Sources: Valneva Press Release, Clinical Trials Arena
Valneva has initiated a Phase I clinical trial to assess the safety and immunogenicity of its VLA1553 vaccine for Chikungunya, a viral disease transmitted by mosquitoes. The randomized trial, conducted in the US, will evaluate three different doses of the vaccine in approximately 120 healthy adults. The study will also assess antibody persistence and re-vaccination at six and 12 months to determine the vaccine's potential efficacy. Initial data from the trial is expected to be available early next year. Valneva aims to develop a single-dose vaccine that provides long-lasting protection against Chikungunya, offering safety for immunization in both adults and children.
Chikungunya is a viral disease caused by the chikungunya virus, transmitted by Aedes mosquitoes. It leads to symptomatic illness in a high percentage of people, causing fever, joint and muscle pain, headache, nausea, rash, and chronic joint pain. The virus can cause large outbreaks, affecting a significant portion of the population in areas where it is present. Travellers to endemic regions, such as parts of Africa, Southeast Asia, and the Americas, are at risk. The virus has spread to over 110 countries, with more than three million reported cases in the Americas alone. The economic impact of chikungunya is significant, and the medical and economic burden is expected to grow as the virus spreads further. Currently, there are no preventive vaccines or effective treatments available, making chikungunya a major public health threat.