Key Insights

Highlights

Success Rate

97% trial completion (above average)

Published Results

45 trials with published results (69%)

Research Maturity

61 completed trials (94% of total)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 5/100

Termination Rate

3.1%

2 terminated out of 65 trials

Success Rate

96.8%

+10.3% vs benchmark

Late-Stage Pipeline

63%

41 trials in Phase 3/4

Results Transparency

74%

45 of 61 completed with results

Key Signals

45 with results97% success

Data Visualizations

Phase Distribution

55Total
P 1 (3)
P 2 (11)
P 3 (39)
P 4 (2)

Trial Status

Completed61
Withdrawn2
Terminated2

Trial Success Rate

96.8%

Benchmark: 86.5%

Based on 61 completed trials

Clinical Trials (65)

Showing 20 of 20 trials
NCT00947115Phase 3CompletedPrimary

Evaluation of Long-term Immunogenicity and Safety of a Human Papillomavirus (HPV) Vaccine in Healthy Female Subjects

NCT01031069Phase 4CompletedPrimary

Evaluation of Safety and Immunogenicity of a Human Papillomavirus (HPV) Vaccine in Human Immunodeficiency Virus (HIV) Infected Females

NCT01381575Phase 3CompletedPrimary

Evaluation of Immunogenicity and Safety of Two 2-dose Human Papillomavirus (HPV) Vaccine Schedules in 9-14 Year Old Girls

NCT01627561Phase 3CompletedPrimary

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

NCT00877877Phase 3CompletedPrimary

Evaluation of Long-term Immunogenicity and Safety of a Human Papillomavirus (HPV) Vaccine in Healthy Female Subjects.

NCT00586339Phase 2CompletedPrimary

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

NCT00637195Phase 3CompletedPrimary

Immunogenicity and Safety of a Commercially Available Vaccine Co-administered With GSK HPV Vaccine (580299)

NCT00294047Phase 3CompletedPrimary

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

NCT00250276Phase 3CompletedPrimary

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

NCT00359619Phase 2CompletedPrimary

Human Papillomavirus Vaccine Immunogenicity and Safety Trial in Young Adult Women With GSK Biologicals Novel HPV Vaccine

NCT00423046Phase 3CompletedPrimary

Immunogenicity of GlaxoSmithKline Biological's Human Papillomavirus (HPV) Vaccine (580299) Versus Merck's Gardasil® in Healthy Females 18-45 Years of Age

NCT00231413Phase 2CompletedPrimary

Human Papilloma Virus Vaccine Immunogenicity and Safety Trial in Young Adult Women With GSK Bio's Novel HPV Vaccine.

NCT00196937Phase 3CompletedPrimary

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

NCT01462357Phase 3CompletedPrimary

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

NCT00534638Phase 4CompletedPrimary

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

NCT01249365Phase 3CompletedPrimary

The Safety Evaluation of the GSK-580299 Vaccine in Women From the Control Group in the Primary NCT00294047 Study

NCT01190176Phase 3CompletedPrimary

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

NCT00937950Phase 3CompletedPrimary

Gynaecological Follow-up of a Subset of 580299/008 (NCT00122681) Study Subjects

NCT01190189Phase 3CompletedPrimary

Safety Evaluation of the GSK-580299 Vaccine in Women From the Control Group in the Primary NCT00294047 Study

NCT00779766Phase 3CompletedPrimary

Efficacy, Immunogenicity and Safety of GSK Biologicals' HPV GSK 580299 Vaccine in Healthy Chinese Female Subjects

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