IP Library › Granted Patent US 11,866,406
Granted Patent B2
US 11,866,406 · App. 17/847,736 · Granted Jan 9, 2024

Compositions of trofinetide

Inventors: Clive Blower (Doncaster East, AU); Mathew Peterson (San Diego, CA); James Murray Shaw (Parkdale, AU); James Anthony Bonnar (Ryde, AU); Etienne David Frank Philippe Moniotte (Waterloo, BE); Martin Bernard Catherine Bousmanne (Woluwe Saint-Labmert, BE); Cecilia Betti (Brussels, BE); Karel Willy Luc Decroos (Ghent, BE); Mimoun Ayoub (Staefa, CH)
Assignee: NEUREN PHARMACEUTICALS LIMITED
C07D207/16B01J21/06B01J21/18B01J23/44C07B2200/07
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Quick Facts
Patent No.
US 11,866,406
App. No.
17/847,736
Granted
Jan 9, 2024
Kind
B2
Abstract

This disclosure describes compounds of Formula (I), stereoisomers, side compounds thereof, pharmaceutical compositions and methods of manufacturing such compounds, using silylation reagents and producing compositions and products made using such methods. More particularly, this disclosure describes manufacture of trofinetide and side products, compositions and products containing such compounds, for pharmaceutical uses to treat neurodegenerative or neurodevelopmental disorders.

Claims (64)

1. A composition comprising a compound of Formula (I):

or a stereoisomer, or pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (II):

or a stereoisomer, or pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (III):

or a stereoisomer, or pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 and R 4 independently are selected from the group consisting of hydrogen and C 1-4 alkyl, provided at least one of R 1 , R 2 , R 3 and R 4 is C 1-4 alkyl.

2. The composition according to claim 1 , wherein the compound of Formula (I) is a compound of Formula (Ia):

or pharmaceutically acceptable salt thereof.

3. The composition according to claim 1 , wherein the compound of Formula (II) is a compound of Formula (IIa):

or pharmaceutically acceptable salt thereof.

4. The composition according to claim 1 , wherein the compound of Formula (III) is a compound of Formula (IX):

or pharmaceutically acceptable salt thereof.

5. The composition according to claim 1 , comprising the compound of Formula (III), wherein the compound according to Formula (III) is a compound of Formula (IIIa):

or pharmaceutically acceptable salt thereof.

6. The composition according to claim 2 comprising between about 97 wt % and about 100 wt % of the compound of Formula (Ia) on an anhydrous basis.

7. The composition according to claim 1 , wherein the compound according to Formula (III) is a compound of Formula (IV):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (V):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (VI):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (VII):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (VIII):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (IX):

or a stereoisomer, or pharmaceutically acceptable salt thereof.

8. The composition according to claim 2 , wherein said composition is obtained by:

a) coupling (2S)-2-methylpyrrolidine-2-carboxylic acid and benzyloxycarbonyl-glycine in the presence of an activating reagent, silylating agent and a solvent, or

b) coupling benzyloxycarbonyl-glycine and N-hydroxysuccinimide and then coupling the obtained benzyloxycarbonyl-glycine N-succinimidyl ester and (2S)-2-methylpyrrolidine-2-carboxylic acid in the absence or presence of an activating reagent, a solvent and in the absence or presence of a silylating agent;

c) coupling the obtained ((S)-1-(((benzyloxy)carbonyl)glycyl)-2-methylpyrrolidine-2-carboxylic acid) and (2S)-2-aminopentanedioic acid in the presence of an activating reagent, silylating agent and a solvent;

d) obtaining ((S)-1-(((benzyloxy)carbonyl)glycyl)-2-methylpyrrolidine-2-carbonyl)-L-glutamic acid; and

e) deprotecting ((S)-1-(((benzyloxy)carbonyl)glycyl)-2-methylpyrrolidine-2-carbonyl)-L-glutamic acid, to obtain a composition comprising the compound of Formula (Ia).

9. The composition according to claim 8 , wherein the compound according to Formula (II) is a compound of Formula (IIa):

or pharmaceutically acceptable salt thereof.

10. The composition according to claim 8 , wherein deprotecting is achieved by hydrogenation.

11. The composition according to claim 10 , wherein hydrogenation is performed in the presence of a Pd/C catalyst.

12. The composition according to claim 10 , wherein hydrogenation is performed in the presence of a Pd/Si catalyst.

13. The composition according to claim 10 , wherein the hydrogenation is performed using at least one solvent selected from the group consisting of water, ethyl acetate, isopropyl acetate, methanol, ethanol, isopropanol, or mixtures thereof.

