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Related news from
Tue, 16 Oct 2018
05:01:10 +0000
VALNEVA Announces Progress of Chikungunya Vaccine Candidate
The Company has now commenced the second stage of its Phase 1 study. This re-vaccination will act as an intrinsic human challenge, with the goal of demonstrating that subjects are protected from vaccine-induced viremia early in the VLA1553 clinical development.
Fri, 05 Oct 2018
05:01:09 +0000
VALNEVA Announces FDA Approval of Accelerated IXIARO® Vaccination Schedule
Valneva SE ("Valneva" or "the Company"), a commercial stage biotech company focused on developing innovative lifesaving vaccines, announced today that the U.S. Food and Drug Administration (FDA) has approved an alternate IXIARO® immunization schedule of two doses administered seven days apart for adult travelers aged 18-65 years old. This accelerated schedule comes in addition to the previously approved schedule. IXIARO® is the only Japanese encephalitis (JE) vaccine licensed and available in the United States (U.S.).



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