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US4812557A Expired / Lapsed US ⏱️ 0.0 years remaining

Stable composition of interleukin-2 and human serum albumin

Assignee: Takeda Pharmaceutical Co Ltd
•
Filing: 1986-11-17
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Granted: 1989-03-14
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Expires: 2006-11-17
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Abstract

Abstract The present invention provides an interleukin-2 composition which comprises human serum albumin, a reducing compound or a combination thereof and is adjusted as showing pH of 3 to 6 as a solution. The composition of the present invention is characterized in that interleukin-2 activity is minimized during storage and in the processes of freezing and lyophilization.

Inventors

  • 👤 Mikura Yasushi
  • 👤 Asada Kensuke
  • 👤 Toguchi Hajime

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 20:17
CPC Classifications
A; A61; A61K; A61K38/00; A61K38/16; A61K47/00; A61K47/30; A61K47/42; A61K38/17; A61K38/19; A61K38/20; A61K38/2013; A61K47/06; A61K47/16; A61K47/18; A61K47/183; A61K9/00; A61K9/0012; A61K9/0019; A61K9/14; A61K9/19; Y; Y10; Y10S; Y10S435/00; Y10S435/8215; Y10S435/948; Y10S530/00; Y10S530/827; Y10S530/828; Y10S930/00; Y10S930/01; Y10S930/14; Y10S930/141

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 51 words
A human interleukin-2 composition in the form of an aqueous solution or frozen matter which comprises in addition to human interleukin-2, human serum albumin in a concentration of about 0.1 to 50 mg/ml as an aqueous solution, and, as a solution, is adjusted to have a pH between 3 to 5.5.
Claim 2
Dependent Claim 51 words
A human interleukin-2 composition in the form of an aqueous solution or frozen matter which comprises in addition to human interleukin-2, human serum albumin in a concentration of about 0.1 to 50 mg/ml as an aqueous solution, and, as a solution, is adjusted to have a pH between 3 to 5.5.
Claim 3
Dependent Claim 15 words
The composition according to claim 1, wherein the human interleukin-2 is a recombinant human interleukin-2.
Claim 4
Dependent Claim 15 words
The composition according to claim 1, wherein the human interleukin-2 is a non-glycosylated human interleukin-2.
Claim 5
Dependent Claim 19 words
The composition according to claim 1, wherein the human interleukin-2 has a specific activity of 20,000 to 80,000 units/mg.
Claim 6
Dependent Claim 23 words
The composition according to claim 1, wherein the human interleukin-2 is in a concentration of 1 to 80,000 units/ml as an aqueous solution.
Claim 7
Dependent Claim 12 words
The composition according to claim 1, which is free from a salt.
Claim 8
Dependent Claim 27 words
The composition according to claim 1, which further comprises a monoamino aliphatic amino acid, a cyclic amino acid, a monosaccharide, a sugar alcohol or a combination thereof.
Claim 9
Dependent Claim 14 words
The composition according to claim 1, which further comprises a monoamino aliphatic amino acid.
Claim 10
Dependent Claim 25 words
The composition according to claim 8, wherein the monoamino aliphatic amino acid is in a concentration of 5 to 50 mg/ml as an aqueous solution.
Claim 11
Dependent Claim 32 words
The composition according to claim 1, wherein the pH of the composition is adjusted by an acidic reducing compound, an acidic amino acid, a mineral acid or/and a buffer of organic acid.
Claim 12
Dependent Claim 28 words
The composition according to claim 7, wherein the additional component is a monosaccharide, a sugar alcohol or a combination thereof in a concentration of 10 to 100 mg/ml.
Claim 13
Dependent Claim 18 words
The composition according to claim 1, comprising a combination of the human serum albumin and a reducing compound.
Claim 14
Dependent Claim 15 words
The composition according to claim 12, wherein the reducing compound is an acidic reducing compound.
Claim 15
Dependent Claim 27 words
The composition according to claim 13, wherein the acidic reducing compound is glutathione, thioctic acid, N-acetylcysteine, thioalkanoic acid of 1 to 7 carbon atoms or ascorbic acid.
Claim 16
Dependent Claim 21 words
The composition according to claim 12, wherein the reducing compound is in a concentration of 0.05-20 mg/ml as an aqueous solution.

References Cited (Backward Citations)

US4508833A Cited
EP0091258A2 Cited
FR2532178A1 Cited
US4490289A Cited
EP0145390A2 Cited
US4530787A Cited
US4569790A Cited
US4604377A Cited
US4530787B1 Cited
US4645830A Cited
US4572798A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1992-03-13 1992-09-12 1993-03-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1996-03-13 1996-09-12 1997-03-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2000-03-13 2000-09-12 2001-03-14 $7700.00 Window Closed / Lapsed

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