US2019381049A1PendingUtilityA1
Compositions and methods for treating dementia
Est. expiryApr 21, 2036(~9.8 yrs left)· nominal 20-yr term from priority
Inventors:John Jahangir Alam
A61P 25/28A61K 31/519A61K 31/5025
51
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Claims
Abstract
The present invention provides methods and compositions for improving episodic memory and treating dementia.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of improving episodic memory in a human subject that has dementia, the method comprising administering to a subject in need thereof a therapeutically effective amount of VX-745.
2 . The method of claim 1 , wherein the therapeutically effective amount of VX-745 provides an average blood concentration of about 8 ng/mL.
3 . The method of claim 1 , wherein the therapeutically effective amount is achieved by twice daily administration.
4 . The method of claim 3 , wherein the twice daily administering occurs about 9 to 15 hours apart.
5 . The method of claim 1 , wherein the administering occurs within about 30 to 60 minutes after the subject consumes food.
6 . The method of claim 1 wherein an improvement in episodic memory is measured by the Wechsler Memory Scale (WMS).
7 . The method of claim 1 wherein an improvement in episodic memory is measured by the Mini-Mental State Examination (MMSE).
8 . The method of claim 7 , wherein the human subject has a baseline MMSE score from about 20 to about 28 prior to treatment.
9 . The method of claim 7 , wherein the treating of the human subject results in at least a 3 point increase over the baseline MMSE score.
10 . A method of treating dementia in a human subject exhibiting a decline in at least two of the following:
memory; communication and language; ability to focus and pay attention; reasoning and judgment; and visual perception;
the method comprising administering to a subject in need thereof a therapeutically effective amount of VX-745.
11 . The method of claim 10 , wherein the therapeutically effective amount of VX-745 provides an average blood concentration of about 8 ng/mL.
12 . The method of claim 10 , wherein the therapeutically effective amount is achieved by twice daily administration.
13 . The method of claim 12 , wherein the twice daily administering occurs about 9 to 15 hours apart.
14 . The method of claim 10 , wherein the administering occurs within about 30 to 60 minutes after the subject consumes food.
15 . The method of claim 10 , wherein VX-745 is administered at a dose of about 40 mg.
16 . A method of improving episodic memory in a human subject, the method comprising administering to a subject in need thereof a therapeutically effective amount of VX-745, wherein the subject has a neurodegenerative disorder characterized by an increase in the number and/or size of endosomes.
17 . The method of claim 16 , wherein the therapeutically effective amount of VX-745 provides an average blood concentration of about 8 ng/mL.
18 . The method of claim 16 , wherein the therapeutically effective amount is achieved by twice daily administration.
19 . The method of claim 18 , wherein the twice daily administering occurs about 9 to 15 hours apart.
20 . The method of claim 16 , wherein VX-745 is administered at a dose of about 40 mg.Cited by (0)
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