Success Metrics

Clinical Success Rate
100.0%

Based on 5 completed trials

Completion Rate
100%(5/5)
Active Trials
5(50%)
Results Posted
100%(5 trials)

Phase Distribution

Ph phase_3
10
100%

Phase Distribution

0

Early Stage

0

Mid Stage

10

Late Stage

Phase Distribution10 total trials
Phase 3Large-scale testing
10(100.0%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

100.0%

5 of 5 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

5

trials recruiting

Total Trials

10

all time

Status Distribution
Active(5)
Completed(5)

Detailed Status

Completed5
Active, not recruiting5

Development Timeline

Analytics

Development Status

Total Trials
10
Active
5
Success Rate
100.0%
Most Advanced
Phase 3

Trials by Phase

Phase 310 (100.0%)

Trials by Status

completed550%
active_not_recruiting550%

Recent Activity

Clinical Trials (10)

Showing 10 of 10 trials
NCT05119855Phase 3

Safety and Immunogenicity of 9-valent Human Papillomavirus (9vHPV) Vaccine Coadministered With Messenger Ribonucleic Acid (mRNA)-1273 Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) (COVID-19) Vaccine (V503-076)

Completed
NCT04772534Phase 3

Immunogenicity and Safety of the 9-valent Human Papillomavirus (9vHPV) Vaccine in Japanese Boys and Girls (V503-066)

Completed
NCT04708041Phase 3

Safety and Immunogenicity of Extended 2-dose Regimens of 9-valent Human Papillomavirus (9vHPV) Vaccine (V503-069)

Active Not Recruiting
NCT04199689Phase 3

Efficacy Against Oral Persistent Infection, Immunogenicity and Safety of the 9-valent Human Papillomavirus Vaccine (9vHPV) in Men Aged 20-45 Years (V503-049)

Active Not Recruiting
NCT05285826Phase 3

Efficacy, Immunogenicity, and Safety of V503 in Chinese Males (V503-052)

Active Not Recruiting
NCT04313244Phase 3

Immunogenicity and Safety of Dengue Tetravalent Vaccine (TDV) and Recombinant 9-valent Human Papillomavirus Vaccine (9vHPV) in Participants Aged ≥9 to <15 Years

Completed
NCT05314023Phase 3

Immunogenicity and Safety of V503 in Chinese Males 9 Through 19 Years Old (V503-053)

Active Not Recruiting
NCT05450705Phase 3

V503 in Chinese Girls 9-14 Years Old Versus Chinese Women 20-26 Years Old (V503-071)

Active Not Recruiting
NCT03546842Phase 3

Safety and Immunogenicity Study of V503 (GARDASIL™9, 9vHPV Vaccine) Administered to 9- to 26-Year-Old Females and Males in Vietnam (V503-017)

Completed
NCT01651949Phase 3

Multivalent HPV (Human Papillomavirus) Vaccine Study in 16- to 26-Year Old Men and Women (V503-003)

Completed

All 10 trials loaded

Drug Details

Intervention Type
BIOLOGICAL
Total Trials
10