Key Insights

Highlights

Success Rate

88% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

9.5%

2 terminated out of 21 trials

Success Rate

87.5%

+1.0% vs benchmark

Late-Stage Pipeline

14%

3 trials in Phase 3/4

Results Transparency

43%

6 of 14 completed with results

Key Signals

6 with results88% success

Data Visualizations

Phase Distribution

19Total
Not Applicable (4)
P 1 (9)
P 2 (3)
P 3 (3)

Trial Status

Completed14
Recruiting2
Unknown2
Terminated2
Enrolling By Invitation1

Trial Success Rate

87.5%

Benchmark: 86.5%

Based on 14 completed trials

Clinical Trials (21)

Showing 20 of 20 trials
NCT07215871Phase 1Enrolling By InvitationPrimary

Rechallenge With a Low Pathogenicity Avian H10N7 Influenza Virus in Healthy Human Volunteers Previously Challenged With H10N7 Influenza

NCT05818124Phase 1CompletedPrimary

Efficacy and Safety of Molnupiravir in Healthy Participants Inoculated With Experimental Influenza Virus (MK-4482-019)

NCT06998264RecruitingPrimary

In-depth Analysis of the Immune Responses in the Upper Respiratory Tract of Influenza-infected Children

NCT06998251Recruiting

In-depth Analysis of the Immune Responses in the Upper Respiratory Tract in Older Adults Infected or Colonized With Streptococcus Pneumoniae (Spn)

NCT05436444Phase 1CompletedPrimary

Low Pathogenicity Avian H10N7 Influenza Virus in a Healthy Human Challenge Model

NCT04933968Phase 1Terminated

Study of ALVR106 in Patients With Respiratory Viral Infections After Hematopoietic Cell and Solid Organ Transplant

NCT03814720Phase 1CompletedPrimary

Dose, Safety, Tolerability and Immunogenicity of an Influenza H1 Stabilized Stem Ferritin Vaccine in Healthy Adults

NCT04298060Phase 2UnknownPrimary

DAS181 for Patients With Severe Hospitalized Flu and SAD-RVs (COVID-19)

NCT03784885Phase 2CompletedPrimary

A Phase 2, Double-blind Study to Evaluate Intranasal Trivalent Influenza Virus Vaccine in Healthy Adult

NCT02555618Phase 2CompletedPrimary

Phase 2 Study of TAK-850 in Comparison With Influenza Hemagglutinin (HA) Vaccine in Healthy Adult Participants

NCT02367885Phase 1CompletedPrimary

Phase 1/2 Study of TAK-850 Intramuscular Injection in Healthy Pediatric Participants

NCT02313155Phase 1CompletedPrimary

Phase 1/2 Study of TAK-850 Subcutaneous Injection in Healthy Adults

NCT00603811Phase 1CompletedPrimary

Phase I Safety and Immunogenicity Study of VAX102 [Flagellin.HuM2e] Influenza Vaccine in Healthy Adults

NCT01049490Not ApplicableCompletedPrimary

Dose Sparing Intradermal S-OIV H1N1 Influenza Vaccination Device

NCT01008020Not ApplicableCompletedPrimary

Effects of Tea Catechin Consumption on the Prophylaxis of Influenza Infection

NCT01225770Phase 3UnknownPrimary

Gargling With Green Tea for Prophylaxis of Influenza Infection in Teenagers

NCT01201902Phase 3CompletedPrimary

A Study to Evaluate the Safety and Immunogenicity of an Inactivated Split-virion Influenza A(H1N1) Vaccine

NCT00812448Not ApplicableCompletedPrimary

Catechin Containing Mask for the Prevention of Influenza Infection

NCT00559975Phase 1CompletedPrimary

Safety, Tolerability, Immunogenicity And CPG Dosage Finding Study of Novartis CpG Adjuvanted Flu Vaccine

NCT00647465Phase 3TerminatedPrimary

Effect of the Interferon Alpha Citizen by Sub-Lingual Way on the Humoral Immunizing Answer

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