Success Metrics

Clinical Success Rate
93.5%

Based on 29 completed trials

Completion Rate
94%(29/31)
Active Trials
0(0%)
Results Posted
66%(19 trials)
Terminated
2(6%)

Phase Distribution

Ph phase_3
13
41%
Ph phase_4
8
25%
Ph phase_1
2
6%
Ph phase_2
4
13%

Phase Distribution

2

Early Stage

4

Mid Stage

21

Late Stage

Phase Distribution27 total trials
Phase 1Safety & dosage
2(7.4%)
Phase 2Efficacy & side effects
4(14.8%)
Phase 3Large-scale testing
13(48.1%)
Phase 4Post-market surveillance
8(29.6%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

90.6%

29 of 32 finished

Non-Completion Rate

9.4%

3 ended early

Currently Active

0

trials recruiting

Total Trials

32

all time

Status Distribution
Completed(29)
Terminated(3)

Detailed Status

Completed29
Terminated2
Withdrawn1

Development Timeline

Analytics

Development Status

Total Trials
32
Active
0
Success Rate
93.5%
Most Advanced
Phase 4

Trials by Phase

Phase 12 (7.4%)
Phase 24 (14.8%)
Phase 313 (48.1%)
Phase 48 (29.6%)

Trials by Status

terminated26%
withdrawn13%
completed2991%

Recent Activity

Clinical Trials (32)

Showing 20 of 32 trialsScroll for more
NCT04301154Phase 1

Safety and Effects of Using Prime-boost HIVIS DNA and MVA-CMDR Vaccine Regimens With or Without Toll-like Receptor 4 Agonist on HIV Reservoirs in Perinatally HIV Infected Children and Youth

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
NCT00481767Phase 3

Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Human Papillomavirus (HPV) Vaccine (GSK580299) in Healthy Female Subjects 10-25 Years of Age.

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
NCT01627561Phase 3

Safety and Immunogenicity of GSK Biologicals' HPV-16/18 L1 VLP AS04 Vaccine (GSK-580299) in Healthy Female Children 4-6 Years Old

Completed
NCT00586339Phase 2

Safety and Immunogenicity of GlaxoSmithKline Biologicals' HPV Vaccine 580299 (Cervarix) in HIV Infected Females

Completed
NCT00294047Phase 3

Study to Evaluate the Efficacy of the Human Papillomavirus Vaccine in Healthy Adult Women of 26 Years of Age and Older

Completed
NCT00250276Phase 3

Evaluation of the Immune Responses of GSK Biologicals' HPV Vaccine Following Manufacturing Process Adaptation.

Completed
NCT00196937Phase 3

Human Papilloma Virus (HPV) Vaccine Immunogenicity and Safety Trial in Young and Adult Women With GSK Biologicals' HPV-16/18

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
NCT00534638Phase 4

Effectiveness, Safety and Immunogenicity of GSK Biologicals' HPV Vaccine GSK580299 (Cervarix) Administered in Healthy Adolescents

Completed
NCT00730847Phase 4

A Study to Assess the Safety and Reactogenicity of GlaxoSmithKline (GSK) Biologicals' Human Papillomavirus (HPV) Vaccine (Cervarix) in Healthy Female Filipino Subjects Vaccinated According to the Prescribing Information From the Age of 10 Years Onwards.

Terminated
NCT01190176Phase 3

Gynaecological Follow-up of a Subset of HPV-015 (NCT00294047) Study Subjects

Completed
NCT02837926Phase 4

Comparing Health Services Interventions for the Prevention of HPV-related Cancer

Completed
NCT00122681Phase 3

Human Papilloma Virus (HPV) Vaccine Efficacy Trial Against Cervical Pre-cancer in Young Adults With GlaxoSmithKline (GSK) Biologicals HPV-16/18

Completed
NCT00578227Phase 3

Evaluation of Safety and Immunogenicity of Co-administering Human Papillomavirus Vaccine With Another Vaccine in Healthy Female Subjects

Completed
NCT00541970Phase 1

Partially Blind Study to Evaluate Immunogenicity & Safety of GSK Bio's HPV Vaccine 580299 in Healthy Women Aged 9-25 Yrs

Completed
NCT01101542

Evaluation of Safety of a Vaccine Against Cervical Cancer in Healthy Korean Females

Completed
NCT01755689Phase 3

Immunogenicity and Safety Study of GlaxoSmithKline (GSK) Biologicals' Meningococcal Vaccine With or Without Co-administration of Cervarix and Boostrix in Female Adolescents and Young Adults

Completed

Drug Details

Intervention Type
BIOLOGICAL
Total Trials
32