Abstract: An improved method for the manufacture of an oil-in-water emulsion involves three procedures: (i) preparation of a preliminary emulsion; (ii) microfluidization of the preliminary emulsion to reduce its droplet size; and (iii) filtration of the microfluidized emulsion through a hydrophilic membrane. The emulsions are useful as vaccine adjuvants.
Type:
Application
Filed:
December 3, 2010
Publication date:
July 7, 2011
Applicant:
Novartis Vaccines and Diagnostic, GmbH & Co. KG
Abstract: An improved method for the manufacture of an oil-in-water emulsion involves three procedures: (i) preparation of a preliminary emulsion; (ii) microfluidization of the preliminary emulsion to reduce its droplet size; and (iii) filtration of the microfluidized emulsion through a hydrophilic membrane.
Type:
Application
Filed:
December 3, 2010
Publication date:
July 7, 2011
Applicant:
Novartis Vaccines and Diagnostics, GmbH & Co. KG
Inventors:
Harald Rueckl, Hanno Scheffczik, Barbara Santry
Abstract: An improved method for the manufacture of an oil-in-water emulsion involves three procedures: (i) preparation of a preliminary emulsion; (ii) microfluidization of the preliminary emulsion to reduce its droplet size; and (iii) filtration of the microfluidized emulsion through a hydrophilic membrane.
Type:
Application
Filed:
December 3, 2010
Publication date:
July 7, 2011
Applicant:
Novartis Vaccines and Diagnostics, GmbH & Co. KG
Abstract: An immunogenic composition comprising influenza virus haemagglutinin and matrix proteins. These may be from influenza viruses grown in cell culture rather than eggs. The matrix protein may be a fragment of a full-length viral matrix protein e.g. a matrix M1 fragment with a molecular weight of less than 2 OkDa. The composition may be a subunit vaccine comprising purified surface glycoproteins.
Type:
Application
Filed:
January 26, 2007
Publication date:
February 3, 2011
Applicant:
NOVARTIS VACCINES AND DIAGNOSTICS GMBH & CO. KG
Abstract: An influenza vaccine that lacks at least three of a mercurial preservative; an antibiotic; formaldehyde; and egg-derived materials. In some embodiments, the vaccine includes none of these four components.
Type:
Application
Filed:
June 27, 2008
Publication date:
July 22, 2010
Applicant:
Novartis Vaccines & Diagnostics GmbH & Co., KG
Abstract: The present invention relates to vaccine products for the treatment or prevention of viral infections. Further provided are methods of reducing contaminants associated with the preparation of cell culture vaccines. Residual functional cell culture DNA is degraded by treatment with a DNA alkylating agent, such as ?-propiolactone (BPL), thereby providing a vaccine comprising immunogenic proteins derived from a virus propagated on cell culture, substantially free of residual functional cell culture DNA.
Type:
Application
Filed:
November 1, 2006
Publication date:
December 10, 2009
Applicant:
NOVARTIS VACCINES AND DIAGNOSTICS GMBH & CO KG
Abstract: Animal cells are described which can be infected by influenza viruses and which are adapted to growth in suspension in serum-free medium. Processes for the replication of influenza viruses in cell culture using these cells are furthermore described, as well as vaccines which contain the influenza viruses obtainable by the process or constituents thereof.
Type:
Application
Filed:
June 26, 2008
Publication date:
November 6, 2008
Applicant:
NOVARTIS VACCINES AND DIAGNOSTICS GMBH & CO KG