Key Insights

Highlights

Success Rate

100% trial completion (above average)

Published Results

20 trials with published results (34%)

Research Maturity

56 completed trials (97% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

0.0%

0 terminated out of 58 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

41%

24 trials in Phase 3/4

Results Transparency

36%

20 of 56 completed with results

Key Signals

20 with results100% success

Data Visualizations

Phase Distribution

36Total
P 1 (3)
P 2 (9)
P 3 (22)
P 4 (2)

Trial Status

Completed56
Withdrawn2

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 56 completed trials

Clinical Trials (58)

Showing 20 of 20 trials
NCT03954743Phase 3CompletedPrimary

Safety Study of 2 Formulations of GSK's Human Rotavirus (HRV) Vaccine (444563), in Healthy Infants Starting at Age 6-12 Weeks

NCT00353366CompletedPrimary

To Evaluate Safety & Reactogenicity of GSK Bio's Human Rotavirus (HRV) Vaccine in Filipino Infants at Least 6 Weeks of Age at First Vaccination

NCT00263666Phase 2CompletedPrimary

A Study of Safety, Reactogenicity and Immunogenicity of HRV Vaccine in HIV Infected Infants in South Africa

NCT02914184Phase 3CompletedPrimary

Evaluation of Immunogenicity and Safety of Two Formulations of GSK Biologicals' Human Rotavirus (HRV) Vaccine (444563), in Healthy Infants Starting at Age 6-12 Weeks

NCT00750893CompletedPrimary

Evaluation of Reactogenicity and Safety of GSK Biologicals' Rotarix (Human Rotavirus Vaccine) in Infants

NCT00969228Phase 4CompletedPrimary

Study to Evaluate Immunogenicity, Reactogenicity and Safety of Rotarix™ Vaccine in Korean Infants

NCT01177826CompletedPrimary

Effectiveness Study of GSK Biologicals' Rotarix TM Vaccine in Hospitalized Children

NCT00432380Phase 2CompletedPrimary

A Study to Evaluate Immune Response and Safety of Two Doses of GSK Biologicals' HRV Liquid Vaccine in Healthy Infants.

NCT00480324Phase 3CompletedPrimary

Efficacy, Safety, Reactogenicity & Immunogenicity of the Rotarix Vaccine in Japanese Infants

NCT00140673Phase 3CompletedPrimary

A Study to Test 2 Doses of the HRV Vaccine in Healthy Infants.

NCT00385320Phase 2CompletedPrimary

Evaluate Protective Efficacy of Diff Strengths of Human Rotavirus Vaccine After Admn of 2 Doses to Infants Aged 2 Months

NCT01733862CompletedPrimary

Study to Assess the Impact of Vaccination on Hospitalizations and Outpatient Visits Due to Rotavirus Gastroenteritis

NCT00875641CompletedPrimary

Safety Study of GSK Biologicals' Rotavirus Vaccine (Rotarix®) Administered to Children Aged <1 Year in the United States

NCT00779779CompletedPrimary

Evaluation of Reactogenicity and Safety of GSK Biologicals' Rotarix™ (Human Rotavirus Vaccine) in Infants

NCT00420316Phase 3CompletedPrimary

Long-term Efficacy and Safety of Subjects Approximately 3 Years After Priming With 2 Doses of GSK Bio's HRV Vaccine.

NCT01198769Phase 4CompletedPrimary

Immunogenicity and Safety Study of Rotarix TM in Taiwanese Infants Who Received Hepatitis B Immunoglobulin After Birth.

NCT01171963Phase 3CompletedPrimary

Study to Assess the Efficacy, Immunogenicity and Safety of Liquid Human Rotavirus Vaccine, in Healthy Chinese Infants

NCT00420745Phase 3CompletedPrimary

To Assess Safety, Reactogenicity & Immunogenicity of 2 Doses of GSK's Oral Human Rotavirus Vaccine in Pre-Term Infants

NCT00533507Phase 3CompletedPrimary

Primary Vaccination Study With a Pneumococcal Conjugate Vaccine in Healthy Children 6 to 8 Weeks of Age

NCT00363545Phase 3CompletedPrimary

To Assess Immunogenicity, Reactogenicity & Safety of 2 Formulations of GSK's HRV Vaccine as 2-dose Vaccination (Infants)

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