Key Insights

Highlights

Success Rate

85% trial completion

Published Results

15 trials with published results (47%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

9.4%

3 terminated out of 32 trials

Success Rate

85.0%

-1.5% vs benchmark

Late-Stage Pipeline

59%

19 trials in Phase 3/4

Results Transparency

88%

15 of 17 completed with results

Key Signals

15 with results85% success

Data Visualizations

Phase Distribution

30Total
Not Applicable (4)
P 1 (6)
P 2 (1)
P 3 (15)
P 4 (4)

Trial Status

Completed17
Recruiting4
Terminated3
Active Not Recruiting3
Not Yet Recruiting2
Withdrawn2

Trial Success Rate

85.0%

Benchmark: 86.5%

Based on 17 completed trials

Clinical Trials (32)

Showing 20 of 20 trials
NCT07548411Phase 1Active Not RecruitingPrimary

To Evaluate the Safety and Efficacy of GS1191-0445 Injection in the Treatment of Severe Hemophilia A

NCT05181618Phase 4Active Not RecruitingPrimary

A Study to Evaluate Overall Health, Physical Activity, and Joint Outcomes in Participants With Severe or Moderate Hemophilia A Without Factor VIII Inhibitors on Emicizumab Prophylaxis

NCT04431726Phase 3Active Not RecruitingPrimary

A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Subcutaneous Emicizumab in Participants From Birth to 12 Months of Age With Hemophilia A Without Inhibitors

NCT07446010Not Yet RecruitingPrimary

Post Approval Observational Study to Learn More About How Safe Octocog Alfa is and How Well it Works in Patients With Severe Hemophilia A in India

NCT06703606Phase 1RecruitingPrimary

A Study to Learn About How Changing Therapy From Emicizumab to Marstacimab Affects People With the Severe Hemophilia A.

NCT06938542Not ApplicableEnrolling By Invitation

Palliative Care Needs of Children With Rare Diseases and Their Families

NCT05935358Phase 4RecruitingPrimary

Nuwiq for Perioperative Management Of Patients With Haemophilia A on Emicizumab Regular Prophylaxis Study

NCT04046848Phase 1TerminatedPrimary

Safety and Pharmacokinetics of Subcutaneous Injection of OCTA101 in Adult Patients With Severe Hemophilia A

NCT00323856Phase 4CompletedPrimary

Safety Study of Alphanate in Previously Treated Patients With Severe Hemophilia A

NCT06136507Phase 3Not Yet RecruitingPrimary

Study of Efficacy and Safety of FRSW107 in Pediatric Patients With Severe Hemophilia A

NCT05127681Not ApplicableTerminatedPrimary

Bone Microarchitecture in Men With Hemophilia

NCT06142552Phase 3RecruitingPrimary

Phase 3 Clinical Project of Pegylated Recombinant Human Coagulation Factor VIII-Fc Fusion Protein

NCT06137092Phase 3CompletedPrimary

rFVIII-Fc (Produced by AryoGen Pharmed Co.) Pharmacokinetic Study

NCT04864743Phase 1CompletedPrimary

A Study to Evaluate the Pharmacokinetics,Safety and Tolerability of PEG Recombinant Human Coagulation Factor VIII-Fc Fusion Protein for Injection

NCT05802836RecruitingPrimary

Dynamics of the Anti-factor VIII Antibody Signature During Treatment With Emicizumab

NCT05265286Phase 2CompletedPrimary

A Study of Repeat Dosing of PEG Recombinant Human Coagulation Factor VIII-Fc Fusion Protein for Injection

NCT02172950Phase 3Completed

An Open-label Safety and Efficacy Study of Recombinant FVIII in Patients With Severe Hemophilia A

NCT01051076Not ApplicableCompletedPrimary

Rescue Immunotolerance Study in Induction of Immune Tolerance (ITI)-Experienced Patients (RES.I.S.T. Experienced)

NCT01992549Phase 3CompletedPrimary

Study to Investigate Immunogenicity, Efficacy and Safety of Treatment With Human-cl rhFVIII

NCT01712438Phase 3CompletedPrimary

Human Cell Line-derived Recombinant Factor VIII (Human-cl-rhFVIII) in Previously Untreated Patients

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