IP Library › Granted Patent US 12,583,884
Granted Patent B2
US 12,583,884 · App. 17/414,826 · Granted Mar 24, 2026

3beta-(benzyloxy)-17alpha-methyl-pregn-5-en-20-one for use in the treatment of cognitive disorders

Inventors: Pier Vincenzo Piazza (Bordeaux, FR); Sandy Fabre (Bordeaux, FR); Stéphanie Monlezun (Bordeaux, FR); Mathilde Metna (Bordeaux, FR); Monique Vallee (Bordeaux, FR); Jean-Michel Revest (Bordeaux, FR); Daniela Cota (Bordeaux, FR); Giovanni Marsicano (Bordeaux, FR); Aline Marighetto (Bordeaux, FR); Andrés Ozaita (Barcelona, ES); Rafael Maldonado (Barcelona, ES)
Assignees: AELIS FARMA; UNIVERSITE DE BORDEAUX
C07J7/009A61P25/28
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Quick Facts
Patent No.
US 12,583,884
App. No.
17/414,826
Granted
Mar 24, 2026
Kind
B2
Abstract

The present invention generally relates to a specific pregnenolone derivative for its use for the treatment of a cognitive disorders. More particularly, the invention relates to a compound of Formula (I) for its use in the treatment of cognitive disorders. Indeed, the compound of the invention is in vivo very potent in correcting the cognitive impairments observed in cognitive disorders.

Claims (13)

1 . A method of treating a cognitive disorder, comprising administering to a human subject with Down syndrome or Fragile X syndrome and in need thereof a therapeutically effective amount of a compound according to Formula (I):

wherein the compound is administered to the subject at a dose of between 20 μg to 2 mg per day.

2 . The method of claim 1 , wherein the compound according to Formula (I) is administered to the subject by an oral route.

3 . The method of claim 1 , wherein the compound according to Formula (I) is administered to the subject by a parenteral route.

4 . The method of claim 1 , wherein the compound according to Formula (I) is administered to the subject by a route selected from the group consisting of an intravenous route, a subcutaneous route, an intranasal route, and an intramuscular route.

5 . The method of claim 1 , wherein the compound according to Formula (I) is administered to the subject at a dose of between 20 μg to 600 μg per day.

6 . The method of claim 1 , wherein the compound according to Formula (I) is administered to the subject at a dose of 100 μg per day.

7 . The method of claim 1 , wherein the compound according to Formula (I) is administered to the subject at a dose of 200 μg per day.

8 . The method of claim 1 , wherein the compound according to Formula (I) is administered to the subject at a dose of 600 μg per day.

9 . The method of claim 5 , wherein the compound according to Formula (I) is administered to the subject by an oral route.

10 . The method of claim 6 , wherein the compound according to Formula (I) is administered to the subject by an oral route.

11 . The method of claim 7 , wherein the compound according to Formula (I) is administered to the subject by an oral route.

12 . The method of claim 8 , wherein the compound according to Formula (I) is administered to the subject by an oral route.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2022
From: PIAZZA, PIER VINCENZO; FABRE, SANDY; MONLEZUN, STEPHANIE; METNA, MATHILDE; VALLEE, MONIQUE; REVEST, JEAN-MICHEL; COTA, DANIELA; MARSICANO, GIOVANNI; MARIGHETTO, ALINE; OZAITA, ANDRES; MALDONADO, RAFAEL
To: AELIS FARMA; UNIVERSITE DE BORDEAUX; INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
Reel/Frame 058596/0559 →
Priority Claims (1)
EP 18306716 · Dec 18, 2018 · regional
Continuity (1)
Related Publication 20220017562A1 · Jan 20, 2022
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