Key Insights

Highlights

Success Rate

75% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 52/100

Termination Rate

8.3%

1 terminated out of 12 trials

Success Rate

75.0%

-11.5% vs benchmark

Late-Stage Pipeline

25%

3 trials in Phase 3/4

Results Transparency

33%

1 of 3 completed with results

Key Signals

1 with results75% success

Data Visualizations

Phase Distribution

6Total
P 2 (3)
P 3 (3)

Trial Status

Completed3
Recruiting3
Not Yet Recruiting2
Active Not Recruiting1
Terminated1
Unknown1

Trial Success Rate

75.0%

Benchmark: 86.5%

Based on 3 completed trials

Clinical Trials (12)

Showing 12 of 12 trials
NCT06945861RecruitingPrimary

Immunological Aspect of Thrombotic Thrombocytopenic Purpura (TTP)

NCT05714969Phase 2CompletedPrimary

A Study of TAK-755 (rADAMTS13) With Little to No Plasma Exchange (PEX) Treatment in Adults With Immune-mediated Thrombotic Thrombocytopenic Purpura (iTTP)

NCT04683003Phase 3Active Not RecruitingPrimary

A Study of TAK-755 in Participants With Congenital Thrombotic Thrombocytopenic Purpura

NCT07429942Not Yet RecruitingPrimary

A Study to Learn More About the Treatment of People With Congenital Thrombotic Thrombocytopenic Purpura (cTTP) Who Received Recombinant ADAMTS13 (rADAMTS13) as Part of the Early Access Program

NCT07353099Not Yet RecruitingPrimary

A Study in Children and, Adults With Congenital Thrombotic Thrombocytopenic Purpura (cTTP) Treated With Adzynma

NCT03393975Phase 3CompletedPrimary

A Study of BAX 930 in Children, Teenagers, and Adults Born With Thrombotic Thrombocytopenic Purpura (TTP)

NCT06441578RecruitingPrimary

A Survey of Recombinant ADAMTS13 in Participants With Congenital Thrombotic Thrombocytopenic Purpura

NCT07205861RecruitingPrimary

Retrospective Epidemiological Study of Patients in the National Cohort of the French TMA Center

NCT05770219UnknownPrimary

Expanded Access Program of TAK-755 for Congenital Thrombotic Thrombocytopenic Purpura (cTTP)

NCT00937131Phase 2CompletedPrimary

The Use of Rituximab in Acute Thrombotic Thrombocytopenic Purpura (TTP)

NCT05393999Phase 2Withdrawn

SABRE: A Single-arm Prospective Study Measuring Safety and Tolerability of SARS-CoV-2 Neutralising Antibodies in High-risk Populations

NCT00411801Phase 3TerminatedPrimary

Safety and Efficacy Study to Compare Uniplas With Cryosupernatant Plasma in Thrombotic Thrombocytopenic Purpura (TTP)

Showing all 12 trials

Research Network

Activity Timeline