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Study identifier: NCT06255626 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Safety and Immunogenicity of a Sub-unit Protein CD40.RBDv Bivalent COVID-19 Vaccine, Adjuvanted or Not, as a Booster in Volunteers.

Condition: COVID-19  ·  Sponsor: ANRS, Emerging Infectious Diseases

PhasePhase 1/Phase 2
Planned participants215
Who can joinAll sexes, 18 Years to 84 Years
Healthy volunteersYes

About this study

The goal of this clinical trial, on healthy volunteers, is to learn more about safety and reactogenicity of the CD40.RBDv vaccine. The main questions that will be studied are : * Is the CD40.RBDv (adjuvanted or not) safe ? * Does the CD40.RBDv (adjuvanted or not) imply an immunologic response ? Participants will receive, depending on their randomization arm, 1 or 2 injections of the CD40.RBDv vaccine or a single injection of approved mRNA vaccine

This description comes directly from the study's public registry record.

Talk to the study team

Yves Levy, MD  ·  +33149814442  ·  yves.levy@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (2)

Hopital Henri MondorCréteil, FranceRecruiting
Hôpital CochinParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06255626