IP Library Patent Application 16940885
Patent Application
App. No. 16/940,885

STABILIZED FACTOR IX FORMULATIONS CONTAINING TREHALOSE

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Patent No.
US None
App. No.
16/940,885
Abstract

Methods of preparing lyophilized preparations of Factor IX which preserve more than 90% of the calcium binding property of Factor IX are disclosed. Factor IX formulated with trehalose shows a superior stability profile after 12 weeks storage at 25° C./60% relative humidity (RH) and 40° C./75% RH relative to Factor IX formulated without trehalose. The data suggest that the inclusion of trehalose in the formulation could allow for temperature excursions or even long-term room temperature storage of a Factor IX lyophilized product. The formulations tested contained 10 mM histidine pH 6.8, 3% mannitol, 66 mM sodium chloride, 0.0075% Polysorbate 80, with and without 1% trehalose. Upon storage at 40° C./75% RH or 25° C./60% RH over 12 weeks the trehalose-containing formulation was comparable to product stored at 2-8° C. while the formulation without trehalose was found to undergo significant aggregation and loss of activity. The two formulations demonstrated comparable stability over 26 weeks of real time storage at −20° C. and 2-8° C.

Claims (25)

1 . A lyophilized composition, comprising Factor IX and trehalose, wherein the trehalose is present in an amount sufficient to preserve more than 90% of the calcium binding property of Factor IX during lyophilization and storage for 6 months at 25° C.

2 . The composition of claim 1 , wherein trehalose is present in an amount from 0.5 to 3% by volume.

3 . The composition of claim 2 , wherein trehalose is present in an amount from 1 to 2% by volume.

4 . The composition of claim 1 , further comprising histidine as a buffering agent.

5 . The composition of claim 1 , further comprising mannitol.

6 . The composition of claim 1 , further comprising sodium chloride.

7 . The composition of claim 1 , further comprising polysorbate 80.

8 . The composition of claim 1 , further comprising histidine at a concentration of 5 to 20 mM, mannitol at a concentration of 2 to 5% by volume, sodium chloride at a concentration of 50 to 80 mM, and polysorbate 80 at a concentration of 0.001 to 0.005% by volume.

9 . A method for preparing a stable dried composition of Factor IX, comprising: mixing a solution comprising Factor IX with trehalose to obtain a cryoprotective solution; and freeze drying the cryoprotective solution to obtain a stable dried composition of Factor IX wherein the dried composition of Factor IX retains more than 90% calcium binding activity when stored for 6 months at 25° C.

10 . The method of claim 9 , wherein trehalose is present in an amount from 0.5 to 3% by volume.

11 . The method of claim 10 , wherein trehalose is present in an amount from 1 to 2% by volume.

12 . The method of claim 9 , wherein the solution further comprises histidine.

13 . The method of claim 9 , wherein the solution further comprises mannitol.

14 . The method of claim 9 , wherein the solution further comprises sodium chloride.

15 . The method of claim 9 , wherein the solution further comprises polysorbate 80.

16 . The method of claim 9 , wherein the solution further comprises histidine at a concentration of 5 to 20 mM, mannitol at a concentration of 2 to 5% by volume, sodium chloride at a concentration of 50 to 80 mM, and polysorbate 80 at a concentration of 0.001 to 0.005% by volume.

17 . The method of claim 9 , wherein the freeze drying comprises one annealing step.

18 . A method of lyophilizing a pharmaceutical formulation comprising Factor IX and trehalose comprising the steps of:

(a) freezing the pharmaceutical formulation comprising Factor IX and trehalose at a temperature of −40° C. or less;

(b) annealing the pharmaceutical formulation at between about −20° C. and −35° C.;

(c) lowering the temperature of the pharmaceutical formulation to −40° C. or less;

(d) drying the pharmaceutical formulation in a first drying step at 5° C. to 20° C.

at reduced pressure; and

(e) drying the pharmaceutical formulation in a second drying step at 45° C. to 55° C. at reduced pressure.

19 . The method of claim 18 , wherein the pharmaceutical formulation further comprises histidine at a concentration of 5 to 20 mM, mannitol at a concentration of 2 to 5% by volume, sodium chloride at a concentration of 50 to 80 mM, and polysorbate 80 at a concentration of 0.001 to 0.005% by volume.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Nov 19, 2025
From: BANK OF MONTREAL
To: APTEVO BIOTHERAPEUTICS LLC; MEDEXUS PHARMACEUTICALS, INC.; MEDEXUS PHARMA, INC.
Reel/Frame 072955/0496 →
SECURITY AGREEMENT Recorded Mar 8, 2023
From: APTEVO BIOTHERAPEUTICS LLC
To: BANK OF MONTREAL, AS ADMINISTRATIVE AGENT
Reel/Frame 062992/0829 →