Overview

Leucogen is a veterinary vaccine used in cats from eight weeks of age to protect them against feline leukaemia. Feline leukaemia is an infectious disease of cats which affects the immune system and is caused by the feline leukaemia virus (FeLV). Signs of the disease can include loss of appetite, weight loss, poor fur condition, fever, pale gums and diarrhoea; cats persistently infected with the virus may spread it to other cats. The vaccine is used to prevent the disease signs and persistent viraemia (the presence of FeLV in the blood).

The medicine contains a protein from the outer layer of FeLV.

Leucogen is available as a suspension for injection and can only be obtained with a prescription.

The vaccine is given to cats as an injection under the skin. The initial vaccination course is two injections 3 or 4 weeks apart from 8 weeks of age. In cases where the kitten may have antibodies passed from the mother, a third injection can be given from 15 weeks of age. A booster vaccination of a single injection is necessary one year after the initial vaccination course. Protection starts 3 weeks after the primary course of vaccination and lasts one year. Following the first booster vaccination protection lasts 3 years.

Leucogen is a vaccine. Vaccines work by ‘teaching’ the immune system (the body’s natural defences) how to defend itself against a disease. Leucogen contains small amounts of a protein from the outer layer of the virus called ‘envelope p45 protein’. The FeLV protein used in the vaccine is not extracted from viruses but is made in a bacterium using ‘recombinant technology’. When a cat is given the vaccine the cat’s immune system recognises the protein as ‘foreign’ and makes antibodies against it. In the future, the immune system will be able to produce antibodies more quickly when it is exposed to FeLV, which will help to protect against the disease caused by the virus.

Leucogen also contains aluminium hydroxide gel and extract of Quillaja saponaria as adjuvants (ingredients that strengthen the immune response).

In one field study kittens aged 8 to 9 weeks were given an initial vaccination course of Leucogen with 2 injections 3 weeks apart and an annual booster injection 1 year later. After the first injection 69% of the kittens had antibodies to FeLV and this increased to 100% after the second injection. Some 64% of cats still had FeLV antibodies before the annual booster, and 100% of cats had FeLV antibodies after the booster.

In a second study, kittens aged 8-9 weeks were given an initial vaccination course of a combination vaccine consisting of one dose of Feligen RCP (against feline rhinotracheitis virus, feline calicivirus and feline panleucopenia virus) with one dose of Leucogen. After the second injection, 100% of kittens had antibodies to FeLV.

A laboratory study in which cats were exposed to feline leukaemia virus confirmed that following the first annual booster vaccination cats were protected for a three year period against leukaemia.

The most common side effects with Leucogen (which may affect up to 1 in 10 cats) are a moderate and short-lived local reaction (<2 cm) after the first injection which resolves without treatment within 3 to 4 weeks, raised body temperature (lasting 1 to 4 days), apathy (listlessness) and digestive disturbances.

Leucogen must not be used in pregnant cats.

For the full list of restrictions and all side effects reported with Leucogen, see the package leaflet.

In case of accidental self-injection, medical advice should be sought immediately and the package leaflet or label shown to the doctor.

The European Medicines Agency decided that Leucogen’s benefits are greater than its risks and it can be authorised for use in the EU.

Leucogen received a marketing authorisation valid throughout the EU for Leucogen on 17 June 2009.

български (BG) (110.42 KB - PDF)

View

español (ES) (82.45 KB - PDF)

View

čeština (CS) (105.01 KB - PDF)

View

dansk (DA) (79.96 KB - PDF)

View

Deutsch (DE) (81.52 KB - PDF)

View

eesti keel (ET) (79.49 KB - PDF)

View

ελληνικά (EL) (120.33 KB - PDF)

View

français (FR) (81.47 KB - PDF)

View

hrvatski (HR) (100.41 KB - PDF)

View

italiano (IT) (73.53 KB - PDF)

View

latviešu valoda (LV) (104.45 KB - PDF)

View

lietuvių kalba (LT) (103.54 KB - PDF)

View

magyar (HU) (93.32 KB - PDF)

View

Malti (MT) (97.66 KB - PDF)

