COPENHAGEN, Denmark, April 16, 2026
Bavarian Nordic A/S has announced that Swissmedic, the Swiss Agency for Therapeutic Products, has granted approval for its VIMKUNYA® chikungunya vaccine (recombinant, adsorbed) for active immunization in individuals aged 12 years and older. This milestone marks the first approval of a chikungunya vaccine in Switzerland, reinforcing the company’s leadership in infectious disease prevention and expanding global access to innovative vaccines targeting emerging viral threats.
Regulatory Milestone Expands Global Vaccine Access
The Swissmedic approval represents the fourth regulatory authorization for VIMKUNYA, following earlier approvals by the U.S. Food and Drug Administration (FDA), the European Commission, and the UK Medicines and Healthcare products Regulatory Agency (MHRA) in 2025. The Swiss decision was based on a comprehensive regulatory submission filed in July 2025, supported by clinical and immunogenicity data demonstrating the vaccine’s safety and efficacy.
This latest approval underscores Bavarian Nordic’s strategic commitment to expanding global access to vaccines for emerging infectious diseases, particularly those with increasing geographic spread. The company has also submitted an application to Health Canada, with a potential decision expected in the first half of 2026, further strengthening its international regulatory footprint.
Leadership at Bavarian Nordic emphasized that the Swiss approval is a key step in delivering protection against chikungunya to broader populations, especially in regions at risk of outbreaks. The growing list of approvals highlights strong regulatory confidence in the vaccine’s clinical profile and public health value.
Innovative VLP Vaccine Technology and Clinical Benefits
VIMKUNYA is a single-dose, prefilled, adjuvanted virus-like particle (VLP) recombinant protein vaccine, designed to provide rapid and robust immune protection against chikungunya virus (CHIKV). The vaccine induces a strong seroresponse, with protective immunity developing as early as one week after administration, making it particularly valuable in outbreak settings and travel-related exposures.
Unlike traditional vaccines, VIMKUNYA does not contain viral genetic material, making it non-infectious and incapable of causing disease. This feature enhances its safety profile and allows for broader use across diverse populations. The convenience of a single-dose regimen combined with rapid onset of immunity positions the vaccine as a highly effective tool in preventing chikungunya infections.
The use of advanced VLP technology reflects a growing trend in vaccine development, where structural mimicry of viruses enables strong immune responses without the risks associated with live or attenuated pathogens. This innovation is expected to play a significant role in combating emerging viral diseases globally.

