Key Insights

Highlights

Success Rate

96% trial completion (above average)

Published Results

18 trials with published results (22%)

Research Maturity

64 completed trials (79% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

3.7%

3 terminated out of 81 trials

Success Rate

95.5%

+9.0% vs benchmark

Late-Stage Pipeline

28%

23 trials in Phase 3/4

Results Transparency

28%

18 of 64 completed with results

Key Signals

18 with results96% success

Data Visualizations

Phase Distribution

51Total
Not Applicable (1)
P 1 (24)
P 2 (3)
P 3 (20)
P 4 (3)

Trial Status

Completed64
Recruiting8
Terminated3
Enrolling By Invitation3
Unknown1
Withdrawn1

Trial Success Rate

95.5%

Benchmark: 86.5%

Based on 64 completed trials

Clinical Trials (81)

Showing 20 of 20 trials
NCT07220564Phase 1RecruitingPrimary

A Research Study Looking at How Different Doses of Study Medicine (Inno8) Work in the Body of People With Haemophilia A

NCT02207894RecruitingPrimary

A Survey on the Success of Inhibitor Elimination Using Individualized Concentrate Selection and Controlled ITI

NCT06649630Phase 1CompletedPrimary

A Study Looking at How Different Doses of Study Medicine (Inno8) Works in the Body of Healthy Men

NCT05685238Phase 3Active Not RecruitingPrimary

A Research Study Looking at Long-term Treatment With Mim8 in People With Haemophilia A (FRONTIER 4)

NCT07437404Phase 3RecruitingPrimary

Efficacy and Safety Evaluation Study of SCT800 in Previously Untreated Hemophilia A Patients.

NCT06574984Recruiting

Study for Turoctocog Alfa Treatment Regimen in Iraqi Haemophilia A Patients

NCT05082116Phase 3CompletedPrimary

Efficacy and Safety of Turoctocog Alfa Pegol (N8-GP) for Prophylaxis and Treatment of Bleeding Episodes in Previously Treated Chinese Patients With Haemophilia A (pathfinder10)

NCT07238816Phase 1RecruitingPrimary

A Research Study Looking at How Food Intake Affects Inno8 in the Body of Healthy People

NCT02137850Phase 3Completed

Safety and Efficacy of Turoctocog Alfa Pegol (N8-GP) in Previously Untreated Patients With Haemophilia A

NCT04574076Enrolling By InvitationPrimary

A Study Following Males With Haemophilia A on Prophylaxis With Esperoct®

NCT05878938Phase 3CompletedPrimary

A Research Study Looking at How Safe it is to Switch From Emicizumab to Mim8 in People With Haemophilia A (FRONTIER 5)

NCT05053139Phase 3CompletedPrimary

A Research Study Investigating Mim8 in Adults and Adolescents With Haemophilia A With or Without Inhibitors

NCT03695978RecruitingPrimary

Efficacy, Safety & Utilisation of Nuwiq, Octanate and Wilate in Previously Untreated & Minimally Treated Haemophilia A Patients

NCT05681845Phase 1CompletedPrimary

A Study to Compare the Blood Levels of Mim8 in Healthy Men When Administered With the DV3407-C1 Pen Injector or a Syringe and Cartridge

NCT04682145Enrolling By InvitationPrimary

Adverse Event Data Collection From the EUHASS Registry on Turoctocog Alfa Pegol

NCT06285071Enrolling By InvitationPrimary

Post-Marketing Surveillance (All Case Surveillance) on Treatment With Alhemo® in Patients With Haemophilia A or Haemophilia B With Inhibitors

NCT04334057CompletedPrimary

Post-Marketing Surveillance (Use-results Surveillance) With Esperoct®

NCT05621746RecruitingPrimary

An Observational Research Study of the Health of Joints in People With Haemophilia Taking the Medicine Esperoct

NCT04675541CompletedPrimary

Register of Patients With haEmophilia A tReated With Afstyla®

NCT03055611CompletedPrimary

A Study to Evaluate the Real-world Usage and Effectiveness of Elocta and Alprolix in Patients With Haemophilia A or B

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