurodevelopmental disorder therapy
This invention addresses tetrahydro-N, N-dimethyl-2,2diphenyl-3-furanmethanamine hydrochloride (ANAVEX2-73, AV2-73, or A2-73) in a method of treatment for neurodevelopmental disorders. Particular reference is made to the treatment of autism spectrum disorder, cerebral palsy, Rett syndrome, Angelman syndrome, Williams syndrome, pervasive developmental disorder not otherwise specified (PDD-NOS), childhood disintegrative disorder, and Smith-Magenis syndrome. Additional reference is made to multiple sclerosis.
1 . A method of treating Rett syndrome in a subject by administering to said subject a composition comprising a therapeutically effective amount of tetrahydro-N, N-dimethyl-2,2-diphenyl-3-furanmethanamine hydrochloride (A2-73); wherein the therapeutically effective amount is a dosage from about 0.5 mg/day to about 100 mg/day; and wherein the composition is selected from an oral composition, a transdermal composition, a parenteral composition, and an intravenous composition.
2 . The method of claim 1 , wherein the composition is an oral composition and the dosage is from about 1 mg/day to about 60 mg/day.
3 . The method of claim 2 , wherein the composition is an oral composition and the dosage is from about 20 mg/day to about 50 mg/day.
4 . The method of claim 3 , wherein the composition is an oral composition and the dosage is from about 30 mg/day to about 40 mg/day.
5 . The method of claim 1 , wherein the composition is an oral composition and the dosage is from about 0.5 mg/day to about 20 mg/day.
6 . The method of claim 1 , wherein the composition is a transdermal composition and the dosage is from about 1 mg/day to about 60 mg/day.
7 . The method of claim 6 , wherein the composition is a transdermal composition and the dosage is from about 20 mg/day to about 50 mg/day.
8 . The method of claim 7 , wherein the composition is a transdermal composition and the dosage is from about 30 mg/day to about 40 mg/day.
9 . The method of claim 1 , wherein the composition is a transdermal composition and the dosage is from about 0.5 mg/day to about 20 mg/day.
10 . The method of claim 1 , wherein the composition is a parenteral composition and the dosage is from about 1 mg/day to about 60 mg/day.
11 . The method of claim 10 , wherein the composition is a parenteral composition and the dosage is from about 20 mg/day to about 50 mg/day.
12 . The method of claim 11 , wherein the composition is a parenteral composition and the dosage is from about 30 mg/day to about 40 mg/day.
13 . The method of claim 1 , wherein the composition is a parenteral composition and the dosage is from about 0.5 mg/day to about 20 mg/day.
14 . The method of claim 1 , wherein the composition is an intravenous composition and the dosage is from about 1 mg/day to about 60 mg/day.
15 . The method of claim 14 , wherein the composition is an intravenous composition and the dosage is from about 20 mg/day to about 50 mg/day.
16 . The method of claim 14 , wherein the composition is an intravenous composition and the dosage is from about 30 mg/day to about 40 mg/day.
17 . The method of claim 1 , wherein the composition is an intravenous composition and the dosage is from about 0.5 mg/day to about 20 mg/day.
18 . The method of claim 1 , wherein the composition is administered to the subject for a period of at least 5 days, at least 10 days, at least 15 days, at least 60 days, at least 6 months, a least 1 year, at least 2 years, at least 3 years, at least 4 years, or at least 5 years.
19 . The method of claim 6 , wherein administering the transdermal composition comprises use of a transdermal device.
20 . The method of claim 19 , wherein the transdermal device comprises a transdermal patch selected from a reservoir membrane type patch, a porous membrane type patch, or a solid matrix type patch.