Key Insights

Highlights

Success Rate

91% trial completion (above average)

Published Results

15 trials with published results (34%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

6.8%

3 terminated out of 44 trials

Success Rate

90.6%

+4.1% vs benchmark

Late-Stage Pipeline

16%

7 trials in Phase 3/4

Results Transparency

52%

15 of 29 completed with results

Key Signals

15 with results91% success

Data Visualizations

Phase Distribution

33Total
Not Applicable (4)
P 1 (11)
P 2 (11)
P 3 (7)

Trial Status

Completed29
Active Not Recruiting7
Recruiting3
Terminated3
Unknown2

Trial Success Rate

90.6%

Benchmark: 86.5%

Based on 29 completed trials

Clinical Trials (44)

Showing 20 of 20 trials
NCT07117487Phase 3CompletedPrimary

A Study of mRNA-1345 Following a Primary Dose of a Licensed Protein Subunit Respiratory Syncytial Virus (RSV) Vaccine in Adult Participants ≥60 Years of Age

NCT05397223Phase 1Completed

A Study of Modified mRNA Vaccines in Healthy Adults

NCT06593587Phase 3CompletedPrimary

A Study to Assess the Safety, Tolerability, and Immunogenicity of RSVpreF in Older Adults in Korea

NCT06143046Phase 2Active Not RecruitingPrimary

A Study of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus in Pregnant Women and in Infants Born to Vaccinated Mothers

NCT05330975Phase 3CompletedPrimary

A Study of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in Adults ≥50 Years of Age

NCT07289503Phase 1Active Not RecruitingPrimary

Phase I Clinical Trial of Lyophilized Respiratory Syncytial Virus mRNA Vaccine in Adults Aged 18 Years or Above

NCT07289542Phase 2Active Not RecruitingPrimary

Phase II Clinical Trial of Lyophilized Respiratory Syncytial Virus mRNA Vaccine in Adults Aged 50 Years or Above

NCT07200206RecruitingPrimary

A Post-marketing Surveillance Study of Beyfortus (Nirsevimab) in Republic of Korea

NCT05743881Phase 1Active Not RecruitingPrimary

A Safety, Tolerability, and Immunogenicity Study of mRNA-1345 and mRNA-1365 in Participants Aged 5 Months to <24 Months

NCT07122661Active Not Recruiting

STudy of Real World vaccinE Effectiveness of maTernal RSVpreF vaccinatiON Against Respiratory Syncytial Virus (RSV) in Hospitalised Infants in Australia (STREETON)

NCT06325332CompletedPrimary

BEYFORTUS™ (Nirsevimab) Effectiveness Against Medically-Attended RSV Events in Infants (BEAR Study)

NCT06647654Active Not RecruitingPrimary

Impact and Effectiveness of ABRYSVO® Vaccination During Pregnancy

NCT05127434Phase 2CompletedPrimary

A Study to Evaluate the Safety and Efficacy of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in Adults ≥60 Years of Age

NCT06067230Phase 3Active Not RecruitingPrimary

A Study to Investigate the Immunogenicity and Safety of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in High-risk Adults

NCT06060457Phase 3CompletedPrimary

A Study to Evaluate the Safety and Immune Response of mRNA-1345, a Vaccine Targeting Respiratory Syncytial Virus (RSV), When Co-administered With a Fluzone HD, in Adults ≥65 Years of Age

NCT05559905Phase 2CompletedPrimary

Respiratory Syncytial Virus (RSV) Human Challenge Study of Molnupiravir in Healthy Participants (MK-4482-017)

NCT06325657Phase 3CompletedPrimary

A Study to Learn About the Vaccine RSVpreF In Pregnant Participants With HIV and Their Infants

NCT06097299Phase 2CompletedPrimary

A Study of mRNA-1345, an mRNA Vaccine Targeting Respiratory Syncytial Virus, in Children 2 to <18 Years of Age at High Risk of Respiratory Syncytial Virus

NCT06488300Phase 2RecruitingPrimary

Assessing Antiviral Treatments in Early Symptomatic RSV

NCT06754605Phase 1RecruitingPrimary

A Study to Evaluate the Safety, Tolerability, and Immunogenicity of a Recombinant Respiratory Syncytial Virus Vaccine

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