Key Insights

Highlights

Success Rate

79% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 37/100

Termination Rate

18.8%

3 terminated out of 16 trials

Success Rate

78.6%

-7.9% vs benchmark

Late-Stage Pipeline

13%

2 trials in Phase 3/4

Results Transparency

91%

10 of 11 completed with results

Key Signals

10 with results79% success

Data Visualizations

Phase Distribution

13Total
Not Applicable (2)
P 1 (3)
P 2 (6)
P 3 (2)

Trial Status

Completed11
Terminated3
Active Not Recruiting2

Trial Success Rate

78.6%

Benchmark: 86.5%

Based on 11 completed trials

Clinical Trials (16)

Showing 16 of 16 trials
NCT06813872Active Not RecruitingPrimary

Effectiveness of ABRYSVO® Maternal Respiratory Syncytial Virus (RSV) Vaccine Against RSV in Infants in Western Pennsylvania

NCT06077968Active Not RecruitingPrimary

A Study to Learn About ABRYSVO Vaccine in Older Adults to Prevent Severe Respiratory Syncytial Virus (RSV) Disease

NCT04908683Phase 3CompletedPrimary

A Study of an Adenovirus Serotype 26 Pre-fusion Conformation-stabilized F Protein (Ad26. RSV. preF) Based Respiratory Syncytial Virus (RSV) Vaccine in the Prevention of Lower Respiratory Tract Disease in Adults Aged 60 Years and Older

NCT03303625Phase 1CompletedPrimary

A Study to Evaluate the Safety, Tolerability and Immunogenicity of an Investigational RSV Vaccine Candidate (Ad26.RSV.preF) in Adults 18 to 50 Years of Age, and RSV-seropositive Toddlers 12 to 24 Months of Age

NCT03982199Phase 2TerminatedPrimary

A Study of an Ad26.RSV.preF-based Regimen in the Prevention of Reverse Transcriptase Polymerase Chain Reaction (RT-PCR)-Confirmed Respiratory Syncytial Virus (RSV)-Mediated Lower Respiratory Tract Disease in Adults Aged 65 Years and Older

NCT05966090Phase 3CompletedPrimary

A Study on Safety and Immune Response of Investigational RSV OA Vaccine in Combination With Herpes Zoster Vaccine in Healthy Adults

NCT04068792Phase 2CompletedPrimary

A Two-Part Infant Study for Early Diagnosis of Respiratory Syncytial Virus (RSV) and Evaluation of JNJ-53718678 in RSV Acute Respiratory Tract Disease

NCT05712460Phase 1CompletedPrimary

A Study to Assess the Safety, Effects and Palatability of Sisunatovir in Healthy Adult Participants

NCT04086472Phase 2CompletedPrimary

Phase 2a Respiratory Syncytial Virus (RSV) Human Challenge Study of Clesrovimab (MK-1654) in Healthy Participants (MK-1654-005)

NCT03026348Phase 2CompletedPrimary

Safety and Immunogenicity Study to Evaluate Single- or Two-Dose Regimens Of RSV F Vaccine With and Without Aluminum Phosphate or Matrix-M1™ Adjuvants In Clinically-Stable Older Adults

NCT02935673Phase 2TerminatedPrimary

Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine Regimens in Adult Participants Hospitalized With Respiratory Syncytial Virus

NCT03333317Phase 2TerminatedPrimary

A Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine (JNJ-64041575) Regimens in Hospitalized Infants and Children Aged 28 Days to 36 Months Infected With Respiratory Syncytial Virus

NCT01249625Not ApplicableCompleted

The Respiratory Protection Effectiveness Clinical Trial

NCT02561871Phase 1CompletedPrimary

A Study to Evaluate the Safety, Tolerability and Immunogenicity of Ad26.RSV.FA2 Followed by Ad35.RSV.FA2 in Healthy Adult Volunteers

NCT00585481CompletedPrimary

Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian Children

NCT00263900Not ApplicableCompleted

TGV:Use of the Quick Diagnostic Test of the Influenza and the Infection With RSV by the Paediatric Emergency Unit

Showing all 16 trials

Research Network

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