Key Insights

Highlights

Success Rate

98% trial completion (above average)

Published Results

104 trials with published results (43%)

Research Maturity

205 completed trials (84% of total)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

1.6%

4 terminated out of 244 trials

Success Rate

98.1%

+11.5% vs benchmark

Late-Stage Pipeline

65%

158 trials in Phase 3/4

Results Transparency

51%

104 of 205 completed with results

Key Signals

104 with results98% success

Data Visualizations

Phase Distribution

220Total
Not Applicable (12)
P 1 (20)
P 2 (30)
P 3 (109)
P 4 (49)

Trial Status

Completed205
Unknown11
Not Yet Recruiting10
Recruiting6
Terminated4
Active Not Recruiting4

Trial Success Rate

98.1%

Benchmark: 86.6%

Based on 205 completed trials

Clinical Trials (244)

Showing 20 of 20 trials
NCT07598890Phase 1Active Not RecruitingPrimary

Phase I Clinical Trial of Adsorbed Tetanus Vaccine

NCT07807033Not Yet RecruitingPrimary

Observation of Immune Persistence in a Clinical Trial of an Adsorbed Tetanus Vaccine

NCT06947499Phase 2Active Not Recruiting

A Phase II/III Study to Evaluate the Immunogenicity, Safety and Lot-to-lot Consistency of LBVD, a Fully Liquid Hexavalent Diphtheria-tetanus-whole Cell Pertussis-hepatitis B-poliovirus-Haemophilus Influenzae Type b Conjugate (DTwP-HepB-IPV-Hib) Vaccine, in Healthy Infants as Primary Series

NCT05457946Phase 2Completed

Study to Evaluate the Immunogenicity and Safety of LBVD(Hexavalent Vaccine), Given to Healthy Infants at Primary Series

NCT05664750Phase 3CompletedPrimary

Study to Compare the Efficacy and Safety of Passive Immunization With TNM002 Injection and Human Tetanus Immunoglobulin as Prophylaxis Against Tetanus

NCT07793513Phase 3Not Yet Recruiting

Study of BK1803 in Healthy Infants

NCT06708286Phase 2Completed

A Clinical Trials of Adsorbed Cell-free DPT Vaccine (Five-component)

NCT06056050Phase 1Completed

A Clinical Trial of Adsorbed Cell-free DPT Vaccine (5-component) (for People Aged 6 Years and Above)

NCT06120751Phase 3CompletedPrimary

A Clinical Trial to Evaluate the Safety and Immunogenicity of a Single Dose of Adsorbed Tetanus Vaccine in a Population Aged 18 Years and Over

NCT07744347Not Yet Recruiting

A Clinical Study on Immunogenicity Persistence of Adsorbed 5-component Acellular Pertussis, Diphtheria and Tetanus Combined Vaccine

NCT07740733Phase 3CompletedPrimary

Phase I/III Clinical Trial of Adsorbed Tetanus Vaccine

NCT07347938RecruitingPrimary

A Phase 4 Study to Evaluate the Effectiveness and Safety of Siltartoxatug Injection for Tetanus Prophylaxis Following Injury

NCT07724379CompletedPrimary

A Study of Tetanus Antibody of Healthy Adults

NCT07633119Phase 3Not Yet RecruitingPrimary

A Phase Ⅲ Clinical Study of SNA02-48 Injection

NCT07624669Phase 4Not Yet Recruiting

A First in Human Study Investigating the Safety of an Unloaded and Loaded (With a Tetanus-containing Vaccine Booster) Microneedle Patch in Healthy Adults

NCT06939777Phase 1CompletedPrimary

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SNA02-48 Injection in Chinese Adult Participants

NCT07621341Phase 4Not Yet Recruiting

Maternal Immunization With Tetanus Toxoid, Reduced Diphtheria Toxoid, Reduced-dose (2 µg) Recombinant Pertussis Vaccine (TdaP2gen) and Its Effect on the Immune Response in Thai Infants up to 15-18 Months Old

NCT07492303Phase 1Not Yet Recruiting

A Phase I Clinical Trial of Absorbed Acellular Pertussis (Two-Component) Diphtheria-Tetanus Combined Vaccine (For Adults and Adolescents)

NCT07446166Not ApplicableNot Yet RecruitingPrimary

TETANUS Antibody Detection in Saliva Study

NCT07444502Completed

Safety Monitoring of Boostagen® Vaccine in Thailand

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