Success Metrics

Clinical Success Rate
95.5%

Based on 21 completed trials

Completion Rate
95%(21/22)
Active Trials
3(9%)
Results Posted
62%(13 trials)
Terminated
1(3%)

Phase Distribution

Ph phase_2
5
16%
Ph phase_3
8
25%
Ph phase_4
6
19%
Ph not_applicable
3
9%
Ph phase_1
6
19%

Phase Distribution

6

Early Stage

5

Mid Stage

14

Late Stage

Phase Distribution28 total trials
Phase 1Safety & dosage
6(21.4%)
Phase 2Efficacy & side effects
5(17.9%)
Phase 3Large-scale testing
8(28.6%)
Phase 4Post-market surveillance
6(21.4%)
N/ANon-phased studies
3(10.7%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

87.5%

21 of 24 finished

Non-Completion Rate

12.5%

3 ended early

Currently Active

3

trials recruiting

Total Trials

32

all time

Status Distribution
Active(3)
Completed(21)
Terminated(3)
Other(5)

Detailed Status

Completed21
unknown5
Withdrawn2
Active, not recruiting2
Terminated1
Recruiting1

Development Timeline

Analytics

Development Status

Total Trials
32
Active
3
Success Rate
95.5%
Most Advanced
Phase 4

Trials by Phase

Phase 16 (21.4%)
Phase 25 (17.9%)
Phase 38 (28.6%)
Phase 46 (21.4%)
N/A3 (10.7%)

Trials by Status

terminated13%
withdrawn26%
recruiting13%
active_not_recruiting26%
unknown516%
completed2166%

Recent Activity

Clinical Trials (32)

Showing 20 of 32 trialsScroll for more
NCT04508309Phase 3

Phase 3 Trial of a Bivalent Human Papilloma Virus (HPV) Vaccine (Cecolin®) in Young Girls

Completed
NCT00798265Phase 1

A Phase I Study of Quadrivalent Human Papilloma Virus (HPV) (Types 6, 11, 16, 18) Recombinant Vaccine in HIV-Infected and HIV-Negative Pre-Adolescents, Adolescents, and Young Adults

Terminated
NCT02653118

Long-term Follow-up of Broad Spectrum Human Papillomavirus (HPV) Vaccine Study in Women (V503-021)

Active Not Recruiting
NCT04422366Phase 3

Evaluate the Efficacy, Immunogenicity and Safety of 9-valent HPV Recombinant Vaccine in Chinese Healthy Females

Recruiting
NCT06142461Phase 2

Safety and Immunogenicity of HPV Vaccine Administered Intradermally and Intramuscularly Via Needle-Free Injection System

Withdrawn
NCT00513526Phase 2

Human Papillomavirus Vaccine Therapy in Treating Men With HIV-1 Infection

Completed
NCT01914367Phase 4

Study of the Molecular Mechanisms Underlying the Cross-neutralizing Capacity of AS04-adjuvanted HPV Vaccine (Cervarix®) in Comparison With the Aluminiumhydroxyphosphate Sulphate Adjuvanted HPV Vaccine (Gardasil®)

Completed
NCT03998254Phase 3

Efficacy, Immunogenicity and Safety of V503 in Chinese Women Aged 20-45 Years (V503-023)

Active Not Recruiting
NCT04425291Phase 3

Evaluate the Immunogenicity and Safety of 4-valent and 9-valent HPV Recombinant Vaccine in Chinese Healthy Females

Completed
NCT05060484Phase 2

A Phase II Study of SCT1000 in Healthy Women Aged 18 to 45 Years

Unknown
NCT04453241Phase 1

Immunogenicity and Safety Study of NBP615 in Healthy Female

Completed
NCT04921111Phase 1

A Phase I Safty and Immunogenicity Study of SCT1000 in Healthy Women Aged 18 to 45 Years

Unknown
NCT01432574Phase 2

Study of Gardasil in Mid-Adult Males (MAM)

Completed
NCT02087384Phase 4

HPV (Human Papilloma Virus) Vaccination After Treatment of Anal Intraepithelial Neoplasia (AIN)

Completed
NCT00956553Phase 4

Reactogenicity Study of Cervarix and Gardasil in UK Adolescent Girls

Completed
NCT03105856Phase 4

FASTER-Tlalpan Study in Mexico: HPV Vaccination Impact on Cervical Cancer Screening Program

Completed
NCT01462357Phase 3

Immunogenicity and Safety Study of GlaxoSmithKline Biologicals' Human Papillomavirus (HPV) Vaccine (GSK-580299) and Merck's Gardasil Vaccine When Administered According to Alternative 2-dose Schedules in 9-14 Year Old Females

Completed
NCT01092195Phase 1

Gardasil Vaccination in Post Stem Cell Transplant Patients

Completed
NCT04022148

The Prospective Cohort Study to Evaluate the Preventive Efficacy of HPV Vaccine in Japanese Women Aged 27-45 Years

Unknown
NCT01461993Phase 2

A Clinical Trial to Study the Safety, Tolerance and Immunogenic Response to Gardasil and Bivalent rLP2086 Vaccine When Given at the Same Time to Children Between the Ages of 11 and 17

Completed

Drug Details

Intervention Type
BIOLOGICAL
Total Trials
32