Stabilized formulations containing anti-PCSK9 antibodies
AssigneeRegeneron Pharmaceuticals, Inc.
InventorsScott M. Walsh, Daniel B. Dix
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AssigneeRegeneron Pharmaceuticals, Inc.
InventorsScott M. Walsh, Daniel B. Dix
Estimating the term…
The present invention provides pharmaceutical formulations comprising a human antibody that specifically binds to human proprotein convertase subtilisin/kexin type 9 (PCSK9). The formulations may contain, in addition to an anti-PCSK9 antibody, at least one amino acid, at least one sugar, or at least one non-ionic surfactant. The pharmaceutical formulations of the present invention exhibit a substantial degree of antibody stability after storage for several months.
A liquid pharmaceutical formulation consisting of:
A liquid pharmaceutical formulation consisting of:
A liquid pharmaceutical formulation consisting of:
Dependencies are inferred from the claim text.
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Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies: against enzymes
Against materials from animals: against proteinaceous materials, e.g. enzymes, hormones, lymphokines
Antibodies ; Immunoglobulins; Immune serum, e.g. antilymphocytic serum: stabilisation, fragmentation
Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite: heterocyclic compounds, e.g.…
About 5 years 9 months of term left · ends 27 Jul 2032 (estimated)
The present invention relates to the field of therapeutic antibody formulations. More specifically, the present invention relates to the field of pharmaceutical formulations comprising a human antibody that specifically binds to human proprotein convertase subtilisin/kexin type 9 (PCSK9).
A Request for Transfer of a Computer Readable Form is filed herewith. The Request transfers the computer readable form filed on Jul. 26, 2012 in U.S. patent application Ser. No. 13/559,862, which was filed on Jul. 27, 2012. A paper copy or PDF of the sequence listing, which is identical in content to the computer readable form, is included as part of the present specification.
Therapeutic macromolecules (e.g., antibodies) must be formulated in a manner that not only makes the molecules suitable for administration to patients, but also maintains their stability during storage and subsequent use. For example, therapeutic antibodies in liquid solution are prone to degradation, aggregation or undesired chemical modifications unless the solution is formulated properly. The stability of an antibody in liquid formulation depends not only on the kinds of excipients used in the formulation, but also on the amounts and proportions of the excipients relative to one another. Furthermore, other considerations aside from stability must be taken into account when preparing a liquid antibody formulation. Examples of such additional considerations include the viscosity of the solution and the concentration of antibody that can be accommodated by a given formulation, and the visual quality or appeal of the formulation. Thus, when formulating a therapeutic antibody, great care must be taken to arrive at a formulation that remains stable, contains an adequate concentration of antibody, and possesses a suitable viscosity as well as other properties which enable the formulation to be conveniently administered to patients.
Before the present invention is described, it is to be understood that this invention is not limited to particular methods and experimental conditions described, as such methods and conditions may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. As used herein, the term “about”, when used in reference to a particular recited numerical value or range of values, means that the value may vary from the recited value by no more than 1%. For example, as used herein, the expression “about 100” includes 99 and 101 and all values in between (e.g., 99.1, 99.2, 99.3, 99.4, etc.).
Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned herein are incorporated herein by reference to describe in their entirety.