Key Insights

Highlights

Success Rate

94% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

3.8%

1 terminated out of 26 trials

Success Rate

94.4%

+7.9% vs benchmark

Late-Stage Pipeline

31%

8 trials in Phase 3/4

Results Transparency

53%

9 of 17 completed with results

Key Signals

9 with results94% success

Data Visualizations

Phase Distribution

19Total
Not Applicable (2)
P 1 (5)
P 2 (4)
P 3 (7)
P 4 (1)

Trial Status

Completed17
Unknown5
Active Not Recruiting2
Terminated1
Withdrawn1

Trial Success Rate

94.4%

Benchmark: 86.5%

Based on 17 completed trials

Clinical Trials (26)

Showing 20 of 20 trials
NCT06485258Phase 1CompletedPrimary

CDC-9 Inactivated Rotavirus Vaccine (IRV) Intramuscular (IM) Phase 1 Clinical Trial in Healthy Adults

NCT06962904Phase 1Active Not RecruitingPrimary

CDC-9 Inactivated Rotavirus Vaccine (IRV) Microneedle Patch (MNP) in Healthy Adults

NCT03313128CompletedPrimary

SaniVac Trial - Sanitation and Oral Rotavirus Vaccine Performance

NCT05621655Phase 2Active Not RecruitingPrimary

Safety and Immunogenicity Study of Recombinant Trivalent Rotavirus Subunit Vaccine in Healthy Infants and Toddlers

NCT06080906Phase 2UnknownPrimary

Phase II Clinical Trial of the Inactivated Rotavirus Vaccine

NCT03483116Phase 2CompletedPrimary

A Phase II Dose-ranging Study of Oral RV3-BB Rotavirus Vaccine

NCT05212935Unknown

A Surveillance Study on Timing and Coverage Of Rotavirus and MenB Vaccine Co-administration in Campania Region, Italy

NCT05037435Phase 3CompletedPrimary

Safety and Immunological Efficacy of the Pentavalent Rotavirus Vaccine - Rota-V-Aid™ (Live Attenuated Oral, Freeze-dried) at Healthy Adults Aged 18 to 45 Years.

NCT03870061Not ApplicableCompleted

Evaluation of an Infant Immunization Encouragement Program in Nigeria

NCT03367559Phase 3UnknownPrimary

Evaluate Immunogenicity, Safety, and Reactogenicity of Rotavac® in Healthy Infants Aged Between 6-8 Weeks in Vietnam

NCT02542462Phase 4Completed

Potential Mechanisms for Intussusception After Rotavirus Vaccine-Pilot Study

NCT00443846Phase 3Completed

RotaTeq® and Meningococcus C Vaccine in Healthy Infants (V260-016)

NCT02538211Not ApplicableCompletedPrimary

The Role of the Intestinal Microbiome in Enteric and Systemic Vaccine Immune Responses

NCT00346892Phase 2CompletedPrimary

To Evaluate 2 Doses of GSK Biologicals' Oral Live Attenuated Human HRV Vaccine Co-administered With Either OPV or IPV

NCT01467037CompletedPrimary

Vaccine Effectiveness of RV1 in a Naïve Population

NCT01357174TerminatedPrimary

ROTATEQ™ Post-Marketing Surveillance in the Philippines

NCT00092456Phase 3CompletedPrimary

Consistency Lots Vaccine Study (V260-009)

NCT00090233Phase 3CompletedPrimary

Rotavirus Efficacy and Safety Trial (REST)(V260-006)

NCT00092443Phase 3CompletedPrimary

Dose Confirmation Efficacy Study (V260-007)

NCT00130832Phase 3CompletedPrimary

Concomitant Use and Staggered Use of Vaccine and Oral Poliovirus (OPV) in Healthy Infants (V260-014)(COMPLETED)

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