Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

0.0%

0 terminated out of 16 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

25%

4 trials in Phase 3/4

Results Transparency

20%

1 of 5 completed with results

Key Signals

1 with results100% success

Data Visualizations

Phase Distribution

6Total
Not Applicable (1)
P 1 (1)
P 3 (4)

Trial Status

Recruiting7
Completed5
Not Yet Recruiting2
Active Not Recruiting1
Unknown1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 5 completed trials

Clinical Trials (17)

Showing 17 of 17 trials
NCT07575308Phase 2Not Yet RecruitingPrimary

HMBeacon: A Phase 2 Study to Evaluate ALN-6400 in Adult and Adolescent Female Patients With VWD and HMB

NCT07560007Active Not Recruiting

The Bleeding Assessment Tool (BAT)

NCT06610201RecruitingPrimary

A Study of Bleeding and Treatment in Participants With Von Willebrand Disease

NCT06433778CompletedPrimary

A Study on the Outcomes of Recombinant Von Willebrand Factor on Demand Treatment and Prevention and Treatment of Bleeding During and After Surgery in Adults With Inherited Von Willebrand Disease in the United Kingdom (UK)

NCT07404644RecruitingPrimary

An Observational Study of Vonicog Alfa (rVWF) in Pediatric Participants With Von Willebrand Disease (vWD)

NCT07410130Not Yet RecruitingPrimary

Clinical Spectrum and Management of Von Willebrand Disease Among Children in Assiut Governorate

NCT07358013RecruitingPrimary

Endothelial Colony-Forming Cells in Patients With VWD, AVWS and Healthy Subjects

NCT07129343Phase 3RecruitingPrimary

A Study of Recombinant Von Willebrand Factor (rVWF) in Chinese Participants With Von Willebrand Disease (vWD)

NCT06754852Phase 1RecruitingPrimary

A Study Assessing HMB-002 in Participants With Von Willebrand Disease

NCT07115004Phase 3RecruitingPrimary

Study to Evaluate Subcutaneous (SC) VGA039 in Patients With Von Willebrand Disease (VWD)

NCT05582993Phase 3RecruitingPrimary

A Study of Vonicog Alfa (rVWF) in Children With Severe Von Willebrand Disease (vWD)

NCT06173024UnknownPrimary

Post Trial Access Program of TAK-577 for Von Willebrand Disease (VWD)

NCT03879135Phase 3CompletedPrimary

A Study of Recombinant Von Willebrand Factor (rVWF) in Pediatric and Adult Participants With Severe Von Willebrand Disease (VWD)

NCT06710262Completed

T-TAS® wS Method Comparison

NCT06651255Not ApplicableNot Yet RecruitingPrimary

Algorithm-based Management to Reduce the Recurrence of GI Bleeding and Severe Epistaxis in Von Willebrand Disease

NCT05695560CompletedPrimary

A Survey to Describe the Experience and Unmet Needs of Persons Living With Von Willebrand Disease (VWD) and Their Caregivers

NCT05265078CompletedPrimary

A Study on Estimated Risks of Certain Adverse Events in Adults With Von Willebrand Disease (VWD) Treated With Veyvondi

Showing all 17 trials

Research Network

Activity Timeline