Key Insights

Highlights

Success Rate

96% trial completion (above average)

Published Results

14 trials with published results (42%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

3.0%

1 terminated out of 33 trials

Success Rate

95.8%

+9.3% vs benchmark

Late-Stage Pipeline

12%

4 trials in Phase 3/4

Results Transparency

61%

14 of 23 completed with results

Key Signals

14 with results96% success

Data Visualizations

Phase Distribution

22Total
P 1 (10)
P 2 (8)
P 3 (2)
P 4 (2)

Trial Status

Completed23
Not Yet Recruiting3
Recruiting3
Active Not Recruiting3
Terminated1

Trial Success Rate

95.8%

Benchmark: 86.5%

Based on 23 completed trials

Clinical Trials (33)

Showing 20 of 20 trials
NCT06551506Phase 4Active Not RecruitingPrimary

The Immunology and Safety of Maternal RSV Vaccination (ABRYSVO), Infant Nirsevimab (BEYFORTUS) Immunization, or Both Products

NCT06604767Phase 1CompletedPrimary

Study of a Respiratory Syncytial Virus/Human Metapneumovirus/Parainfluenza Virus Type 3 Vaccine Candidate in Adults Aged 60 Years and Older

NCT07402512Phase 3RecruitingPrimary

A Phase III Study of Deuremidevir Hydrobromide for the Treatment of RSV Infection in Infants and Young Children

NCT07505420Not Yet Recruiting

Risk Factors and Severity of Bronchiolitis in Hospitalized Children at Assiut University Hospital

NCT06134648Phase 1CompletedPrimary

Study of a Respiratory Syncytial Virus/Human Metapneumovirus Vaccine Candidate

NCT06251024Phase 2CompletedPrimary

Study of a Respiratory Syncytial Virus Candidate Formulation in Adults Aged 60 Years and Older

NCT06817889Phase 2Recruiting

Remdesivir for the Treatment of Upper Respiratory Tract Infection Due to RSV in Immunocompromised Individuals

NCT07417657Not Yet RecruitingPrimary

Gut Microbiome and Immune Response in Severe RSV Infection in Vietnamese Infants

NCT04767373Phase 2CompletedPrimary

Efficacy and Safety of Clesrovimab (MK-1654) in Infants (MK-1654-004)

NCT06546800Active Not RecruitingPrimary

SPECIAL INVESTIGATION FOR ABRYSVO IN INDIVIDUALS AGED 60 YEARS OR OLDER

NCT05687279Phase 1CompletedPrimary

Study on a Live-attenuated Respiratory Syncytial Virus Vaccine for Assessment of Safety, Transmissibility, and Genetic Stability of the Vaccine Virus Among Close Contacts in Infants and Toddlers 6 to < 24 Months of Age in Puerto Rico (USA)

NCT07346963Not Yet RecruitingPrimary

RSV-Positive Children <5 Years Presenting to Pediatric Emergency Departments in Türkiye: TRUST-RSV

NCT07239583RecruitingPrimary

Genotype and Disease Burden of RSV in Older Vietnamese Adults (RSV: Respiratory Syncytial Virus )

NCT06079320Phase 2TerminatedPrimary

A Study to Learn About the Study Medicine Sisunatovir in Adults With Respiratory Syncytial Virus (RSV) Infection

NCT06237296Phase 1CompletedPrimary

Study of the Safety and Immune Response of an Investigational mRNA Vaccine for the Prevention of Respiratory Syncytial Virus and/or Human Metapneumovirus in Participants Aged 18 to 49 Years and 60 Years and Older

NCT04491877Phase 1CompletedPrimary

Study of an Live-Attenuated Respiratory Syncytial Virus Vaccine in Infants and Toddlers

NCT06904222Phase 1Active Not RecruitingPrimary

Safety and Immunogenicity of the Recombinant Respiratory Syncytial Virus (RSV) Vaccine in Adults Aged 18 Years and Older

NCT06206720Phase 2CompletedPrimary

A Study of Deuremidevir Hydrobromide for Suspension in Chinese Infants Hospitalized With RSV

NCT05987072Phase 1CompletedPrimary

A Study to Learn How the Study Medicine Called Sisunatovir is Tolerated and Acts in the Bodies of Chinese Healthy Adults.

NCT06424795CompletedPrimary

Molecular and Microbiome/Metagenome Correlates of Recurrent Wheeze in RSV Infected Infants

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