Nobivac NXT HCPChFeLV RSS Authorised This medicine is authorised for use in the European Union feline calicivirosis, feline rhinotracheitis, feline panleucopenia, feline chlamydiosis (live) and feline leukemia (self-amplifying RNA particle) vaccineMedicineVeterinaryAuthorised
Page contentsPage contents Overview Product details Authorisation details Assessment history News on Nobivac NXT HCPChFeLV Application under evaluation CVMP opinion European Commission decision OverviewUp-to-date information on this veterinary medicinal product is available on the Veterinary Medicines Information website Product details Name of medicine Nobivac NXT HCPChFeLV Active substance feline herpesvirus 1 (FHV), strain G2620A, livefeline calicivirus (FCV), strain F9, livefeline panleucopenia virus (FPL), strain MW-1chlamydia felis, strain Baker, livefeline leukemia virus (FeLV) self-amplifying RNA (saRNA)-particle International non-proprietary name (INN) or common name feline calicivirosis, feline rhinotracheitis, feline panleucopenia, feline chlamydiosis (live) and feline leukemia (self-amplifying RNA particle) vaccine Pharmacotherapeutic groupImmunologicals for felidaeOther immunologicals Authorisation details EMA product number EMEA/V/C/006520 Assessment history Initial marketing authorisation documents CVMP summary of positive opinion for Nobivac NXT HCPChFeLVAdopted Reference Number: EMA/CVMP/75635/2026 Rev. 1 English (EN) (144.38 KB - PDF)First published: 17/04/2026 Last updated: 19/06/2026 View News on Nobivac NXT HCPChFeLV Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 16-18 June 202619/06/2026 Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 14-16 April 202617/04/2026 EMA recommends authorisation of first veterinary vaccine using RNA technology17/04/2026 This page was last updated on 25/08/2026 Share this page