Key Insights

Highlights

Success Rate

92% trial completion (above average)

Published Results

11 trials with published results (42%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

7.7%

2 terminated out of 26 trials

Success Rate

91.7%

+5.2% vs benchmark

Late-Stage Pipeline

35%

9 trials in Phase 3/4

Results Transparency

50%

11 of 22 completed with results

Key Signals

11 with results92% success

Data Visualizations

Phase Distribution

22Total
Not Applicable (3)
P 1 (2)
P 2 (8)
P 3 (4)
P 4 (5)

Trial Status

Completed22
Terminated2
Recruiting1
Unknown1

Trial Success Rate

91.7%

Benchmark: 86.5%

Based on 22 completed trials

Clinical Trials (26)

Showing 20 of 20 trials
NCT04682444Phase 2Completed

Efficacy and Safety of Enisamium Iodide for the Treatment of Acute Respiratory Viral Infections, Including Influenza.

NCT04487041Phase 4RecruitingPrimary

Tfh Dysfunction in HIV and Aging

NCT04431050TerminatedPrimary

Evaluation of a Single Use Point of Care Device for the Diagnosis of Respiratory Pathogens

NCT05155319Phase 1CompletedPrimary

Universal Influenza A Vaccine in Healthy Adults

NCT01342796Phase 2Completed

Humoral and Cell Mediated Immunity and Safety of MF59C.1-adjuvanted Subunit Influenza Vaccine or a Conventional Subunit Influenza Vaccine in Previously Unvaccinated Healthy Subjects

NCT02387294Phase 3CompletedPrimary

Immunogenicity and Tolerability Study of Fluval AB Novo Suspension for Injection for Children and Adolescents

NCT03448705Phase 1CompletedPrimary

Safety of 4Fluart ID Suspension for Injection in Adult Subjects

NCT03572491Phase 3CompletedPrimary

Preventive Effectiveness, Safety and Immunogenicity of a Allantoic Split Inactivated Seasonal Influenza Vaccine

NCT02478905CompletedPrimary

Transmission of Influenza Virus From Asymptomatic Healthcare Workers and Inpatients in the Acute Care Hospital Setting

NCT02600585CompletedPrimary

Post-Marketing Observational Study of Safety Following Vaccination With Flublok® Compared to Licensed IIV in Adults

NCT01880697Phase 3CompletedPrimary

Safety and Immunogenicity of a Cell Derived Subunit Trivalent Nonadjuvanted Influenza Study Vaccine in Adults Aged 18 Years and Above

NCT01636102Phase 2CompletedPrimary

Safety and Immunogenicity of a Subunit Trivalent Nonadjuvated Influenza Study Vaccine in Adults Aged 18 Years and Above

NCT02427750Phase 2CompletedPrimary

A Study to Evaluate Safety and Immunogenicity of Trivalent Influenza Vaccine, Formulation 2015 Southern Hemisphere, When Administered to Healthy Adult Subjects.

NCT02104869Phase 4CompletedPrimary

Clinical Trial for the Evaluation of Three Regimens of Influenza Vaccination in Kidney Transplant Recipients

NCT02398097Phase 4CompletedPrimary

Conventional Vaccine and Intradermal Vaccine Among HIV-infected Young Subjects

NCT01690637Phase 4Terminated

Panama and El Salvador Children's Oseltamivir Study

NCT01651104Phase 2CompletedPrimary

Safety and Immunogenicity of a Trivalent Influenza Vaccine When Administered to Elderly Subjects

NCT01879540Phase 2CompletedPrimary

Safety and Immunogenicity of a Subunit Trivalent Influenza Vaccine, Northern Hemisphere Formulation 2013/2014, Including MF59C.1 Adjuvant, in Healthy Adults ≥65 Years of Age

NCT01879553Phase 2CompletedPrimary

Safety and Immunogenicity of a Subunit Trivalent Influenza Vaccine, Northern Hemisphere Formulation 2013/2014, in Healthy Adults Aged 18 Years and Above

NCT01885117Phase 3CompletedPrimary

Safety and Immunogenicity of One Dose of Seasonal Trivalent Influenza Virus Vaccine (TIVf, Purified Surface Antigen, Inactivated, Egg Derived) in Adults, Aged 18 Years and Above

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