Highly concentrated pharmaceutical formulations
AssigneeGenentech, Inc.
InventorsMichael Adler, Hanns-Christian Mahler, Oliver Boris Stauch
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AssigneeGenentech, Inc.
InventorsMichael Adler, Hanns-Christian Mahler, Oliver Boris Stauch
Estimating the term…
The present invention relates to a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-CD20 antibody, such as e.g. Rituximab, Ocrelizumab, or HuMab<CD20>, or a mixture of such antibody molecules for subcutaneous injection. In particular, the present invention relates to formulations comprising, in addition to a suitable amount of the anti-CD20 antibody, an effective amount of at least one hyaluronidase enzyme as a combined formulation or for use in form of a co-formulation. The said formulations comprise additionally at least one buffering agent, such as e.g. a histidine buffer, a stabilizer or a mixture of two or more stabilizers (e.g. a saccharide, such as e.g. α,α-trehalose dihydrate or sucrose, and optionally methionine as a second stabilizer), a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. Methods for preparing such formulations and their uses thereof are also provided.
A method of treating non-Hodgkin's lymphoma (NHL) in a human patient comprising administering a formulation comprising Rituximab subcutaneously to the patient, wherein the Rituximab is administered at a fixed dose of 1400 mg thereof.
A method of treating non-Hodgkin's lymphoma (NHL) in a human patient comprising administering a formulation comprising from 100 to 150 mg/ml Rituximab subcutaneously to the patient, wherein the Rituximab is administered at a fixed dose of 1400 mg thereof, and further comprising administering recombinant human PH20 (rHuPH20) to the patient to increase dispersion and absorption of the Rituximab.
Dependencies are inferred from the claim text.