Key Insights

Highlights

Success Rate

94% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

5.6%

1 terminated out of 18 trials

Success Rate

94.1%

+7.6% vs benchmark

Late-Stage Pipeline

67%

12 trials in Phase 3/4

Results Transparency

19%

3 of 16 completed with results

Key Signals

3 with results94% success

Data Visualizations

Phase Distribution

16Total
P 2 (4)
P 3 (4)
P 4 (8)

Trial Status

Completed16
Terminated1
Withdrawn1

Trial Success Rate

94.1%

Benchmark: 86.5%

Based on 16 completed trials

Clinical Trials (18)

Showing 18 of 18 trials
NCT03932448Withdrawn

Fever After Tick Bite Study

NCT00840801Phase 3CompletedPrimary

Immunogenicity, Safety and Interchangeability of Two Tbe Vaccines Administered According to a Conventional Schedule in Children

NCT00460486Phase 3CompletedPrimary

Immunogenicity and Safety Study of FSME-IMMUN 0.5 mL in Adult Subjects Previously Vaccinated According to a Rapid Immunization Schedule

NCT00894686Phase 4CompletedPrimary

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)

NCT01031537Phase 2Terminated

Vaccine Study for Tick-Borne Encephalitis Virus (TBEV)

NCT00161954Phase 4CompletedPrimary

Immunogenicity and Safety Study of a Rapid Immunization Schedule With FSME-IMMUN 0.5 mL in Healthy Adults Aged 16 - 65 Years

NCT00163540Phase 4CompletedPrimary

Immunogenicity and Safety Study of a Third Vaccination With FSME-IMMUN 0.5 mL in Subjects Previously Vaccinated According to a Rapid Immunization Schedule (Follow-up to Study 225)

NCT00161746Phase 2CompletedPrimary

Safety and Immunogenicity Study of 3 Vaccinations With TICOVAC in 2 Dosages in Healthy Children Aged Between 6 Months and 3 Years

NCT00161876Phase 3CompletedPrimary

FSME IMMUN NEW Follow-up to Study 208 in Volunteers Aged 16 to 66 Years

NCT00161824Phase 3CompletedPrimary

Safety Study in Volunteers From 16 to 65 Years of Age: FSME IMMUN NEW vs. ENCEPUR

NCT00503529Phase 4CompletedPrimary

TBE Antibody Persistence and Booster Vaccination Study in Adults (Follow-up to Study 223)

NCT00163618CompletedPrimary

Study to Investigate the Seropersistence of TBE Virus Antibodies Approx. 3 Years After a Booster Vaccination With FSME-IMMUN 0.25 mL JUNIOR in Children

NCT00161967Phase 4CompletedPrimary

TBE Antibody Persistence and Booster Vaccination Study in Children and Adolescents (Follow-up to Study 209)

NCT00161850Phase 2CompletedPrimary

FSME IMMUN NEW Follow-up to Study 199 in Children Aged 1 to 6 Years

NCT00161889Phase 2CompletedPrimary

FSME IMMUN NEW Follow-up to Study 205 in Children Aged 6 to 16 Years

NCT00452621Phase 4CompletedPrimary

Evaluation of Long-Term Immunogenicity in Children and Adolescents Boosted With a New Pediatric TBE Vaccine After Five Years

NCT00311441Phase 4CompletedPrimary

Study of the Safety, Tolerability and Immune Response of TBE Vaccines Administered to Healthy Children

NCT00311493Phase 4CompletedPrimary

Evaluation of Long-Term Immunogenicity in Subjects Boosted With a TBE Vaccine for Adults

Showing all 18 trials

Research Network

Activity Timeline