IP Library Granted Patent US 10,233,154
Granted Patent B2
US 10,233,154 · App. 15/918,868 · Granted Mar 19, 2019

Crystalline forms of an NK-1 antagonist

Inventors: Christian Bacilieri (Breganzona, CH); Gionata Frasca (Minusio, CH)
Assignee: Helsinn Healthcare SA
C07D213/75
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Quick Facts
Patent No.
US 10,233,154
App. No.
15/918,868
Granted
Mar 19, 2019
Kind
B2
Abstract

The present invention is related to crystalline forms of 2-(3,5-bis(trifluoromethyl)phenyl)-N,2-dimethyl-N-(6-(4-methylpiperazin-1-yl)-4-(o-tolyl)pyridin-3-yl)propanamide which is an NK-1 antagonist useful in the treatment of induced vomiting and other disorders.

Claims (7)

1. A non-solvated micronized crystalline free-base form of the compound 2-(3,5-bis(trifluoromethyl)phenyl)-N,2-dimethyl-N-(6-(4-methylpiperazin-1-yl)-4-(o-tolyl)pyridin-3-yl)propanamide which is Form I, having an X-ray powder diffraction pattern comprising at least one peak, in terms of 20 at 4.5°±0.2°.

2. The crystalline form of claim 1 , having an X-ray powder diffraction pattern comprising the following peaks, in terms of 2θ: 4.5°±0.2°; 11.5°±0.2°; and 13.1°±0.2°.

3. The crystalline form of claim 1 , having an X-ray powder diffraction pattern comprising the following peaks, in terms of 2θ: 4.5°±0.2°; 8.4°±0.2°; 11.5°±0.2°; 13.1°±0.2°; 13.9°±0.2°; 14.8°±0.2°; 16.7°±0.2°; 17.4°±0.2°; 17.7°±0.2°; 19.5°±0.2°; 21.2°±0.2°; 21.6°±0.2°; and 21.8°±0.2°.

4. The crystalline form of claim 1 which is substantially isolated.

5. A pharmaceutical composition comprising a non-solvated crystalline micronized free-base form of the compound 2-(3,5-bis(trifluoromethyl)phenyl)-N,2-dimethyl-N-(6-(4-methylpiperazin-1-yl)-4-(o-tolyl)pyridin-3-yl)propanamide which is Form I, having an X-ray powder diffraction pattern comprising at least one peak, in terms of 20 at 4.5°±0.2°, and one or more pharmaceutically acceptable excipients.

6. The pharmaceutical composition of claim 5 , wherein the crystalline form has an X-ray powder diffraction pattern comprising the following peaks, in terms of 2θ: 4.5°±0.2°; 11.5°±0.2°; and 13.1°±0.2°.

7. The pharmaceutical composition of claim 5 , wherein the crystalline form has an X-ray powder diffraction pattern comprising the following peaks, in terms of 2θ: 4.5°±0.2°; 8.4°±0.2°; 11.5°±0.2°; 13.1°±0.2°; 13.9°±0.2°; 14.8°±0.2°; 16.7°±0.2°; 17.4°±0.2°; 17.7°±0.2°; 19.5°±0.2°; 21.2°±0.2°; 21.6°±0.2°; and 21.8°±0.2°.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Sep 20, 2023
From: HAMILTON SA LLC
To: HELSINN HEALTHCARE SA; HELSINN THERAPEUTICS (U.S.), INC.; HELSINN BIREX PHARMACEUTICALS LIMITED
Reel/Frame 064961/0567 →
SECURITY INTEREST Recorded Dec 30, 2022
From: HELSINN HEALTHCARE SA; HELSINN THERAPEUTICS (U.S.), INC.; HELSINN BIREX PHARMACEUTICALS LIMITED
To: HAMILTON SA LLC
Reel/Frame 062254/0888 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2018
From: BACILIERI, CHRISTIAN; FRASCA, GIONATA
To: HELSINN HEALTHCARE SA
Reel/Frame 045212/0825 →
Continuity (3)
Continuation 14865370 · Sep 25, 2015
Provisional Application 62055836 · Sep 26, 2014
Related Publication 20180201581A1 · Jul 19, 2018
Cited By (1)
US 12,606,527