Key Insights

Highlights

Success Rate

88% trial completion (above average)

Published Results

12 trials with published results (16%)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

6.7%

5 terminated out of 75 trials

Success Rate

87.8%

+1.3% vs benchmark

Late-Stage Pipeline

4%

3 trials in Phase 3/4

Results Transparency

33%

12 of 36 completed with results

Key Signals

12 with results88% success

Data Visualizations

Phase Distribution

47Total
Not Applicable (10)
P 1 (23)
P 2 (11)
P 3 (3)

Trial Status

Completed36
Unknown11
Recruiting10
Active Not Recruiting6
Terminated5
Withdrawn3

Trial Success Rate

87.8%

Benchmark: 86.5%

Based on 36 completed trials

Clinical Trials (75)

Showing 20 of 20 trials
NCT06784973Phase 2TerminatedPrimary

Study of Obeldesivir to Treat Children With Respiratory Syncytial Virus (RSV) Infection

NCT06866405Phase 3RecruitingPrimary

A Phase 3 Study of Revaccination in Subsequent Pregnancies With Bivalent RSV Vaccine and Duration of Protection of a Single Dose

NCT06984094Phase 1Active Not RecruitingPrimary

Safety and Immunogenicity Study of SCB-1022 and SCB-1033 in Healthy Older Adults

NCT04938830Phase 3CompletedPrimary

Clesrovimab (MK-1654) in Infants and Children at Increased Risk for Severe Respiratory Syncytial Virus (RSV) Disease (MK-1654-007)

NCT06640387Active Not Recruiting

CARE-ID: Dynamics of Respiratory Infections in Children and Transmission in Households and Schools

NCT04743609Not ApplicableRecruitingPrimary

RSV Burden in Outpatient and Hospital Settings

NCT07482657Phase 2Not Yet RecruitingPrimary

A Phase 2 Study to Investigate the Efficacy and Safety of Zelicapavir in Participants Aged ≥28 Days to ≤36 Months of Age Infected With Respiratory Syncytial Virus

NCT03596801Phase 1CompletedPrimary

Evaluating the Infectivity, Safety and Immunogenicity of Respiratory Syncytial Virus Vaccines, RSV 6120/∆NS1 and RSV 6120/F1/G2/∆NS1, in RSV-Seropositive Children and RSV-Seronegative Infants and Children

NCT03728413Not ApplicableCompletedPrimary

The Impact of Age on Adaptive Immunity in Adults Infected With Respiratory Syncytial Virus

NCT05765396Active Not Recruiting

SARS-CoV-2/COVID-19 Study of Next Generation Non-Invasive Passive Detection Technologies

NCT07264478Active Not RecruitingPrimary

Diagnosis and Treatment Status and Medical Burden of Respiratory Syncytial Virus Infection in Children in China

NCT06583031Phase 1CompletedPrimary

Study to Evaluate the Safety and Immune Response of an Investigational Vaccine for the Prevention of RSV (Respiratory Syncytial Virus) and (hMPV) Human Metapneumovirus Infection in Participants Aged 60 to 75 Years

NCT06170242Phase 2CompletedPrimary

A Controlled Phase 2a Study to Evaluate the Efficacy of EDP-323 Against Respiratory Syncytial Virus Infection in a Virus Challenge Model

NCT04520659Phase 1CompletedPrimary

Evaluating the Infectivity, Safety and Immunogenicity of a Recombinant Live-Attenuated Respiratory Syncytial Virus Vaccine, LID/ΔM2-2/1030s, in RSV-Seronegative Infants and Children 6 to 24 Months of Age

NCT05779995Phase 1CompletedPrimary

A Study To Evaluate the Safety of XW001 Inhalation in Children With RSV

NCT06172660RecruitingPrimary

Real-World Effectiveness of Perinatal RSV Immunoprophylaxis

NCT06585150Phase 2TerminatedPrimary

Study of Obeldesivir to Treat Nonhospitalized Adults With Acute Respiratory Syncytial Virus (RSV) Infection

NCT06601192Phase 1CompletedPrimary

A Study to Investigate the Effects of Zelicapavir (EDP-938) on QTc Interval in Healthy Adults

NCT06847464Phase 1CompletedPrimary

A Drug-Drug Interaction Study to Evaluate the Effects of Itraconazole, Carbamazepine, Quinidine and Fluconazole on the Pharmacokinetics and Safety of EDP-323.

NCT05568706Phase 2CompletedPrimary

A Study of EDP-938 in Non-hospitalized Adults With RSV Who Are at High Risk for Complications.

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