View

Nederlands (NL) (73.82 KB - PDF)

View

polski (PL) (107.27 KB - PDF)

View

português (PT) (74.34 KB - PDF)

View

română (RO) (95.58 KB - PDF)

View

slovenčina (SK) (106.59 KB - PDF)

View

slovenščina (SL) (95.83 KB - PDF)

View

Suomi (FI) (89.53 KB - PDF)

View

svenska (SV) (73.65 KB - PDF)

View

Product information

български (BG) (197.26 KB - PDF)

View

español (ES) (159.58 KB - PDF)

View

čeština (CS) (185.76 KB - PDF)

View

dansk (DA) (165.88 KB - PDF)

View

Deutsch (DE) (159.55 KB - PDF)

View

eesti keel (ET) (157.37 KB - PDF)

View

ελληνικά (EL) (202 KB - PDF)

View

français (FR) (156.4 KB - PDF)

View

hrvatski (HR) (177.35 KB - PDF)

View

íslenska (IS) (158.99 KB - PDF)

View

italiano (IT) (157.22 KB - PDF)

View

latviešu valoda (LV) (187.15 KB - PDF)

View

lietuvių kalba (LT) (182.97 KB - PDF)

View

magyar (HU) (184.87 KB - PDF)

View

Malti (MT) (199.56 KB - PDF)

View

Nederlands (NL) (153.35 KB - PDF)

View

norsk (NO) (154.09 KB - PDF)

View

polski (PL) (185.75 KB - PDF)

View

português (PT) (162.18 KB - PDF)

View

română (RO) (188.86 KB - PDF)

View

slovenčina (SK) (187.9 KB - PDF)

View

slovenščina (SL) (179.01 KB - PDF)

View

Suomi (FI) (151.54 KB - PDF)

View

svenska (SV) (152.06 KB - PDF)

View

Latest procedure affecting product information: IG-1409

07/10/2021

български (BG) (53.76 KB - PDF)

View

español (ES) (35.07 KB - PDF)

View

čeština (CS) (47.18 KB - PDF)

View

dansk (DA) (30.76 KB - PDF)

View

Deutsch (DE) (30.8 KB - PDF)

View

eesti keel (ET) (30.51 KB - PDF)

View

ελληνικά (EL) (51.83 KB - PDF)

View

français (FR) (30.61 KB - PDF)

View

hrvatski (HR) (39.25 KB - PDF)

View

íslenska (IS) (30.32 KB - PDF)

View

italiano (IT) (30.86 KB - PDF)

View

latviešu valoda (LV) (51.56 KB - PDF)

View

lietuvių kalba (LT) (47.34 KB - PDF)

View

magyar (HU) (36.41 KB - PDF)

View

Malti (MT) (49.73 KB - PDF)

View

Nederlands (NL) (30.66 KB - PDF)

View

norsk (NO) (31.17 KB - PDF)

View

polski (PL) (48.78 KB - PDF)

View

português (PT) (30.7 KB - PDF)

View

română (RO) (48.57 KB - PDF)

View

slovenčina (SK) (46.93 KB - PDF)

View

slovenščina (SL) (38.38 KB - PDF)

View

Suomi (FI) (30.41 KB - PDF)

View

svenska (SV) (30.37 KB - PDF)

View

Product details

Name of medicine
Leucogen
Active substance
purified p45 FeLV-envelope antigen
International non-proprietary name (INN) or common name
Feline leukaemia vaccine (inactivated)
Species
Cats
Anatomical therapeutic chemical veterinary (ATCvet) code
QI06AA01

Pharmacotherapeutic group

  • Immunologicals for felidae
  • Inactivated viral vaccines
  • feline leukaemia virus

Therapeutic indication

Active immunisation of cats from eight weeks of age against feline leukaemia for the prevention of persistent viraemia and clinical signs of the related disease.

Authorisation details

EMA product number
EMEA/V/C/000144
Marketing authorisation holder
Virbac S.A.

1ère Avenue 2065 M - L.I.D.
06516 Carros Cedex
France

Marketing authorisation issued
17/06/2009
Revision
8

Assessment history

This page was last updated on

Share this page