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Antibody-containing solution pharmaceuticals

Inactive Publication Date: 2005-06-02
CHUGAI PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0009] The object of the present invention is to provide an antibody-containing solution formulation that is stable for long-term storage. This formulation is designed to suppress the formation of visible insoluble matter and / or insoluble particles, which are derived from the aggregation of antibodies caused by physical stresses (e.g., freezing-thawing) during its production process and by long-term storage; and to suppress the formation of visible insoluble matter and / or insoluble particles in the presence of metal ions (Fe ions) introduced during the production process.
[0010] As a result of extensive and intensive efforts made to achieve the above object, the inventors of the present invention have found that the use of organic acids significantly suppresses the formation of visible insoluble matter in the presence of iron, and that the addition of surfactants very significantly suppresses the formation of visible insoluble matter and / or insoluble particles during shaking and freezing-thawing steps. These findings have led to the completion of the present invention.

Problems solved by technology

When proteins are stored in a highly concentrated solution form, they are usually associated with a problem of deterioration, including the formation of insoluble aggregates, which is required to be prevented.
However, the anti-HM1.24 antibody is an unstable protein and is more likely to undergo physical and chemical changes (e.g., association, aggregation) as a result of stresses in the purification process.
However, repeating such shaking and freezing-thawing steps causes the formation of antibody aggregates and / or insoluble particles.
Furthermore, long-term storage causes decomposition of antibodies, resulting in formation of decomposition products.
There is also a problem that visible insoluble matter and insoluble particles are formed in the presence of metal ions (Fe ions) introduced during the production process.
However, there is a limit to removal methods such as precipitation, complex formation, and so on.
However, when added as stabilizers, organism-derived high-molecular weight materials like proteins are disadvantageous in that very complicated processes are required to remove contaminants, such as viruses and prions.

Method used

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  • Antibody-containing solution pharmaceuticals

Examples

Experimental program
Comparison scheme
Effect test

example 1

Effects of Organic Acid Addition

[0087] Anti-HM1.24 antibody formulations prepared in different buffers (phosphate, acetate, citrate) were supplemented with iron (FeCl3), and observed for the formation of visible insoluble matter by the unaided eye against a black background in accordance with the foreign insoluble matter test. The samples were stored at room temperature (about 25° C.). Table 1 summarizes the composition of tested formulations, and Table 2 shows the results obtained.

TABLE 1Composition of tested formulationsSample No.123456789101112Anti-HM1.242.52.52.52.52.52.52.52.52.52.52.52.5antibody(mg / mL)Polysorbate 800.0250.0250.0250.0250.0250.0250.0250.0250.0250.0250.0250.025(%)Buffer typeAcAcAcAcPhosPhosPhosPhosCitCitCitCitBuffer conc.202020202020202020202020(mM)Sodium100100100100100100100100100100100100chloride(mM)pH6.06.06.06.06.06.06.06.06.06.06.06.0FeCl3 conc.010100100001010010000101001000(μg / L)

Ac: acetate buffer,

Phos: phosphate buffer,

Cit: citrate buffer

[0088]

TABLE ...

example 2

Effects of Surfactant Addition

[0090] Polysorbate 80, Polysorbate 20 and Poloxamer 188 were used in the shaking test, freezing-thawing test and storage stability test of anti-HM1.24 antibody formulations (2.5 to 10 mg / mL) to study surfactant-induced effects on the formulations.

(1) Physical Stress Test

[0091] Surfactant-induced effects on physical stresses (shaking and freezing-thawing) were studied in terms of insoluble particle or visible insoluble matter formation.

(1-1) Test on 2.5 mg / mL Solutions

[0092] The evaluation was conducted as follows. Table 3 shows the composition of tested formulations along with the results obtained. [0093] Test sample: 2 mL per 5 mL vial (Samples 13-22) [0094] Evaluation: insoluble particle test using a light shielding type of an automatic particle analyzer (HIAC) [0095] Evaluation conditions:

(i) Shaking Test [0096] Shaking conditions: 200 strokes / min.×30 min. [0097] Shaker: RECIPRO SHAKER SR-I [0098] (Taiyo Scientific Industrial Co., Ltd.)

(ii...

example 3

Dependency on pH

[0121] To confirm the optimum pH for the anti-HM1.24 antibody in the concentration range of 2.5 to 10 mg / mL, the heat resistance test and the storage stability test were conducted.

(1) Test on 2.5 mg / mL Formulations

[0122] The evaluation was conducted as follows. Tables 7 and 8 show the composition of tested formulations and the results obtained, respectively. [0123] Test sample: 1 mL per 5 mL vial (Samples 43-47) [0124] Evaluation: heat resistance test, storage stability test [0125] Storage conditions: [0126] at 50° C. for 3 moths (50° C.-3M)(GPC)

[0127] at 5° C. for 6 months (5° C.-6M)(IEC)

TABLE 7Composition of tested formulationsSample No.4344454647Anti-HM1.24 antibody2.52.52.52.52.5(mg / mL)Acetate buffer (mM)2020202020Sodium chloride (mM)100100100100100Polysorbate 80 (%)0.0250.0250.0250.0250.025PH5.05.56.06.57.0

[0128]

TABLE 8Evaluation results of heat resistance test (50° C.-3M) andstorage stability test (5° C.-6M)GPC (50° C.-3M)SampleResidueAggregationDecompos...

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Abstract

An antibody-containing solution formulation comprising an organic acid and a surfactant as stabilizers; a method for suppressing the formation of visible insoluble matter and / or insoluble particles due to the presence of metal ions in an antibody-containing solution formulation, which comprises adding an organic acid to the solution; a method for suppressing the formation of visible insoluble matter and / or insoluble particles during shaking and freezing-thawing of an antibody-containing solution, which comprises adding a surfactant to the solution; and a method for stabilizing an antibody-containing solution, which comprises adding an organic acid and a surfactant.

Description

TECHNICAL FIELD [0001] The present invention relates to stable solution formulations containing antibodies. BACKGROUND ART [0002] Advances in gene recombination technology have enabled the pharmaceutical use of antibodies such as immunoglobulins, monoclonal antibodies and humanized antibodies. To ensure a stable supply of these antibodies, it is necessary to establish production and storage conditions where the structure and activity of the antibodies can be maintained. [0003] When proteins are stored in a highly concentrated solution form, they are usually associated with a problem of deterioration, including the formation of insoluble aggregates, which is required to be prevented. It is necessary to prevent such deterioration. For example, the applicant has found that an anti-HM1.24 antibody has a therapeutic effect on myeloma cells (JP KOKAI 11-092399), and also has studied formulation of this antibody. However, the anti-HM1.24 antibody is an unstable protein and is more likely t...

Claims

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Application Information

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IPC IPC(8): A61K9/08A61K9/00A61K39/395A61K47/04A61K47/10A61K47/12A61K47/14A61K47/26C07K16/30C07K16/40C07K16/44
CPCA61K9/0019C07K16/3061A61K39/39591A61K47/10A61K2039/505A61K47/12C07K16/44A61K47/26C07K16/40C07K16/00A61P37/04A61K47/34A61K39/395A61K9/08
Inventor MIZUSHIMA, HIDEFUMIMIYAUCHI, EIICHI
Owner CHUGAI PHARMA CO LTD
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