Key Insights

Highlights

Success Rate

90% trial completion (above average)

Published Results

60 trials with published results (35%)

Research Maturity

120 completed trials (71% of total)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

8.2%

14 terminated out of 170 trials

Success Rate

89.6%

+3.0% vs benchmark

Late-Stage Pipeline

19%

33 trials in Phase 3/4

Results Transparency

50%

60 of 120 completed with results

Key Signals

60 with results90% success14 terminated

Data Visualizations

Phase Distribution

142Total
Not Applicable (6)
P 1 (64)
P 2 (39)
P 3 (33)

Trial Status

Completed120
Terminated14
Recruiting10
Unknown9
Active Not Recruiting8
Not Yet Recruiting5

Trial Success Rate

89.6%

Benchmark: 86.5%

Based on 120 completed trials

Clinical Trials (170)

Showing 20 of 20 trials
NCT07214571Phase 2RecruitingPrimary

A Study of S-337395 in Symptomatic Nonhospitalized Adults With Respiratory Syncytial Virus (RSV) Who Are at High Risk of Progression to Severe Disease

NCT07235397Not Yet RecruitingPrimary

Evaluating the Benefits of RSV Maternal Vaccination Using a Scottish National Dataset

NCT06593210Phase 3Active Not Recruiting

RSV Vaccine in Transplant Recipients

NCT07220109Phase 3RecruitingPrimary

A Study on the Immune Response and Safety of Vaccine Against Respiratory Syncytial Virus Given to Chinese Adults 18 to 59 Years of Age at Increased Risk of Respiratory Syncytial Virus Disease

NCT06534892Phase 3Active Not RecruitingPrimary

An Extension and Crossover Vaccination Study on the Immune Response and Safety of a Vaccine Against Respiratory Syncytial Virus Given to Adults 60 Years of Age and Above Who Participated in RSV OA=ADJ-006 Study

NCT06042049Phase 3CompletedPrimary

A Study to Assess Safety, Pharmacokinetics Anti-Drug Antibody and Anti-RSV Antibody After 2 Doses of Nirsevimab

NCT06287450Phase 1Not Yet RecruitingPrimary

A Study to Describe the Safety and Immunogenicity of a Respiratory Syncytial Virus Vaccine IN006 in Healthy Adults

NCT06645665Phase 1Active Not RecruitingPrimary

A Study to Describe the Safety and Immunogenicity of a Respiratory Syncytial Virus Vaccine IN006 in Healthy Adult Aged 18 Years and Above

NCT04732871Phase 3Active Not RecruitingPrimary

Immunogenicity, Safety, Reactogenicity and Persistence of an Investigational Respiratory Syncytial Virus (RSV) Vaccine in Adults Aged 60 Years and Above

NCT05705440Phase 3CompletedPrimary

A Follow-up Study to Describe the Safety of Study Participants Who Received RSVPreF3 Maternal Vaccination (Any Dose) or Controls From Previous RSV MAT Studies During Any Pregnancy Conceived Post Vaccination/Control

NCT07092865Phase 2RecruitingPrimary

A Study Evaluating Persistence of the Immune Response of the Adjuvanted Respiratory Syncytial Virus (RSV) Vaccine and the Safety and Immune Response Following Revaccination in Adults 18 Years of Age and Above Who Received Lung or Kidney Transplant

NCT06083623Phase 2CompletedPrimary

A Trial to Evaluate the Efficacy and Safety of TNM001 for the Prevention of Lower Respiratory Tract Infection Caused by Respiratory Syncytial Virus in Infants

NCT06710925Phase 3CompletedPrimary

A Sudy to Evaluate the Efficacy and Safety of TNM001 in High-risk Infants

NCT06551181Phase 3CompletedPrimary

A Study on the Immune Response, Safety and the Occurrence of Respiratory Syncytial Virus (RSV)-Associated Respiratory Tract Illness After Administration of RSV OA Vaccine in Adults 60 Years and Older

NCT05026749Phase 3RecruitingPrimary

Azithromycin Treatment for Respiratory Syncytial Virus-induced Respiratory Failure in Children

NCT06102174Phase 1TerminatedPrimary

A Study to Learn About the Amount of the Study Medicine (Sisunatovir) in Blood and Its Safety in Infants and Children With Pneumonia Caused by RSV

NCT06374394Phase 3CompletedPrimary

A Study on the Immune Response and Safety of a Vaccine Against Respiratory Syncytial Virus (RSV) When Given Alone and Together With a COVID-19 mRNA Vaccine in Adults Aged 50 Years and Above

NCT06614725Phase 3CompletedPrimary

A Study in India on the Immune Response and Safety of a Respiratory Syncytial Virus (RSV) Older Adults (OA) Vaccine When Given to Older Adults 60 Years of Age and Above and Adults 50-59 Years of Age at Increased Risk (AIR) of Respiratory Syncytial Virus Lower Respiratory Tract Disease (RSV-LRTD)

NCT05655182Phase 1RecruitingPrimary

A Study of BLB-201 RSV Vaccine in Infants and Children

NCT07279298Not Yet RecruitingPrimary

Effectiveness of Immunization in Preventing Severe Acute Respiratory Infection RSV

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