IP Library Granted Patent US 11,096,907
Granted Patent B2
US 11,096,907 · App. 16/043,830 · Granted Aug 24, 2021

Phytonadione compositions and related methods

Inventors: Phanesh Koneru (Lenoir, NC); Sreerarama Murthy Mallipeddi (Lenoir, NC); Jonathan E. Sterling (Lenoir, NC)
Assignee: Exela Holdings, Inc.
A61K31/122A61K9/0019A61K9/107A61K47/26
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Quick Facts
Patent No.
US 11,096,907
App. No.
16/043,830
Granted
Aug 24, 2021
Kind
B2
Abstract

Stable Phytonadione compositions for parenteral administration are provided which comprise (E) isomer of phytonadione at or greater than 97% w/w as the active ingredient, and is substantially free of (Z) isomer. Said compositions are stable, sterile, and particulate-free. Further, said compositions reduce or avoid allergic reactions to benzyl alcohol and polysorbate. In some aspects, the compositions are free or substantially free of benzyl alcohol and/or reduced amounts of polysorbate. Methods of manufacture and methods of administration also provided.

Claims (20)

1. A pharmaceutical composition comprising: Phytonadione in its (E) isomer form at a concentration of from about 0.1 mg/ml to about 20 mg/ml; and optionally a pH adjuster, wherein the composition has a pH of from about 3.5 to about 8.0, wherein Phytonadione (Z) isomer is present in said composition at about 3% w/w or less of the (E) isomer; and wherein said composition is free of benzyl alcohol and, optionally, comprises a polysorbate at a concentration of less than about 1:10 ratio of (E) isomer of phytonadione:polysorbate.

2. The composition of claim 1 , wherein the composition is free of preservatives, antioxidants, and chelating agents.

3. The composition of claim 1 , wherein said composition is in dosage form at a concentration of 2 mg/mL.

4. The composition of claim 3 , wherein the Z-isomer is less than about 3.0% of the composition.

5. The composition of claim 3 , wherein the E-isomer is from about 1.5 to about 5.0 mg/mL.

6. The composition of claim 3 , wherein the E-isomer is exactly or about 1.5 mg/mL; 1.6 mg/mL; 1.7 mg/mL; 1.8 mg/mL; 1.9 mg/mL; 2.0 mg/mL; 2.1 mg/mL; 2.3 mg/mL; 2.5 mg/mL; 2.8 mg/mL; 3.0 mg/mL; 3.3 mg/mL; 3.5 mg/mL; 4.0 mg/mL; 4.5 mg/mL; 5.0 mg/mL; 5.5 mg/mL; 6.0 mg/mL; 7.0 mg/mL; 7.5 mg/mL; 8.0 mg/mL; 8.5 mg/mL; 9.0 mg/mL; 9.5 mg/mL; 10.0 mg/mL; 10.5 mg/mL; 11.0 mg/mL; 12.0 mg/mL; 12.5 mg/mL; or 15.0 mg/mL.

7. The composition of claim 1 , wherein said composition is provided in a non-reacting glass or non-reacting polymeric container selected from a vial container or a pre-filled syringe container.

8. The composition of claim 7 , wherein the container is made of polyethylene or polypropylene or a combination thereof.

9. The composition of claim 1 , wherein said Phytonadione in its (E) isomer form is at a concentration of from about 1.0 mg/mL to about 3.0 mg/mL.

10. The composition of claim 1 , wherein said composition comprises said pH adjuster.

11. The composition of claim 1 , wherein said composition comprises said polysorbate.

12. A method comprising:

administering the composition of claim 1 to a mammal.

13. The method of claim 12 , wherein the mammal is a human.

14. The method of claim 12 , wherein the composition is administered from a vial or a pre-filled syringe wherein the vial or pre-filled syringe is selected from a non-reacting glass or polymeric material.

15. The method of claim 12 , wherein the composition is administered intramuscularly.

16. The method of claim 12 , wherein the composition is administered subcutaneously.

17. A method of manufacturing the composition of claim 7 , comprising: filling said container under vacuum or under an inert gas atmosphere.

18. The method of claim 17 , wherein said container, after filling, has less than 5% of headspace oxygen.

19. The method of claim 17 , wherein said composition in said container has dissolved oxygen of less than or about 1.0 ppm.

Assignments (4)
SECURITY INTEREST Recorded Jun 30, 2021
From: EXELA HOLDINGS, INC.; EXELA PHARMA SCIENCES, LLC; EXELA PHARMSCI, INC.; EXELA STERILE MEDICINES LLC; EXELA STERILE PRODUCTS LLC; EXELA STERILE EQUIPMENT, LLC; EXELA ADVANCED STRATEGIES LLC; AGELEX, LLC; EXELA HEALTH SYSTEMS, LLC; EXELA INITIATIVES, LLC; EXELA INNOVATIONS, LLC
To: LIVE OAK BANKING COMPANY
Reel/Frame 056722/0188 →
SECURITY INTEREST Recorded Jun 30, 2021
From: EXELA HOLDINGS, INC.; EXELA PHARMA SCIENCES, LLC; EXELA PHARMSCI, INC.; EXELA STERILE MEDICINES LLC; EXELA STERILE PRODUCTS LLC; EXELA STERILE EQUIPMENT, LLC; EXELA ADVANCED STRATEGIES LLC; AGELEX, LLC; EXELA HEALTH SYSTEMS, LLC; EXELA INITIATIVES, LLC; EXELA INNOVATIONS, LLC
To: LIVE OAK BANKING COMPANY
Reel/Frame 056722/0250 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2021
From: KONERU, PHANESH; MALLIPEDDI, SREERARAMA MURTHY; STERLING, JONATHAN E.
To: EXELA HOLDINGS, INC.
Reel/Frame 056146/0508 →
SECURITY INTEREST Recorded Oct 1, 2019
From: EXELA HOLDINGS, INC.
To: DEERFIELD PRIVATE DESIGN FUND IV, L.P., AS COLLATERAL AGENT
Reel/Frame 050581/0200 →
Continuity (3)
Continuation In Part 15054797 · Feb 26, 2016
Provisional Application 62121869 · Feb 27, 2015
Related Publication 20190015356A1 · Jan 17, 2019