VLA1553 for Chikungunya Earns Breakthrough Therapy Status

The FDA has a series of designations it grants to drugs or biologics intending to treat rare, serious, or life-threatening conditions. One of these is Breakthrough Therapy designation. According to MPR, VLA1553, an investigational vaccine to protect against Chikungunya virus (or Chikungunya disease), recently received Breakthrough Therapy designation from the FDA.

VLA1553

Over the past year, there have been over 3 million reported cases of chikungunya throughout the Americas alone, representing a growing burden. However, there are few protective measures in terms of vaccines. VLA1553 is a potential option to overcome this unmet need.

So what is VLA1553? This is the first vaccine against chikungunya being evaluated in Phase 3 clinical trials. This live-attenuated vaccine only requires a single dose to confer protection. Once administered, the vaccine deletes some of the chikungunya virus genome, inhibiting infection and symptoms. According to the drug developer Valneva:

In Phase 1 clinical trials, Valneva observed that VLA1553 led to the development of antibodies to chikungunya in 100% of the 120 healthy participants in this trial.

The vaccine received Breakthrough Therapy designation, which is granted to drugs, used to treat serious conditions, which demonstrate significant improvements (or potential improvements) over available therapies. Once a developer receives this designation, they are also eligible for drug development program guidance and features of Fast Track designation. Outside of Breakthrough Therapy status, VLA1553 has also received PRIME designation in the EU and Fast Track designation in America.