IP Library Patent Application 15136810
Patent Application
App. No. 15/136,810

LYOPHILIZED FORMULATIONS FOR FACTOR XA ANTIDOTE

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Patent No.
US None
App. No.
15/136,810
Abstract

The present disclosure relates to solutions and methods of preparing lyophilized formulations of factor Xa (fXa) antidotes. A suitable aqueous formulation suitable for lyophilization can include a fXa antidote, a solubilizing agent, a stabilizer, and a crystalline component, wherein the formulation does not collapse during lyophilization.

Claims (21)

1 . An aqueous formulation, comprising from 10 mM to 55 mM arginine, from 1% to 3% sucrose (w/v), from 2% to 8% mannitol (w/v) and at least 5 mg/mL of a two-chain polypeptide comprising a first chain comprising the amino acid sequence of SEQ ID NO. 4, a second chain comprising the amino acid sequence of SEQ ID NO. 5, and a disulfide bond between a first Cysteine residue at position 98 (Cys98) of SEQ ID NO. 4 and a second Cysteine residue at position 108 (Cys108) of SEQ ID NO. 5, wherein the formulation has a pH from 7.5 to 8.

2 . The formulation of claim 1 , comprising from 40 mM to 50 mM arginine, from 1.5% to 2.5% sucrose (w/v), from 4.5% to 5.5% mannitol (w/v) and at least 10 mg/mL of the polypeptide.

3 . The formulation of claim 2 , comprising at least 18 mg/mL of the polypeptide.

4 . The formulation of claim 2 , wherein the polypeptide comprises an amino acid residue that is modified to be different from natural amino acids.

5 . The formulation of claim 4 , wherein residue Asp29 of the first chain is modified to (3R)-3-hydroxyAsp at Asp29.

6 . The formulation of claim 1 , wherein the polypeptide comprises at least an intra-chain disulfide bond for each of the first and second chains.

7 . The formulation of claim 1 , comprising at least about 10 mg/mL of the two-chain polypeptide.

8 . The formulation of claim 1 , comprising at least about 20 mg/mL of the two-chain polypeptide.

9 . An aqueous formulation, comprising from 10 mM to 55 mM arginine, from 1% to 3% sucrose (w/v), from 2% to 8% mannitol (w/v) and at least 5 mg/mL of a two-chain polypeptide comprising a first chain comprising the amino acid sequence of SEQ ID NO. 4 or having at least 90% sequence identity to SEQ ID NO. 4, a second chain of the amino acid sequence of SEQ ID NO. 5 or having at least 90% sequence identity to SEQ ID NO. 5, and a disulfide bond between a first Cysteine residue at position 98 (Cys98) of SEQ ID NO. 4 and a second Cysteine residue at position 108 (Cys108) of SEQ ID NO. 5, wherein the formulation has a pH from 7.5 to 8.

10 . The formulation of claim 9 , wherein the two-chain polypeptide has modifications to the Gla domain and the active site as compared to the wild-type fXa protein, is able to bind to a fXa inhibitor but does not assemble into a prothrombinase complex.

11 . A method of preparing a lyophilized formulation, comprising lyophilizing the aqueous formulation of claim 1 .

12 . A lyophilized composition obtainable by lyophilizing the aqueous formulation of claim 1 .

13 . A lyophilized composition comprising at least 10% (w/w) of a two-chain polypeptide comprising a first chain of the amino acid sequence of SEQ ID NO. 4, a second chain of the amino acid sequence of SEQ ID NO. 5, and a disulfide bond between a first Cysteine residue at position 98 (Cys98) of SEQ ID NO. 4 and a second Cysteine residue at position 108 (Cys108) of SEQ ID NO. 5, and L-arginine HCl:sucrose:mannitol in a weight ratio of the range (0.5-1.4):(1-3):(2-8).

14 . The lyophilized composition of claim 13 , comprising at least 18% (w/w) of the two-chain polypeptide.

15 . The lyophilized composition of claim 13 , wherein the weight ratio of L-arginine HCl:sucrose:mannitol is in the range of (0.9-1):(1.5-2.5):(4.5-5.5).

16 . The lyophilized composition of claim 13 , wherein the weight ratio of L-arginine HCl:sucrose:mannitol is about 0.95:2:5.

17 . A method of reducing bleeding in a subject undergoing anticoagulant therapy with a factor Xa inhibitor comprising administering to the subject a solution prepared by dissolving the lyophilized composition of claim 13 in an aqueous solvent.

18 . The method of claim 17 , wherein the factor Xa inhibitor is apixaban, rivaroxaban or betrixaban.

19 . An aqueous formulation, comprising a polypeptide comprising the amino acid sequence of SEQ ID NO. 3 or an amino acid sequence having at least 95% sequence identity to SEQ ID NO. 3, a solubilizing agent, a stabilizer, and a crystalline component, wherein the formulation does not collapse during lyophilization.

20 . The formulation of claim 19 , wherein the crystalline component is mannitol present in a concentration from 2% to 8% (w/v), the solubilizing agent is arginine and the stabilizer is sucrose.

21 . The formulation of claim 19 , further comprising a surfactant and a buffer.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2022
From: ALEXION PHARMACEUTICALS, INC.
To: ALEXION PHARMA INTERNATIONAL OPERATIONS UNLIMITED COMPANY
Reel/Frame 060799/0729 →
CHANGE OF NAME Recorded Jan 7, 2021
From: PORTOLA PHARMACEUTICALS, INC.
To: PORTOLA PHARMACEUTICALS, LLC
Reel/Frame 054920/0739 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2021
From: PORTOLA PHARMACEUTICALS, LLC
To: ALEXION PHARMACEUTICALS, INC.
Reel/Frame 054921/0131 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2021
From: ALEXION PHARMA INTERNATIONAL OPERATIONS UNLIMITED COMPANY
To: ALEXION PHARMACEUTICALS, INC.
Reel/Frame 054922/0857 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2016
From: WANG, JUAN; SACHA, GREGORY A.; NGUYEN, PHUONG M.
To: PORTOLA PHARMACEUTICALS, INC.
Reel/Frame 038619/0958 →