Abstract

In order to obtain Marketing Authorization for an oral rabies vaccine in the European Union, not only safety studies in the target species, red fox and raccoon dog, are required. Since baits are distributed unsupervised in the environment, specific safety studies in selected non-target species are compulsory. Furthermore, oral rabies vaccines are based on live, replication-competent viruses and thus distinct safety studies in the target species for such type of vaccines are also mandatory. Here, the results of these safety studies in target and selected non-target species for a 3rd generation oral rabies virus vaccine construct, SPBN GASGAS (Rabitec), are presented. The studies included the following species; red fox, raccoon dog, domestic dog, domestic cat, domestic pig, wild rodents. The following safety topics were investigated; overdose, repeated dose, dissemination, shedding, horizontal and vertical transmission. It was shown that SPBN GASGAS did not cause disease or any other adverse reaction in vaccinated animals and naïve contact animals. The vaccine did not disseminate within the host beyond the site of entry. No horizontal transmission was observed in wild rodents. In the target species, there was evidence that in a few cases horizontal transmission of vaccine virus could have occurred under these experimental conditions; most likely immediately after vaccine administration. The vaccine construct SPBN GASGAS meets therefore the latest revised minimal safety requirements as laid down in the European Pharmacopoeia.

Highlights

  • A third generation oral rabies virus vaccine SPBN GASGAS (Rabitec) received a positive opinion from the Committee for Medicinal Products for Veterinary Use (CVMP) of the European Medicines Agency (EMA) for oral vaccination of foxes (Vulpes vulpes) and raccoon dogs (Nyctereutes procyonoides) against rabies in the European Union (EU)

  • All animals were kept at the experimental animal facility at IDT Biologika in accordance with the prevailing guidelines and the studies were performed according to European guidelines on animal welfare, clinical endpoints, and care of the Federation of European Laboratory Animal Science Associations (FELASA)

  • The 4 naïve contact cats and dogs remained sero-negative during the observation period, indicating no horizontal transmission of the vaccine virus

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Summary

Introduction

A third generation oral rabies virus vaccine SPBN GASGAS (Rabitec) received a positive opinion from the Committee for Medicinal Products for Veterinary Use (CVMP) of the European Medicines Agency (EMA) for oral vaccination of foxes (Vulpes vulpes) and raccoon dogs (Nyctereutes procyonoides) against rabies in the European Union (EU). This live replication-competent rabies virus vaccine does not express a foreign gene it is considered a genetically modified organism (GMO) due to the genetic modifications realized by site-directed mutagenesis. The results of the above-mentioned studies showed that the vaccine virus SPBN GASGAS did not induce any adverse reaction in target – and non-target species and meets the minimal safety requirements set by the regulatory authorities

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