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Vaxart’s norovirus vaccine meets all safety, immunogenicity endpoints in phase 1 clinical trial
South San Francisco, California | Thursday, February 16, 2017, 12:00 Hrs  [IST]

Vaxart, a clinical-stage biotechnology company developing oral recombinant vaccines that are administered by tablet rather than by injection, has announced that its norovirus tablet vaccine met the primary and secondary endpoints for safety and immunogenicity in a Phase 1 clinical trial.

“The norovirus Phase 1 results are an important milestone for our oral vaccine platform as well as for the entire vaccine space,” said Dave Liebowitz, MD, PhD, chief medical officer of Vaxart. “Building on results from previous studies, the tablet vaccine platform has been well tolerated across multiple indications, and we consistently see robust and broad responses for our candidate vaccines. The norovirus results are particularly striking as they were obtained with a single dose of our tablet vaccine.”

The norovirus tablet vaccine was well tolerated in all subjects. Solicited symptoms and unsolicited adverse events were mostly mild in severity with no serious adverse events (SAEs) reported in the study to date. The vaccine also met its immunogenicity endpoint in both dose groups, as measured by a significant increase in the norovirus blocking antibody titers (BT50) in serum. Significant mucosal immune responses were observed as well, and the vaccine generated potent gut homing, memory, and plasmablast B cell activation.

“The norovirus tablet vaccine combines ease of oral delivery with a novel mode of immunization that induces both a local intestinal immune response as well as a systemic antibody response. As a result, the norovirus tablet vaccine generates rapid, robust intestinal immune responses against norovirus,” said Sean Tucker, PhD, chief scientific officer of Vaxart. “We believe that the generation of a potent immune response at the same site as the actual norovirus infection will serve as an effective first line of defense, and may provide better cross protection against divergent strains than serum antibody responses alone.”

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