Prophylaxis of Lyme Borreliosis
Conditions
Brief 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.
Interventions
BIOLOGICALMultivalent recombinant OspA Lyme Borreliosis Vaccine
Primary vaccination (6 study arms of 50 subjects each): 3 intramuscular injections containing either dose A, B or C in an adjuvanted or non-adjuvanted formulation (6 different formulations) given in monthly intervals (recruited in 3 sequential cohorts)
Sponsors
Baxter Innovations GmbH
Baxalta now part of Shire
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
Main Inclusion Criteria: * Subject is 18 to 70 years old at the time of screening * Subject has an understanding of the study, agrees to its provisions, and gives written informed consent prior to study entry * Subject is generally healthy, as determined by the investigator's clinical judgment through collection of medical history and the performance of a physical examination * If female of childbearing potential, presents with a negative urine pregnancy test, and agrees to employ adequate birth control measures for the duration of the study Additional inclusion criterion for seropositive subjects in Section 2 only: \- Subject is seropositive for Borrelia burgdorferi sensu lato (s.l.) antibodies at study entry Main
Exclusion criteria
* Subject has a physician-diagnosed chronic illness related to Lyme borreliosis (LB) or active LB * Subject has been treated for LB with antibiotics within 3 months of study entry * Subject had a tick bite within 3 weeks prior to screening or first vaccination * Subject has a history or active infection with Babesia microti (babesiosis) or Anaplasma phagocytophilum (ehrlichiosis) * Subject currently has or has a history of significant cardiovascular, respiratory (including asthma), metabolic, neurological, hepatic, rheumatic, autoimmune, hematological, gastrointestinal or renal disorder * Subject has clinically significant abnormal laboratory values at screening * Subject currently has or has a history of immunodeficiency * Subject tests positive for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) * Subject has a disease or is currently undergoing a form of treatment or was undergoing a form of treatment within 30 days prior to study entry that could be expected to influence immune response. * Subject has a history of anaphylaxis or severe allergic reactions * Subject has received any live vaccine within 4 weeks or inactivated vaccine within 2 weeks prior to vaccination in this study * Subject is pregnant or lactating at the time of study enrollment Additional exclusion criterion for subjects in Section 1 and seronegative subjects in Section 2: \- Subject is seropositive for Borrelia burgdorferi sensu lato (s.l.) antibodies at study entry
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Antibody response to the vaccine | 28 days after the third vaccination (= Day 85) |
| Frequency and severity of injection site and systemic reactions | Within 7 days after each vaccination (i.e. Days 8, 36 and 64) |
Secondary
| Measure | Time frame |
|---|---|
| Antibody response | At baseline, 28 days after each vaccination (i.e. Days 29, 57 and 85), 180 and 270 days after the first vaccination (Day 181, Day 271) and 180 days after the booster vaccination (Day 361 or Day 451 - 546) |
| Fold increase in antibody titer compared to baseline | 28 days after each vaccination, 180 and 270 days after the first vaccination and 180 days after the booster vaccination |
| Seroconversion rate (at least 4-fold increase of each rOspA type-specific Immunoglobulin G (IgG) titer) as compared to baseline | 28 days after each vaccination, 180 and 270 days after the first vaccination and 180 days after the booster vaccination |
| Frequency and severity of adverse events | 28 days after each vaccination and during entire study period |
Countries
Austria, Germany
Outcome results
None listed