Valneva’s IXCHIQ® Vaccine Expands Access to Adolescents in Europe
Valneva’s chikungunya vaccine, IXCHIQ®, is now approved for adolescents across Europe.

.webp&w=1920&q=75&dpl=dpl_9xUZQSvr7qh8u3ierG8JmijXnhDf)
Valneva SE has reached a major milestone with the European Commission's approval of its chikungunya vaccine, IXCHIQ®, for adolescents aged 12 and older. This approval follows its previous authorization for adults in July 2024, further strengthening efforts to combat this mosquito-borne virus. With this label extension, the single-dose vaccine is now accessible to adolescents across the EU, Norway, Liechtenstein, and Iceland, offering broader protection against a disease that has long lacked a preventive solution.
IXCHIQ® is the first and only licensed chikungunya vaccine worldwide, marking a breakthrough in global health. Already approved for adults in the U.S., Canada, and the U.K., Valneva is actively seeking similar approvals for adolescents in these regions. With this expanded access, families and healthcare providers now have a powerful tool to safeguard younger populations against chikungunya’s debilitating effects, reinforcing Valneva’s commitment to innovative vaccine solutions.

My international experience as a researcher in Taiwan for three years has equipped me with a global perspective, enabling me to create content that resonates with an international audience.
More from Pharma News
All stories →
Bristol-Myers Squibb Gains FDA Accelerated Approval for Iberdomide in Relapsed or Refractory Multiple Myeloma

Eton Pharmaceuticals Gains FDA Fast Track for AMGLIDIA and Targets 2027 NDA with ASN-001 Acquisition

Discussion