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Phase I trial shows needle-free pan-Sarbecovirus vaccine is safe with modest immune responses

By

Saul N. Fausta,b,1 Send email to [email protected]

16d ago· 26 min readenNews

Summary

This article reports on a first-in-human Phase I clinical trial of pEVAC-PS, a computationally designed pan-Sarbecovirus vaccine delivered via needle-free intradermal injection. The vaccine, developed using DIOSynVax technology, aims to induce broad cross-protective immune responses across multiple Sarbecoviruses including SARS, SARS-CoV-2, and potential zoonotic threats. The trial found the vaccine to be safe and well-tolerated. While immunogenicity was modest in the context of substantial pre-existing immunity, participants developed measurable responses to conserved, vaccine-encoded sarbecovirus epitopes, supporting the feasibility of this antigen design strategy.

Source

bskyPhase I trial shows needle-free pan-Sarbecovirus vaccine is safe with modest immune responsesjournalofinfection.com

Key quotes

· 3 pulled
Needle-free intradermal delivery of this novel computationally designed PanSarbeco vaccine was safe and well tolerated.
Although immunogenicity was modest in the context of substantial pre-existing immunity, participants developed measurable responses to conserved, vaccine-encoded sarbecovirus epitopes, supporting the feasibility of this antigen design strategy.
The pEVAC-PS vaccine was developed using Digitally Immune Optimised Synthetic Vaccine (DIOSynVax) technology and pre-clinically selected for the ability to induce broadly protective immune responses across the Sarbecoviruses.
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Needle-free intradermal delivery of this novel computationally designed PanSarbeco vaccine was safe and well tolerated. Although immunogenicity was modest in the context of substantial pre-existing immunity, participants developed measurable responses to

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