Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics

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Expired

This medicine's authorisation has expired

prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted)
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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

The marketing authorisation for Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostic expired on 28 November 2015 following the decision of the marketing authorisation holder, Novartis Vaccines and Diagnostics S.r.l., not to apply for a renewal of the marketing authorisation. 

The vaccine contained haemagglutinin and neuraminidase of influenza virus H5N1 A/Vietnam/1194/2004. Novartis Vaccines and Diagnostics S.r.l. (now named Seqirus) confirmed that it did not apply for renewal of the authorisation due to lack of demand for this product. 

Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostic was granted marketing authorisation in the European Union (EU) on 29 November 2010 for immunisation against the H5N1 subtype of influenza A virus. The marketing authorisation was valid for a 5-year period. 

Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostic was a duplicate application to Aflunov, which is authorised in the EU. The marketing authorisation holder (Seqirus) will maintain the marketing authorisation for Aflunov. 

The European Public Assessment Report (EPAR) for Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostic is updated accordingly to reflect the fact that the marketing authorisation is no longer valid.

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Product information

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Latest procedure affecting product information:PSUSA/10008
28/07/2015
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This medicine’s product information is available in all official EU languages.
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Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

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Product details

Name of medicine
Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics
Active substance
influenza virus surface antigens (haemagglutinin and neuraminidase) of strain A/Viet Nam/1194/2004 (H5N1)
International non-proprietary name (INN) or common name
prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted)
Therapeutic area (MeSH)
  • Influenza, Human
  • Immunization
  • Disease Outbreaks
Anatomical therapeutic chemical (ATC) code
J07BB02

Pharmacotherapeutic group

Vaccines

Therapeutic indication

Active immunisation against H5N1 subtype of Influenza A virus.

This indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing A/Vietnam/1194/2004 (H5N1)-like strain.

Prepandemic influenza vaccine (H5N1) Novartis Vaccines and Diagnostic should be used in accordance with official recommendations.

Authorisation details

EMA product number
EMEA/H/C/002269
Marketing authorisation holder
Novartis Vaccines and Diagnostics S.r.l.

Via Fiorentina, 1
IT-53100 Siena
Italy

Marketing authorisation issued
29/11/2010
Expiry of marketing authorisation
28/11/2015
Revision
2

Assessment history

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