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Tick-Borne Encephalitis

Part of Flavivirus Infections

1 published article · Updated continuously

Clinical Trial Landscape

Clinical Trials for Tick-Borne Encephalitis

5 trials tracked for Tick-Borne Encephalitis: 4 in phase 3 or 4 and 2 with published results. The most-cited published study has 18 citations.

5Trials tracked
4Phase 3 & 4
0Recruiting
2With published results
Phase distribution
Phase 4 2 Phase 3 2 Phase 2 1
  1. Phase 4 Tick-Borne Encephalitis (TBE) Seropersistence After First Booster and Response to a Second Booster in Children, Adolescents and Young Adults (Follow-Up to Study 700401) Completed · 18 cited
  2. Phase 3 Study to Evaluate the Immunogenicity, Safety, and Tolerability of a Tick-Borne Encephalitis (TBE) Vaccine in Healthy Japanese Participants 1 Year of Age and Older Completed · 2 cited
  3. Phase 4 Study to Evaluate Long Term Immunogenicity up to 10 Years After the First Booster Immunization With Tick Borne Encephalitis Vaccine in Adults Who Received 1 of 3 Different Primary Vaccination Schedules Completed
  4. Phase 3 Immunogenicity, Safety and Interchangeability of Two Tbe Vaccines Administered According to a Conventional Schedule in Children Completed
  5. Phase 2 Humoral and Cellular Immunity for TBE Vaccination in Allogeneic HSCT Recipients Completed

Showing the 5 most-cited and recently-updated of 5 trials. Browse the full registry →

Trial data sourced from ClinicalTrials.gov. Counts describe the research landscape and are not a treatment recommendation. Informational only — not medical advice.

What the trials found For clinicians

Tick-Borne Encephalitis: what the trials found

Vaccination for Tick-Borne Encephalitis (TBE) demonstrates high seropositivity rates across multiple study designs and formulations. Specifically, studies using FSME-IMMUN 0.25 mL Junior or 0.5 mL reported a 100% seropositivity rate via Neutralization Test (NT) at both 21-35 days and up to 46 months following the first booster vaccination 1.

Inactivated TBE vaccines have shown high efficacy in inducing antibody responses; studies reported seropositivity rates of 97.8% to 100% via NT after the second dose, and 91% to 100% across various intervals following first and third doses 4. Additionally, a 0.5 mL TBE vaccine demonstrated a 98-100% seropositivity rate at 4 weeks after the third dose, with low rates of local reactions observed within 7 days of administration 3.

Monitoring of antibody titers shows high prevalence of detectable responses; studies reported that approximately 89.58% to 100% of subjects achieved TBE antibody titers ≥ 2, while 89.58% to 94.12% achieved titers ≥ 10 2.

Recent results — preliminary, needs further review

  • A Phase 2 study of a TBE virus vaccine showed significant improvements in Neutralization Test (NT) responses and ELISA antibody concentrations following the second vaccination 5.

For the clinician treating this condition

  • TBE vaccines consistently achieve high seropositivity rates (90-100%) across various dosages and testing methods (NT and ELISA) [1, 4].
  • Long-term immunity is supported by evidence of sustained seropositivity up to 46 months post-booster 1.
  • Vaccine safety profiles indicate low rates of local reactions following administration 3.

AI synthesis of 5 cited trials, updated Jun 29, 2026. Informational only — not medical advice; trial data sourced from ClinicalTrials.gov. How we use AI.

HCP Mode — summaries include clinical detail, trial data, and statistical outcomes.
Patient Mode — summaries use plain language, avoiding clinical jargon.

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