FIELD: biochemistry.
SUBSTANCE: group of inventions relates to biochemistry. Aqueous composition having an inhibitory effect on TNF (variants) is proposed. In a first embodiment, the aqueous composition comprises an isolated polypeptide, a salt in a concentration of 80 to 130 mM, an aqueous buffer at a concentration of 20–30 mM, and sucrose at a concentration of 34–80 mg/ml. In this composition, arginine and cysteine are not presented. In a second embodiment, the aqueous composition comprises an isolated polypeptide, a salt in a concentration of 80 to 130 mM, wherein the salt is not present at a concentration of 100 mM, a succinate buffer selected from trehalose and sucrose, or a combination thereof. No free amino acids are present in said composition. Isolated polypeptide in each composition is an extracellular ligand-binding part of the human p75 tumor necrosis factor receptor fused to the human IgG1 Fc domain.
EFFECT: invention provides an aqueous composition having high stability at high temperatures without arginine and cysteine.
41 cl, 15 dwg
Title | Year | Author | Number |
---|---|---|---|
PHARMACEUTICAL COMPOSITIONS OF SAPOSIN C AND METHODS FOR TREATING CANCER | 2018 |
|
RU2767199C1 |
LIQUID COMPOSITION OF POLYPEPTIDES CONTAINING FC DOMAIN OF IMMUNOGLOBULIN | 2011 |
|
RU2600847C2 |
STABLE PHARMACEUTICAL COMPOSITION | 2017 |
|
RU2736830C2 |
STABLE COMPOSITIONS WITH HIGH CONCENTRATIONS OF PROTEINS OF HUMAN ANTIBODIES AGAINST TNF-ALPHA | 2010 |
|
RU2560701C2 |
STABLE COMPOSITIONS OF IMMUNOGLOBULIN SINGLE VARIABLE DOMAIN AND THEIR USE | 2014 |
|
RU2773172C2 |
PHARMACEUTICAL COMPOSITION CONTAINING ADALIMUMAB | 2014 |
|
RU2664736C2 |
METHODS AND COMPOSITIONS FOR CNS DELIVERY OF ARYLSULFATASE A | 2011 |
|
RU2671503C2 |
METHODS AND COMPOSITIONS FOR DELIVERY OF ARYLSULFATASE A TO CNS | 2011 |
|
RU2783380C2 |
PHARMACEUTICAL FORMULA CONTAINING HUMAN ANTI-TSLP ANTIBODY | 2016 |
|
RU2794148C2 |
STABLE FORMULATIONS OF IMMUNOGLOBULIN SINGLE VARIABLE DOMAIN AND USE THEREOF | 2014 |
|
RU2671977C2 |
Authors
Dates
2018-08-08—Published
2014-04-29—Filed