Key Insights

Highlights

Success Rate

95% trial completion (above average)

Published Results

28 trials with published results (41%)

Research Maturity

54 completed trials (79% 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

94.7%

+8.2% vs benchmark

Late-Stage Pipeline

66%

45 trials in Phase 3/4

Results Transparency

52%

28 of 54 completed with results

Key Signals

28 with results95% success

Data Visualizations

Phase Distribution

58Total
Not Applicable (2)
P 1 (3)
P 2 (8)
P 3 (31)
P 4 (14)

Trial Status

Completed54
Unknown6
Not Yet Recruiting3
Terminated3
Withdrawn1
Recruiting1

Trial Success Rate

94.7%

Benchmark: 86.5%

Based on 54 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

NCT06331702Phase 4Completed

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

NCT07112846Not Yet Recruiting

Prospective Clinical Registry for Evaluation of Exanthematous Infections and Coinfections

NCT03071575Phase 4Completed

Measles-Rubella Vaccine Immunogenicity at 6 and 9 Months of Age

NCT06815835Phase 3Not Yet Recruiting

Non-interference Study of MR and Yellow Fever Vaccines Among Bangladeshi Infants Aged 9-12 Months

NCT05894395Phase 3Unknown

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

NCT05771779Phase 3Unknown

Co-administration Study of OCV, TCV and MR

NCT05952505Phase 4Unknown

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

NCT04394689Phase 1Completed

Measles and Rubella Vaccine Microneedle Patch Phase 1-2 Age De-escalation Trial

NCT05279248Phase 4Unknown

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

NCT00962819Completed

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

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

NCT03148990Phase 2CompletedPrimary

Study to Evaluate the Immunogenicity, Reatogenicity and Safety of Double Viral Vaccine (MR) for Measles and Rubella

NCT00861744Phase 2CompletedPrimary

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

NCT01702428Phase 3CompletedPrimary

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

NCT00092430Phase 3Completed

Study to Evaluate Frozen Versus Refrigerated MMRV (Combined Measles, Mumps, Rubella, and Varicella) Investigational Vaccine (V221-016)

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