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Clinical Trial Summary

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


Clinical Trial Description

Phase 1/2a randomized, multicentre trial with four cohorts of two arms in two parts. Part 1: Cohort 1: Low dose (LD) CD40.RBDv vaccine non adjuvanted or mRNA vaccine (5:1 ratio) Cohort 2: LD CD40.RBDv vaccine adjuvanted or mRNA vaccine (5:1 ratio) Cohort 3: High dose (HD) CD40.RBDv vaccine non adjuvanted or mRNA vaccine (5:1 ratio) Cohort 4: SC injection of HD CD40.RBDv vaccine adjuvanted or mRNA vaccine (5:1 ratio) Go-criterion for opening enrolment within cohorts are detailed into the protocol. Part 2 at Month 3 : Group 1: Volunteers who received mRNA vaccine in Part 1 will not receive any vaccine Group 2: Volunteers who received a first dose of CD40.RBDv vaccine (adjuvanted or not) in Part 1 but randomized (1:1) to receive no further dose of vaccine in Part 2. Group 3: Volunteers who received a first dose of CD40.RBDv vaccine (adjuvanted or not) in Part 1 and randomized (1:1) to receive an additional dose of CD40.RBDv vaccine (adjuvanted or not) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06255626
Study type Interventional
Source ANRS, Emerging Infectious Diseases
Contact Yves Levy, MD
Phone +33149814442
Email yves.levy@aphp.fr
Status Recruiting
Phase Phase 1/Phase 2
Start date May 27, 2024
Completion date September 2025

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