Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

14.3%

4 terminated/withdrawn out of 28 trials

Success Rate

83.3%

-3.2% vs industry average

Late-Stage Pipeline

43%

12 trials in Phase 3/4

Results Transparency

35%

7 of 20 completed trials have results

Key Signals

1 recruiting7 with results

Enrollment Performance

Analytics

Phase 3
10(47.6%)
N/A
4(19.0%)
Phase 2
3(14.3%)
Phase 4
2(9.5%)
Phase 1
2(9.5%)
21Total
Phase 3(10)
N/A(4)
Phase 2(3)
Phase 4(2)
+1 more

Activity Timeline

Global Presence

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Clinical Trials (28)

Showing 20 of 28 trials
NCT02972281Not ApplicableCompleted

Systematic Search for Primary Immunodeficiency in Adults With Infections

Role: collaborator

NCT06257407Recruiting

Perioperative Hemostasis Management in Liver Transplantation

Role: collaborator

NCT02352181Not ApplicableCompleted

Management of Coagulopathy During Orthotopic Liver Transplantation. Comparison Between ROTEM-based Management and Standard Biological Assessment.

Role: collaborator

NCT05695391Phase 3Terminated

A Phase 3 Study of the Safety and Efficacy of Coagulation Factor VIIa (Recombinant) for the Prevention of Excessive Bleeding in Patients With Congenital Hemophilia A or B With Inhibitors to Factor VIII or IX Undergoing Elective Major Surgical Procedures SCOPE HIM

Role: lead

NCT05904210Completed

Retrospective Experience Assessing the Real-World Utilization and Effectiveness of SEVENFACT®

Role: lead

NCT01676688Completed

Safety Study of Alfalastin (Human Alpha-1 Antitrypsin) Administered at Home

Role: lead

NCT05664035Not Yet Recruiting

SPAD in Adult Patients

Role: collaborator

NCT02448680Phase 3Completed

A Phase III Study on the Safety, Pharmacokinetics and Efficacy of Coagulation Factor VIIa

Role: lead

NCT02548143Phase 3Completed

LR769 in Congenital Hemophilia Patients With Inhibitors Undergoing Elective Surgery or Invasive Procedures

Role: lead

NCT04350580Phase 3Completed

Polyvalent Immunoglobulin in COVID-19 Related ARds

Role: collaborator

NCT02317562Phase 3Terminated

Efficacy and Safety Study of I10E in the Maintenance Treatment of Patients With CIDP: Extension of PRISM Study I10E-1302

Role: lead

NCT02293460Phase 3Completed

Efficacy and Safety Study of I10E in Treatment of Patients With CIDP

Role: lead

NCT02155725Phase 4Completed

Fibrinogen in Haemorrhage of Delivery

Role: lead

NCT03370627Not ApplicableCompleted

Effect of Anti-CD303 Antibodies in Autoimmune Diseases

Role: collaborator

NCT02287896Phase 2Completed

Pharmacokinetics and Safety of Roledumab in RhD-negative Pregnant Women Carrying an RhD-positive Foetus

Role: lead

NCT02488525Phase 3Terminated

Prevention of Hemorrhage After Implantation of Mechanical Circulatory Support

Role: collaborator

NCT01949220Completed

Willebrand International Non-interventional Global Surveillance

Role: lead

NCT02020369Phase 3Completed

Phase III Study of Coagulation FVIIa (Recombinant) in Congenital Hemophilia A or B Patients With Inhibitors

Role: collaborator

NCT01951924Phase 3Completed

LIME Study (LFB IVIg MMN Efficacy Study)

Role: lead

NCT02094430Phase 2Completed

Human Fibrinogen Concentrate (FGTW) in Pediatric Patients With Congenital Fibrinogen Deficiency

Role: lead