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Clinical Trial Summary

Section 1: The purpose of the study is to obtain safety and immunogenicity data of different dose levels of a multivalent recombinant OspA Lyme Borreliosis (mv rOspA LB) Vaccine with and without adjuvant in seronegative healthy adults aged 18 to 70 years. The outcome shall provide the basis for dose/formulation selection for Section 2 of the study. Section 2: An additional purpose of the study is to evaluate the safety and immunogenicity of the optimal dose(s)/formulation of the mv rOspA LB Vaccine in a larger population of seronegative and seropositive healthy subjects aged 18 to 70 years.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT01504347
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 1, 2011
Completion date February 28, 2014