Key Insights

Highlights

Success Rate

100% trial completion (above average)

Published Results

17 trials with published results (77%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 5/100

Termination Rate

0.0%

0 terminated out of 22 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

50%

11 trials in Phase 3/4

Results Transparency

85%

17 of 20 completed with results

Key Signals

17 with results100% success

Data Visualizations

Phase Distribution

20Total
Not Applicable (1)
P 1 (1)
P 2 (7)
P 3 (8)
P 4 (3)

Trial Status

Completed20
Active Not Recruiting1
Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 20 completed trials

Clinical Trials (22)

Showing 20 of 20 trials
NCT07135986Phase 3Active Not RecruitingPrimary

Immunogenicity and Safety Study of an Investigational Quadrivalent Meningococcal Conjugate Vaccine Administered in Healthy Children and Adolescents in China

NCT04843111RecruitingPrimary

Observational, Passive Surveillance Program to Collect Information on Women and Their Offspring Exposed to MenQuadfi® During Pregnancy, in United States (US)

NCT06228586Phase 3CompletedPrimary

Study on a MenACYW Conjugate Vaccine Administered as a Single Dose in Participants Aged 12 Months and Older in Vietnam

NCT01890759Phase 3Completed

Immunogenicity and Safety of Menactra® Vaccine in Subjects Aged 9 to 23 Months in India and in the Russian Federation

NCT01049035Phase 2Completed

A Study of a Quadrivalent Meningococcal Tetanus Protein Conjugate Vaccine in Infants and Toddlers

NCT02531698Phase 2CompletedPrimary

A Study to Describe the Immunogenicity, Safety, and Tolerability of Neisseria Meningitidis Serogroup B Bivalent Recombinant Lipoprotein 2086 Vaccine (Bivalent rLP2086) in Healthy Subjects Aged ≥24 Months to <10 Years

NCT01543087Phase 3CompletedPrimary

Duration of hSBA Response After a Primary Series of Bivalent rLP2086 Followed by a Booster Dose

NCT01340898Phase 3CompletedPrimary

Immunogenicity and Safety Study of GSK Biologicals' Meningococcal Conjugate Vaccine When Co-administered With Routine Vaccines in Healthy Infants and Toddlers

NCT00631995Phase 1Completed

Safety and Immunogenicity of a Quadrivalent Meningococcal Tetanus Protein Conjugate Vaccine in Toddlers

NCT01689155Completed

Post-licensure Safety Surveillance Study of Menactra Vaccine When Administered As a 2-dose Schedule to Children

NCT01359449Phase 3Completed

Study of Two Doses of Menactra® or One Dose of Monovalent Meningococcal Group C Vaccine With Routine Immunizations

NCT00700635Phase 2Completed

Dose Comparison Study of Menactra® in US Children

NCT00269477Phase 2Completed

Persistence of Antibodies in Adolescents and Adults 15 to 23 Years Who Received One Dose of Menactra® or Menomune®

NCT01659996Phase 4Completed

Study of Menactra® in Healthy Subjects at 9 Months and Concomitantly With Pentacel® at 15 to 18 Months of Age

NCT01442675Phase 2Completed

Study of a Single Dose of Menactra® Vaccine 4-6 Years After Prior Menactra Vaccine

NCT00258856Phase 2Completed

Persistence of Antibodies in Children Aged 7 to 15 Years Who Previously Received One Dose of Menactra® or Menomune®

NCT00643916Phase 2Completed

Study of a Tetravalent Meningococcal Diphtheria Toxoid Conjugate Vaccine in Toddlers 9 to 18 Months of Age

NCT00392808Phase 4CompletedPrimary

Immunogenicity of the Booster Dose of Two MenC Vaccines

NCT00806195Phase 3Completed

Study to Evaluate the Safety of Novartis MenACWY Conjugate Vaccine When Administered With Routine Infant Vaccinations to Healthy Infants

NCT00715234Not ApplicableCompleted

Evaluation of Vaccination Reminder/Recall Systems for Adolescent Patients

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