14. A kit containing a dosage form comprising a compound of Formula (Ia):

or a pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (IIa):

or pharmaceutically acceptable salt thereof, and instructions for administration to a subject in need thereof.

15. The composition according to claim 1 , wherein the compound of Formula (II), or stereoisomer, or pharmaceutically acceptable salt thereof, is present in an amount between about 0.001 wt % and about 0.2 wt %; and the compound of Formula (III), or stereoisomer, or pharmaceutically acceptable salt thereof, is absent.

16. A composition according to claim 1 , comprising a compound of Formula (Ia):

or pharmaceutically acceptable salt thereof, between about 0.001 wt % and about 0.2 wt % of a compound of Formula (IIa):

or pharmaceutically acceptable salt thereof; and

between about 0.001 wt % and about 0.2 wt % of a compound of Formula (IIIa):

or pharmaceutically acceptable salt thereof.

17. A composition comprising a compound of Formula (I):

or a stereoisomer, or pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (III):

or a stereoisomer, or pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 and R 4 independently are selected from the group consisting of hydrogen and C 1-4 alkyl, provided at least one of R 1 , R 2 , R 3 and R 4 is C 1-4 alkyl.

18. The composition according to claim 17 , wherein the compound of Formula (I) is a compound of Formula (Ia):

or pharmaceutically acceptable salt thereof.

19. The composition according to claim 17 , wherein the compound according to Formula (III) is a compound of Formula (IV):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (V):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (VI):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (VII):

or a stereoisomer, or pharmaceutically acceptable salt thereof;

Formula (VIII):

or a stereoisomer, or pharmaceutically acceptable salt thereof; or

Formula (IX):

or a stereoisomer, or pharmaceutically acceptable salt thereof.

20. The composition according to claim 17 , wherein the compound of Formula (III), or stereoisomer, or pharmaceutically acceptable salt thereof, is present in an amount between about 0.001 wt % and about 0.2 wt %.

Assignments (19)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: MONIOTTE, ETIENNE DAVID FRANK PHILIPPE
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065638/0452 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: MONIOTTE, ETIENNE DAVID FRANK PHILIPPE
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065638/0518 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: BOUSMANNE, MARTIN BERNARD CATHERINE
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065638/0563 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: BETTI, CECILIA
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065638/0780 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: BETTI, CECILIA
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065638/0804 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: DECROOS, KAREL WILLY LUC
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065638/0844 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: DECROOS, KAREL WILLY LUC
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065638/0898 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: CORDEN PHARMA BRUSSELS S.A.
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065638/0975 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: AYOUB, MIMOUN
To: CORDEN PHARMA SWITZERLAND LLC
Reel/Frame 065639/0022 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: AYOUB, MIMOUN
To: CORDEN PHARMA SWITZERLAND LLC
Reel/Frame 065639/0046 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: CORDEN PHARMA SWITZERLAND LLC
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065639/0091 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: CORDEN PHARMA SWITZERLAND LLC
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065639/0233 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: PETERSON, MATTHEW
To: ACADIA PHARMACEUTICALS INC.
Reel/Frame 065639/0300 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: ACADIA PHARMACEUTICALS INC.
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065639/0323 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: ACADIA PHARMACEUTICALS INC.
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065639/0362 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: BOUSMANNE, MARTIN BERNARD CATHERINE
To: CORDEN PHARMA BRUSSELS S.A.
Reel/Frame 065639/0421 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: BLOWER, CLIVE; SHAW, JAMES MURRAY; BONNAR, JAMES ANTHONY
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065639/0499 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: BLOWER, CLIVE; SHAW, JAMES MURRAY; BONNAR, JAMES ANTHONY
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065659/0643 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2023
From: CORDEN PHARMA BRUSSELS S.A.
To: NEUREN PHARMACEUTICALS LIMITED
Reel/Frame 065659/0660 →
Continuity (4)
Continuation 17347135 · Jun 14, 2021
Continuation PCTUS2020044733 · Aug 3, 2020
Provisional Application 62882998 · Aug 5, 2019
Related Publication 20220324799A1 · Oct 13, 2022
Cited By (1)
US 12,297,172