Success Metrics

Clinical Success Rate
100.0%

Based on 14 completed trials

Completion Rate
100%(14/14)
Active Trials
3(18%)
Results Posted
79%(11 trials)

Phase Distribution

Ph phase_3
13
76%
Ph phase_1
1
6%
Ph phase_2
1
6%
Ph phase_4
2
12%

Phase Distribution

1

Early Stage

1

Mid Stage

15

Late Stage

Phase Distribution17 total trials
Phase 1Safety & dosage
1(5.9%)
Phase 2Efficacy & side effects
1(5.9%)
Phase 3Large-scale testing
13(76.5%)
Phase 4Post-market surveillance
2(11.8%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

100.0%

14 of 14 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

3

trials recruiting

Total Trials

17

all time

Status Distribution
Active(3)
Completed(14)

Detailed Status

Completed14
Active, not recruiting3

Development Timeline

Analytics

Development Status

Total Trials
17
Active
3
Success Rate
100.0%
Most Advanced
Phase 4

Trials by Phase

Phase 11 (5.9%)
Phase 21 (5.9%)
Phase 313 (76.5%)
Phase 42 (11.8%)

Trials by Status

completed1482%
active_not_recruiting318%

Recent Activity

Clinical Trials (17)

Showing 17 of 17 trials
NCT06736041Phase 3

Study of a 4-Dose Regimen of a 21-valent Pneumococcal Conjugate Vaccine in Healthy Infants From Approximately 2 Months of Age

Active Not Recruiting
NCT06824194Phase 3

Study of the Safety of a 21-valent Pneumococcal Conjugate Vaccine in Healthy Infants From Approximately 2 Months of Age

Active Not Recruiting
NCT06824181Phase 3

Study of Mixed Vaccination Schedules With a 21-valent Pneumococcal Conjugate Vaccine and a 20-valent Pneumococcal Conjugate Vaccine in Healthy Infants From Approximately 2 Months of Age

Active Not Recruiting
NCT03893448Phase 3

Safety, Tolerability, and Immunogenicity of V114 in Healthy Infants (V114-029)

Completed
NCT03620162Phase 3

A Study to Evaluate the Interchangeability of V114 and Prevnar 13™ in Healthy Infants (V114-027/PNEU-DIRECTION)

Completed
NCT00880698Phase 2

Safety and Immune Response of a Rotavirus Vaccine in HIV-infected and Uninfected Children Born to HIV-infected Mothers

Completed
NCT01341639Phase 3

Safety, Tolerability, and Immunogenicity of V419 in Healthy Infants When Given at 2, 3, 4 and 12 Months (V419-007)

Completed
NCT01839188Phase 3

Spanish Mixed HEXA/PENTA/HEXA Schedule (V419-010)

Completed
NCT01337167Phase 3

Safety, Tolerability, and Immunogenicity of V419 Given Concomitantly With Prevnar 13™ and RotaTeq™ (V419-005)

Completed
NCT01340937Phase 3

A Study of V419 Given Concomitantly With Prevnar 13™ and RotaTeq™ (V419-006)

Completed
NCT02193061Phase 3

Randomized, Controlled Single-blind Clinical Study to Assess Vaccine Interchangeability Between RV5 and RV1 Using Seven Combined Anti-rotavirus Prevention Programs

Completed
NCT02542462Phase 4

Potential Mechanisms for Intussusception After Rotavirus Vaccine-Pilot Study

Completed
NCT00443846Phase 3

RotaTeq® and Meningococcus C Vaccine in Healthy Infants (V260-016)

Completed
NCT01839175Phase 3

Concomitant Administration of a New Hexavalent Vaccine With a Meningococcal Serogroup C Conjugate Vaccine in Healthy Infants During Primary Series Immunisation Followed by Booster Vaccination

Completed
NCT02728869Phase 1

Safety, Reactogenicity and Immunogenicity of Heat-stable Rotavirus Vaccine (HSRV) in Adults and Infants

Completed
NCT00090233Phase 3

Rotavirus Efficacy and Safety Trial (REST)(V260-006)

Completed
NCT01266850Phase 4

Safety and Immunogenicity of Sequential Rotavirus Vaccine Schedules

Completed

All 17 trials loaded

Drug Details

Intervention Type
BIOLOGICAL
Total Trials
17