IP Library Granted Patent US 9,663,563
Granted Patent B2
US 9,663,563 · App. 14/204,618 · Granted May 30, 2017

Aqueous liquid composition

Inventors: Tomomi Nakatani (Ibaraki, JP); Koichi Saito (Ibaraki, JP)
Assignee: Sumitomo Dainippon Pharma Co., Ltd.
C07K14/4748A61K9/0019A61K39/0011A61K47/12A23V2200/308A61K9/08A61K38/00C07K7/00
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Quick Facts
Patent No.
US 9,663,563
App. No.
14/204,618
Granted
May 30, 2017
Kind
B2
Abstract

The invention provides an aqueous liquid composition comprising a WT1 protein-derived cancer antigen peptide, wherein the peptide is stabilized. The aqueous liquid composition contains a peptide and an excipient, and has a pH of 3-6. The peptide has the amino acid sequence Arg-Met-Phe-Pro-Asn-Ala-Pro-Tyr-Leu (SEQ ID NO: 1), wherein optionally 1 to 3 amino acids are deleted, substituted and/or added, such that the peptide has a cytotoxic T cell-inducing ability. The excipient is (a) an alpha hydroxyl acid selected from glycolic acid, lactic acid, malic acid, tartaric acid, citric acid and pharmacologically acceptable salts thereof, (b) a dicarboxylic acid selected from malonic acid, succinic acid, glutaric acid, maleic acid and pharmacologically acceptable salts thereof, and/or (c) methionine.

Claims (27)

1. An aqueous liquid composition consisting essentially of a peptide and an excipient, and having a pH of 3-6:

wherein the peptide is selected from the group consisting of the amino acid sequences of SEQ ID NOs: 1-7, and

wherein the excipient consists of one or more kinds selected from the group consisting of the following (C), (D) and (E),

(C) one or more kinds of alpha hydroxy acids selected from the group consisting of glycolic acid, lactic acid, malic acid, tartaric acid, citric acid and pharmacologically acceptable salts thereof,

(D) one or more kinds of dicarboxylic acids selected from the group consisting of malonic acid, succinic acid, glutaric acid, maleic acid and pharmacologically acceptable salts thereof, and

(E) methionine.

2. The aqueous liquid composition according to claim 1 , wherein the peptide consists of the amino acid sequence Arg-Met-Phe-Pro-Asn-Ala-Pro-Tyr-Leu (SEQ ID NO: 1).

3. The aqueous liquid composition according to claim 1 , wherein the excipient consists of both (C) and (E).

4. The aqueous liquid composition according to claim 1 , wherein the excipient consists of both (C) and (E), and (C) is one or more kinds of alpha hydroxy acids selected from the group consisting of glycolic acid, lactic acid, malic acid, tartaric acid and pharmacologically acceptable salts thereof.

5. The aqueous liquid composition according to claim 1 , wherein the excipient consists of both (D) and (E).

6. The aqueous liquid composition according to claim 1 , wherein the excipient consists of both (D) and (E), and (D) is one or more kinds of dicarboxylic acids selected from the group consisting of succinic acid and a pharmacologically acceptable salt thereof.

7. The aqueous liquid composition according to claim 1 , wherein the content per volume of alpha hydroxy acid is 1-100 mM or the content per volume of dicarboxylic acid is 10-100 mM.

8. The aqueous liquid composition according to claim 1 , wherein the content per volume of methionine is 1-300 mM.

9. A method of improving stability of a peptide, consisting of the amino acid sequence shown by Arg-Met-Phe-Pro-Asn-Ala-Pro-Tyr-Leu (SEQ ID NO: 1), in an aqueous liquid composition by adding an excipient:

wherein

the excipient consists of one or more kinds selected from the group consisting of the following (C), (D) and (E)

(C) one or more kinds of alpha hydroxy acids selected from the group consisting of glycolic acid, lactic acid, malic acid, tartaric acid, citric acid and pharmacologically acceptable salts thereof,

(D) one or more kinds of dicarboxylic acids selected from the group consisting of malonic acid, succinic acid, glutaric acid, maleic acid and pharmacologically acceptable salts thereof, and

(E) methionine, and wherein the aqueous liquid composition after addition of the excipient has a pH of 3-6.

10. The aqueous liquid composition according to claim 2 , wherein the excipient consists of both (C) and (E).

11. The aqueous liquid composition according to claim 2 , wherein the excipient consists of both (C) and (E), and (C) is one or more kinds of alpha hydroxy acids selected from the group consisting of glycolic acid, lactic acid, malic acid, tartaric acid and pharmacologically acceptable salts thereof.

12. The aqueous liquid composition according to claim 11 , wherein the content per volume of alpha hydroxy acid is 1-100 mM.

13. The aqueous liquid composition according to claim 11 , wherein the content per volume of methionine is 1-300 mM.

14. The aqueous liquid composition according to claim 2 , wherein the excipient consists of both (D) and (E).

15. The aqueous liquid composition according to claim 2 , wherein the excipient consists of both (D) and (E), and (D) is one or more kinds of dicarboxylic acids selected from the group consisting of succinic acid and a pharmacologically acceptable salt thereof.

16. The aqueous liquid composition according to claim 15 , wherein the content per volume of dicarboxylic acid is 10-100 mM.

17. The aqueous liquid composition according to claim 15 , wherein the content per volume of methionine is 1-300 mM.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2020
From: SUMITOMO DAINIPPON PHARMA CO., LTD.
To: INTERNATIONAL INSTITUTE OF CANCER IMMUNOLOGY, INC.
Reel/Frame 054751/0803 →
CHANGE OF NAME Recorded Aug 25, 2014
From: DAINIPPON SUMITOMO PHARMA CO., LTD.
To: SUMITOMO DAINIPPON PHARMA CO., LTD.
Reel/Frame 033606/0307 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 30, 2014
From: NAKATANI, TOMOMI; SAITO, KOICHI
To: DAINIPPON SUMITOMO PHARMA CO., LTD.
Reel/Frame 032999/0480 →
Continuity (2)
Provisional Application 61777423 · Mar 12, 2013
Related Publication 20140271693A1 · Sep 18, 2014