Key Insights

Highlights

Success Rate

96% trial completion (above average)

Published Results

18 trials with published results (22%)

Research Maturity

66 completed trials (80% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

3.6%

3 terminated out of 83 trials

Success Rate

95.7%

+9.1% vs benchmark

Late-Stage Pipeline

28%

23 trials in Phase 3/4

Results Transparency

27%

18 of 66 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

Completed66
Recruiting8
Enrolling By Invitation3
Terminated3
Unknown1
Not Yet Recruiting1

Trial Success Rate

95.7%

Benchmark: 86.6%

Based on 66 completed trials

Clinical Trials (83)

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

NCT07723560RecruitingPrimary

Study of Surgical Practices in Hemophilia A Patients Treated With Efanesoctocog Alfa (Altuvoct®)

NCT05685238Phase 3RecruitingPrimary

A Research Study Looking at Long-term Treatment With Mim8 in People With Haemophilia A

NCT07653139Not Yet RecruitingPrimary

Patient Preferences in Treatment of Haemophilia A With and Without Inhibitors: a Discrete Choice Experiment in Germany

NCT06574984Completed

Study for Turoctocog Alfa Treatment Regimen in Iraqi Haemophilia A Patients

NCT07238816Phase 1CompletedPrimary

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

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®

NCT03695978RecruitingPrimary

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

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

NCT07437404Phase 3RecruitingPrimary

Efficacy and Safety Evaluation Study of SCT800 in Previously Untreated Hemophilia 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)

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

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

NCT05621746RecruitingPrimary

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

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