Key Insights

Highlights

Success Rate

99% trial completion (above average)

Published Results

27 trials with published results (31%)

Research Maturity

84 completed trials (97% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

1.1%

1 terminated out of 87 trials

Success Rate

98.8%

+12.3% vs benchmark

Late-Stage Pipeline

28%

24 trials in Phase 3/4

Results Transparency

32%

27 of 84 completed with results

Key Signals

27 with results99% success

Data Visualizations

Phase Distribution

60Total
P 1 (31)
P 2 (5)
P 3 (20)
P 4 (4)

Trial Status

Completed84
Withdrawn1
Recruiting1
Terminated1

Trial Success Rate

98.8%

Benchmark: 86.5%

Based on 84 completed trials

Clinical Trials (87)

Showing 20 of 20 trials
NCT06574984RecruitingPrimary

Study for Turoctocog Alfa Treatment Regimen in Iraqi Haemophilia A Patients

NCT02141074Phase 3CompletedPrimary

Safety and Efficacy of Nonacog Beta Pegol (N9-GP) in Previously Untreated Patients With Haemophilia B

NCT01467427Phase 3CompletedPrimary

Safety, Efficacy and Pharmacokinetics of NNC-0156-0000-0009 in Previously Treated Children With Haemophilia B.

NCT02137850Phase 3CompletedPrimary

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

NCT02670213CompletedPrimary

A Study of Safety and Effectiveness of NovoThirteen® (rFXIII) During Treatment of Congenital FXIII Deficiency in Japan

NCT01830712CompletedPrimary

A Long-term Assessment of Physical Activity, Range of Motion, and Functional Status Following Elective Orthopedic Surgery in Hemophilia Patients With Inhibitors

NCT01561391Phase 4CompletedPrimary

Safety and Efficacy of Activated Recombinant Human Factor VII in Haemophilia Patients With Inhibitors During and After Major Surgery

NCT03075670Phase 1CompletedPrimary

A Trial Comparing Nonacog Beta Pegol (N9-GP) and ALPROLIX® in Patients With Haemophilia B

NCT03528551Phase 3CompletedPrimary

A Research Study Looking at How a Factor VIII Medicine Called Turoctocog Alfa Pegol (N8-GP) Works in People With Haemophilia A

NCT02207218CompletedPrimary

To Investigate Safety and Efficacy of NovoEight® (rFVIII) During Long-term Treatment of Haemophilia A in Japan

NCT03179748CompletedPrimary

Study Investigating Novoeight®/NovoEight® (Turoctocog Alfa) in Mexican Haemophilia A Patients

NCT03196284Phase 2CompletedPrimary

A Trial Evaluating the Efficacy and Safety of Prophylactic Administration of Concizumab in Haemophilia A and B Patients With Inhibitors

NCT01493778Phase 3CompletedPrimary

Safety and Efficacy of Turoctocog Alfa in Prevention and Treatment of Bleeds in Previously Untreated Children With Haemophilia A

NCT01731600Phase 3CompletedPrimary

A Multinational, Open-Label, Non-Controlled Trial on Safety, Efficacy and Pharmacokinetics of NNC 0129-0000-1003 in Previously Treated Paediatric Patients With Severe Haemophilia A

NCT01480180Phase 3CompletedPrimary

Evaluation of Safety and Efficacy, Including Pharmacokinetics, of NNC 0129-0000-1003 When Administered for Treatment and Prophylaxis of Bleeding in Subjects With Haemophilia A

NCT01489111Phase 3CompletedPrimary

Evaluating the Haemostatic Effect of NNC 0129-0000-1003 During Surgical Procedures in Subjects With Haemophilia A.

NCT02938585Phase 3CompletedPrimary

Efficacy and Safety of Turoctocog Alfa for Prophylaxis and Treatment of Bleeding Episodes in Previously Treated Chinese Patients With Haemophilia A

NCT02035384CompletedPrimary

Safety and Efficacy of Turoctocog Alfa During Long-Term Treatment of Severe and Moderately Severe Haemophilia A

NCT03449342Phase 4CompletedPrimary

Research Study to Look at Side Effects During Regular Injection With Factor VIII Medicine Named Turoctocog Alfa for a 8 Weeks Period

NCT02994407Phase 1CompletedPrimary

Safety, Tolerability, and Pharmacokinetics Study of Turoctocog Alfa Pegol Injected Under the Skin in Patients With Haemophilia A

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