Recommended for the vaccination of healthy cats 12 weeks of age or older for prevention of disease due to rabies virus. Information provided by (Responsible Party): Sanofi ( Sanofi Pasteur, a Sanofi Company ), Participants will receive the Purified Vero Rabies Vaccine (VRVg), Participants will receive the Imovax® Rabies vaccine, Rabies virus neutralizing antibody titer will be determined by the rapid fluorescent focus inhibition test (RFFIT). If experienced, these tend to have a Less Severe expression. Purevax Rabies is used to vaccinate cats from 12 weeks of age to protect against rabies infection.. A 1-ml dose of Purevax Rabies is injected under the skin. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Cost. Data sources include IBM Watson Micromedex (updated 7 Dec 2020), Cerner Multum™ (updated 4 Dec 2020), ASHP (updated 3 Dec 2020) and others. Genetic and Rare Diseases Information Center, U.S. Department of Health and Human Services, The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Purevax Rabies suspension for injection. Like other inactivated vaccines, the initial dose of a rabies vaccine serves as the “priming” dose. Manufactured By MERIAL INC., Athens, GA 30601 USA, Distributed In Canada By MERIAL CANADA, INC., Baie d’Urfé, (Québec), H9X 3V1, Canada, Copyright © 2020 Animalytix LLC. Feline Rhinotracheitis-Calici-Panleukopenia-Chlamydia Psittaci-Rabies Vaccine, Modified Live Virus and Chlamydia, Canarypox Vector. In addition, human rabies immunoglobulins (HRIG) will be concomitantly administered to all subjects on Day 0. Rabies virus vaccine is an exception. First and foremost, a rabies vaccine will prevent against infection, which though slim, can still happen. PUREVAX vaccines are designed for cats and kittens and deliver a robust, effective immune response without the need for adjuvants. A prospective subject should not be included in the study until the condition has resolved or the febrile event has subsided, Identified as an Investigator or employee of the Investigator or study center with direct involvement in the proposed study, or identified as an immediate family member (i.e., parent, spouse, natural or adopted child) of the Investigator or employee with direct involvement in the proposed study. However, it remains the responsibility of the readers to familiarize themselves with the product information contained on the US product label or package insert. PureVax™ Feline Rabies (3 Year) MERIAL LTD. See My Price. Find out answers to common questions about what the vaccine is and when to vaccinate. Study of Purified Vero Rabies Vaccine and Rabies Human Diploid Cell Vaccine in a Simulated Rabies Post-exposure Regimen. PRECAUTIONS: Store at 2-7°C (35-45°F). If a dog, after having received only 1 dose of rabies vaccine, is subsequently exposed to virulent rabies virus, exposure to the virulent virus then serves as … Side Effects. Description. INDICATIONS: PUREVAX® Feline 4/Rabies is recommended for the vaccination of healthy cats 8 weeks of age and older for prevention of disease due to feline rhinotracheitis, calici, panleukopenia, and rabies viruses and as an aid in the reduction of disease due to Chlamydia psittaci. For general information, Learn About Clinical Studies. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Federal government websites often end in .gov or .mil. INDICATIONS: PUREVAX ® Feline 4/Rabies is recommended for the vaccination of healthy cats 8 weeks of age and older for prevention of disease due to feline rhinotracheitis, calici, panleukopenia, and rabies viruses and as an aid in the reduction of disease due to Chlamydia psittaci. The vCP65 strain encoding the rabies G protein [canarypox virus–expressing rabies glycoprotein (ALVAC-RG)] ... the better cost-effective strategy to control rabies is vaccination of both livestock and wildlife. one at Day 0, at Day 3, at Day 7, at Day 14 and at Day 28, respectively, (Essen regimen). Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01877395. Education on dog behaviour and bite prevention for both children and adults is an essential extension of a rabies vaccination programme and can decrease both the incidence of human rabies and the financial burden of treating dog bites. Vaccination plays a vital role in protecting cats from infectious diseases, some of which are potentially fatal.They can be exposed to these diseases from their environment, other pets, or even humans. Click here to learn more about feline leukemia and the FVRCP vaccine. The cost is $24.85 for an adult cat. Contains a nonadjuvanted lyophilized suspension of a recombinant vectored rabies vaccine; Subcutaneous injection; 20.5.2.2 Rabies. Subject is pregnant, or lactating, or of childbearing potential (to be considered of non-childbearing potential, a female must be post-menopausal for at least 1 year, surgically sterile, or using an effective method of contraception or abstinence from at least 4 weeks prior to the first vaccination and until at least 4 weeks after the last vaccination), Participation at the time of study enrollment or planned participation during the present trial period in another clinical trial investigating a vaccine, drug, medical device, or medical procedure, Receipt of any vaccine in the 4 weeks preceding the first trial vaccination or planned receipt of any vaccine during the course of the trial, Previous vaccination against rabies (in pre- or post-exposure regimen) with either the trial vaccine or another vaccine, Receipt of immunoglobulins, blood or blood-derived products in the past 3 months, Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy, such as anti-cancer chemotherapy or radiation therapy, within the preceding 6 months; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months), Self-reported seropositivity for Human Immunodeficiency Virus (HIV), Hepatitis B, or Hepatitis C, At high risk of rabies infection during the trial, Known systemic hypersensitivity to any of the components of either vaccine or HRIG, or history of a life-threatening reaction to the vaccines used in the trial or to a vaccine containing any of the same substances, Self-reported thrombocytopenia, contraindicating intramuscular (IM) vaccination, Bleeding disorder, or receipt of anticoagulants in the 3 weeks preceding inclusion, contraindicating IM vaccination, Deprived of freedom by an administrative or court order, or in an emergency setting, or hospitalized involuntarily, Chronic illness that, in the opinion of the Investigator, is at a stage where it might interfere with trial conduct or completion, Moderate or severe acute illness/infection (according to investigator judgment) on the day of vaccination or febrile illness (temperature ≥ 100.4°F). 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