MVA-BN-EBV for EBV Infection
What You Need to Know Before You Apply
What is the purpose of this trial?
Phase 1, single-center, randomized, placebo-controlled, double-blind clinical trial.
Participants (N = 15) will receive a 2-dose schedule (1 vaccination on day 1 and day 28) randomized, receiving either MVA-BN-EBV (n = 12) or placebo (n = 3).
Are You a Good Fit for This Trial?
This trial is for healthy young adults who do not have any serious medical conditions. Participants should not have a history of EBV infection or immune system problems, and must be able to attend all study visits.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- MVA-BN-EBV
Trial Overview
The study is testing the safety and immune response of an experimental vaccine called MVA-BN-EBV compared to a placebo. Participants are randomly assigned to receive two doses (on day 1 and day 28) in a double-blind manner.
How Is the Trial Designed?
2
Treatment groups
Active Control
Placebo Group
Liquid frozen suspension of MVA-BN-EBV vaccine (distributed in single dose vials) will contain at least 3 × 108 Inf.U per 0.5 mL. MVA-BN-EBV vaccine will be given by intramuscular (IM) administration into the deltoid of the upper arm (preferably the non-dominant arm). Each participant will receive 2 vaccinations, 28 days apart.
One dose of 0.5 mL placebo contains 0.605 mg trometamol (tris-hydroxymethyl-amino methane) and 4.09 mg sodium chloride (TBS). It is administered as an IM injection into the deltoid of the upper arm (preferably the non-dominant arm). Each participant will receive 2 vaccinations, 28 days apart.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Bavarian Nordic
Lead Sponsor
Paul Chaplin
Bavarian Nordic
Chief Executive Officer since 2014
PhD in Immunology from Bristol University
Jean-Christophe May
Bavarian Nordic
Chief Medical Officer since 2020
PharmD and MBA
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