Key Insights

Highlights

Success Rate

95% trial completion (above average)

Published Results

27 trials with published results (40%)

Research Maturity

55 completed trials (81% of total)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

4.4%

3 terminated out of 68 trials

Success Rate

94.8%

+8.3% vs benchmark

Late-Stage Pipeline

68%

46 trials in Phase 3/4

Results Transparency

49%

27 of 55 completed with results

Key Signals

27 with results95% success

Data Visualizations

Phase Distribution

58Total
Not Applicable (2)
P 1 (3)
P 2 (7)
P 3 (32)
P 4 (14)

Trial Status

Completed55
Unknown6
Terminated3
Active Not Recruiting1
Recruiting1
Not Yet Recruiting1

Trial Success Rate

94.8%

Benchmark: 86.5%

Based on 55 completed trials

Clinical Trials (68)

Showing 20 of 20 trials
NCT02325310Phase 4Completed

Search for the Measles Vaccine Virus Excretion in Breast Milk of Breastfeeding Women After Postpartum Vaccination With MMR

NCT07358910Recruiting

Risk Assessment of Community Spread of Multiple Endemic Infectious Diseases in a One Health Perspective

NCT07338851Not Yet Recruiting

the Five-year Antibody Persistence After Immunization With IPV, MMR and HepA-L Vaccines

NCT06967181Phase 1Active Not RecruitingPrimary

A Phase 1 Trial of Intranasal Mumps Virus Vaccines in Healthy Adults

NCT06331702Phase 4Completed

Immunogenicity of Japanese Encephalitis Vaccine Co-administered With Measles-Mumps-Rubella Vaccine (MMR)

NCT06208683Phase 4UnknownPrimary

The Immunogenicity and Safety of the Booster Doses of a Live-attenuated Mumps Vaccine in Junior High School Students

NCT05894395Phase 3UnknownPrimary

Immunity in Persons Fully Vaccinated Against Measles, Mumps and Rubella and Responses to Booster Vaccination

NCT01712906Phase 1CompletedPrimary

A Phase I, Safety Study of Live Attenuated Mumps (F-genotype) Vaccine (Human Diploid Cell, KMB-17) in Chinese Children

NCT05952505Phase 4Unknown

Immunogenicity and Safety of an Inactivated SARS-CoV-2 Vaccine Coadministered With Two Attenuated Vaccines

NCT05279248Phase 4Unknown

The Immunogenicity and Safety of the Vaccination of Human Papillomavirus Vaccine and Measles-Mumps-Rubella Vaccine

NCT05145166CompletedPrimary

Safety Study of Live Attenuated Mumps Vaccines in Junior High School Students Under 14 Years Old

NCT00432523Phase 3Completed

Immunogenicity and Safety of Concomitant Administration of MMR™ rHA and VARIVAX® by Intramuscular Versus Subcutaneous Route (V205C-011)

NCT00962819Completed

Measles, Mumps, and Rubella (MMR) Immunity in College Students

NCT05065177Phase 3CompletedPrimary

Safety and Immunogenicity Study of Live Attenuated Mumps Vaccines in Healthy Infants

NCT04364399Phase 4CompletedPrimary

Clinical Trial to Evaluate the Safety and Immunogenicity of Mumps Vaccine

NCT01681992Phase 3Completed

Immunogenicity and Safety Study of GlaxoSmithKline (GSK) Biologicals' Combined Measles-mumps-rubella (MMR) Vaccine in Children in Their Second Year of Life

NCT02880865Phase 4Completed

Immunogenicity and Safety of Japanese Encephalitis Vaccine When Given With Measles-Mumps-Rubella (MMR) Vaccine

NCT00861744Phase 2Completed

Immunogenicity of GSKs' MMR Vaccine (209762) vs. M-M-R® II, When Given With Routine Vaccines at 12-15 Months of Age

NCT01702428Phase 3Completed

Consistency Study of GlaxoSmithKline (GSK) Biologicals' MMR Vaccine (209762) (Priorix) Comparing Immunogenicity and Safety to Merck & Co., Inc.'s MMR Vaccine (M-M-R II), in Children 12 to 15 Months of Age

NCT00892775Phase 2Completed

Immunogenicity & Safety Study of GSK Biologicals' 208136 Vaccine Formulated With New Measles and Rubella Working Seeds

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