Key Insights

Highlights

Success Rate

86% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 52/100

Termination Rate

10.5%

4 terminated out of 38 trials

Success Rate

86.2%

-0.3% vs benchmark

Late-Stage Pipeline

37%

14 trials in Phase 3/4

Results Transparency

32%

8 of 25 completed with results

Key Signals

8 with results86% success

Data Visualizations

Phase Distribution

23Total
Not Applicable (2)
P 1 (1)
P 2 (6)
P 3 (10)
P 4 (4)

Trial Status

Completed25
Terminated4
Withdrawn3
Unknown3
Recruiting2
Active Not Recruiting1

Trial Success Rate

86.2%

Benchmark: 86.5%

Based on 25 completed trials

Clinical Trials (38)

Showing 20 of 20 trials
NCT04953884Phase 3CompletedPrimary

Efficacy, PK, Immunogenicity and Safety of Wilate in Severe Von Willebrand Disease (VWD) Patients <6 Years of Age

NCT02932618Phase 3RecruitingPrimary

A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD)

NCT02869074CompletedPrimary

Molecular and Clinical Profile of Von Willebrand Disease in Spain

NCT02472665Phase 4RecruitingPrimary

Efficacy and Safety of Fanhdi®, a High-purity Von Willebrand Containing FVIII Concentrate, in Pediatric Patients With Von Willebrand Disease

NCT04657887CompletedPrimary

Registry of Patients With Von WilLEbrand Disease Treated With Voncento®

NCT00555555Phase 4Active Not RecruitingPrimary

Efficacy of Alphanate FVIII/VWF Concentrate in Type 3 Von Willebrand Patients

NCT02792205CompletedPrimary

Performance Evaluation of Von Willebrand:Collagen-Binding Assays to Diagnose Von Willebrand Factor Deficiency in Patients With Increased Risk of Bleeding

NCT02973087Phase 3CompletedPrimary

rVWF IN PROPHYLAXIS

NCT02283268Phase 3CompletedPrimary

Recombinant Von Willebrand Factor in Subjects With Severe Von Willebrand Disease Undergoing Surgery

NCT01410227Phase 3CompletedPrimary

Pharmacokinetics, Safety and Efficacy of Recombinant Von Willebrand Factor (rVWF) in the Treatment of Bleeding Episodes in Von Willebrand Disease (VWD)

NCT00816660Phase 1CompletedPrimary

Pharmacokinetic, Safety and Tolerability Study of Recombinant Von Willebrand Factor / Recombinant Factor VIII Complex in Type 3 Von Willebrand Disease

NCT01602419CompletedPrimary

Surveillance of Safety and Efficacy of Wilate in Patients With Von Willebrand Disease

NCT03521583UnknownPrimary

Von Willebrand Disease in the Netherlands

NCT04279717UnknownPrimary

Latin-American Von Willebrand Disease Registry

NCT00524225Phase 2TerminatedPrimary

IL-11 in Adults With Von Willebrand Disease Undergoing Surgery

NCT01949220CompletedPrimary

Willebrand International Non-interventional Global Surveillance

NCT02552576Phase 4CompletedPrimary

Study of Voncento® in Subjects With Von Willebrand Disease

NCT02246881Phase 3CompletedPrimary

A Study to Compare the Pharmacokinetics and Safety of Current Factor VIII Concentrate and Optivate® in Haemophilia A.

NCT00524342Phase 2CompletedPrimary

IL-11 in Women With Von Willebrand Disease and Refractory Menorrhagia

NCT01651468Not ApplicableWithdrawnPrimary

The Effect of the Nutraceutical "Hemofix" on the Coagulation System

Scroll to load more

Research Network

Activity Timeline