US2021284986A1PendingUtilityA1
Lyophilized formulations for factor xa antidote
Est. expiryAug 20, 2034(~8.1 yrs left)· nominal 20-yr term from priority
A61P 7/02A61K 38/48A61K 38/36A61K 9/08A61K 9/0019A61K 47/26C12N 9/6432C07K 14/00C12Y 304/21006A61K 9/19A61K 47/183A61K 38/4846A61K 47/12
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Claims
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
exact text as granted — not AI-modified1 . A lyophilized composition prepared by lyophilizing an aqueous solution comprising from 40 mM to 50 mM arginine, from 1% to 3% sucrose (w/v), from 2% to 8% mannitol (w/v) and 5 to 50 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 aqueous solution has a pH from 7.7 to 7.9.
2 . The lyophilized formulation of claim 1 , wherein the aqueous solution comprises 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 lyophilized formulation of claim 2 , wherein the aqueous solution comprises at least 18 mg/mL of the polypeptide.
4 . The lyophilized formulation of claim 1 , wherein the polypeptide comprises at least an intra-chain disulfide bond for each of the first and second chains.
5 . The lyophilized formulation of claim 1 , wherein the aqueous solution comprises about 45 mM arginine, about 2% sucrose (w/v), about 5% mannitol (w/v) and about 10 mg/mL of the two-chain polypeptide, wherein the aqueous solution has a pH of about 7.8.
6 . The lyophilized formulation of claim 1 , wherein the aqueous solution comprises about 45 mM arginine, about 2% sucrose (w/v), about 5% mannitol (w/v) and about 20 mg/mL of the two-chain polypeptide, wherein the aqueous solution has a pH of about 7.8.
7 . The lyophilized formulation of claim 1 , which comprises L-arginine HCl:sucrose:mannitol in a weight ratio of the range of (0.5-1.4):(1-3):(2-8).
8 . The lyophilized formulation of claim 1 , which comprises L-arginine HCl:sucrose:mannitol in a weight ratio of the range of (0.9-1):(1.5-2.5):(4.5-5.5).
9 . The lyophilized formulation of claim 1 , which comprises L-arginine HCl:sucrose:mannitol in a weight ratio of about 0.95:2:5.
10 . An aqueous solution comprising from 40 mM to 50 mM arginine, from 1% to 3% sucrose (w/v), from 2% to 8% mannitol (w/v) and 5 to 50 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 aqueous solution has a pH from 7.7 to 7.9.
11 . An aqueous solution prepared by dissolving the lyophilized formulation of claim 1 in water.Join the waitlist — get patent alerts
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