IP Library Granted Patent US 9,889,119
Granted Patent B2
US 9,889,119 · App. 15/498,787 · Granted Feb 13, 2018

Amorphous tecovirimat preparation

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,889,119
App. No.
15/498,787
Granted
Feb 13, 2018
Kind
B2
Abstract

Disclosed are methods for the preparation of amorphous N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindo1-2(1H)-yl]-4-(trifluoromethyl)-benzamide for the treatment or prophylaxis of viral infections and diseases associated therewith, particularly those viral infections and associated diseases caused by the orthopoxvirus. Also disclosed are methods for the preparation of amorphous solid dispersion of N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindo1-2(1H)-yl]-4-(trifluoromethyl)-benzamide.

Claims (13)

1. A method for producing an amorphous solid dispersion of N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl]-4-(trifluoromethyl)-benzamide, said method comprising:

(a) preparing a liquid solution comprising N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl]-4-(trifluoromethyl)-benzamide, at least one polymer and a solvent; and

(b) spray drying said liquid solution, thereby producing said amorphous solid dispersion.

2. The method of claim 1 , wherein said liquid solution comprises at least one solvent selected from the group consisting of tetrahydrofuran, alcohol, ethyl acetate, acetone, methoxy acetone (methyl ether ketone), dichloromethane, and water, or mixtures thereof.

3. The method of claim 2 , wherein said solvent is tetrahydrofuran.

4. The method of claim 2 , wherein said solvent is methanol or acetone.

5. The method of claim 1 , wherein said polymer is selected from the group consisting of methacrylic acid copolymer, Hydroxypropyl methyl cellulose (HPMC), HPMCP-H55, CAP, PVAP, HPMCAS-L, HPMCAS-M, HPMCAS-H, Hypromellose, HPC, Poloxamer, PVP VA, PVP(neutral), hydroxypropyl cellulose, methyl cellulose, and ethyl cellulose, or mixtures thereof.

6. The method of claim 5 , wherein said polymer is (Hydroxypropyl) methyl cellulose acetate succinate (HPMCAS).

7. The method of claim 1 , wherein said liquid solution comprises a surfactant.

8. The method of claim 7 , wherein said surfactant is selected from the group consisting of Polysorbate, and polyoxyethylated triglycerides.

9. The method of claim 1 , wherein the ratio by weight of N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl]-4-(trifluoromethyl)-benzamide to the polymer in said solution is from about 1:50 to about 1:1.

10. The method of claim 1 , wherein the ratio by weight of N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl]-4-(trifluoromethyl)-benzamide to the polymer in said solution is about 1:9.

11. The method of claim 1 , wherein the ratio by weight of N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl]-4-(trifluoromethyl)-benzamide to the polymer in said solution is about 1:2.

Assignments (2)
CHANGE OF ADDRESS Recorded Mar 25, 2026
From: SIGA TECHNOLOGIES, INC.
To: SIGA TECHNOLOGIES, INC.
Reel/Frame 075242/0438 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2017
From: TYAVANAGIMATT, SHANTHAKUMAR R.; SAMUEL, N K PETER; PAZ, JOSEPH; TAN, YING; HRUBY, DENNIS E.
To: SIGA TECHNOLOGIES, INC.
Reel/Frame 042162/0388 →