Success Metrics

Clinical Success Rate
94.1%

Based on 16 completed trials

Completion Rate
94%(16/17)
Active Trials
1(6%)
Results Posted
50%(8 trials)
Terminated
1(6%)

Phase Distribution

Ph phase_1
5
28%
Ph phase_4
1
6%
Ph phase_2
1
6%
Ph phase_3
6
33%

Phase Distribution

5

Early Stage

1

Mid Stage

7

Late Stage

Phase Distribution13 total trials
Phase 1Safety & dosage
5(38.5%)
Phase 2Efficacy & side effects
1(7.7%)
Phase 3Large-scale testing
6(46.2%)
Phase 4Post-market surveillance
1(7.7%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

94.1%

16 of 17 finished

Non-Completion Rate

5.9%

1 ended early

Currently Active

1

trials recruiting

Total Trials

18

all time

Status Distribution
Active(1)
Completed(16)
Terminated(1)

Detailed Status

Completed16
Recruiting1
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
18
Active
1
Success Rate
94.1%
Most Advanced
Phase 4

Trials by Phase

Phase 15 (38.5%)
Phase 21 (7.7%)
Phase 36 (46.2%)
Phase 41 (7.7%)

Trials by Status

recruiting16%
terminated16%
completed1689%

Recent Activity

Clinical Trials (18)

Showing 18 of 18 trials
NCT06574984

Study for Turoctocog Alfa Treatment Regimen in Iraqi Haemophilia A Patients

Recruiting
NCT04584892

Turoctocog Alfa in Haemophilic Italian Patients: Protection and Engagement in Recreational Activities

Completed
NCT03196297Phase 2

A Trial Evaluating Efficacy and Safety of Prophylactic Administration of Concizumab in Patients With Severe Haemophilia A Without Inhibitors

Completed
NCT02207218

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

Completed
NCT03179748

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

Completed
NCT01493778Phase 3

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

Completed
NCT02938585Phase 3

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

Completed
NCT03588741Phase 3

Evaluation of Safety Following Immune Tolerance Induction Treatment With Turoctocog Alfa in Patients With Haemophilia A Following Inhibitor Development in NN7170-4213 Trial

Terminated
NCT02035384

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

Completed
NCT03449342Phase 4

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

Completed
NCT02941354Phase 1

Evaluating the Pharmacokinetics of NovoEight® (Turoctocog Alfa) in Relation to BMI in Subjects With Haemophilia A

Completed
NCT00984126Phase 3

Safety and Efficacy of Turoctocog Alfa (N8) in Prevention and On-demand Treatment of Bleeding Episodes in Subjects With Haemophilia A: An Extension to Trials NN7008-3543, NN7008-3545, NN7008-3600, NN7008-3893 and NN7008-4015

Completed
NCT01138501Phase 3

Safety and Efficacy of Turoctocog Alfa in Previously Treated Male Children With Haemophilia A

Completed
NCT00840086Phase 3

Safety and Efficacy of Turoctocog Alfa in Haemophilia A Subjects

Completed
NCT01692925Phase 1

Investigation of the Pharmacokinetics of Turoctocog Alfa in Subjects With Haemophilia A

Completed
NCT01365520Phase 1

A Single Dose Trial of NNC 0155-0000-0004 in Patients With Haemophilia A

Completed
NCT00837356Phase 1

Comparison of the Action of Drugs in the Body and Safety of N8 and Advate® in Haemophilia A Subjects

Completed
NCT01238367Phase 1

A Single Dose Trial of Recombinant Factor VIII (N8) in Japanese Subjects With Haemophilia A: An Extension to Trial NN7008-3543

Completed

All 18 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
18