None listed
Conditions
Interventions
A Phase III follow-up study to assess long term safety 6 months after the first vacccination with IC51 and to assess in a subgroup the long term immunogenicity up to 24 months
Sponsors
Intercell AG
Study design
Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Healthy subjects. Written informed consent obtained prior to study entry.
Exclusion criteria
No exclusion criteria
Outcome results
None listed