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4 terminated/withdrawn out of 28 trials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

85.2%

-1.3% vs industry average

Late-Stage Pipeline

82%

23 trials in Phase 3/4

Results Transparency

43%

10 of 23 completed trials have results

Key Signals

10 with results

Enrollment Performance

Analytics

Phase 3
19(70.4%)
Phase 4
4(14.8%)
Phase 2
2(7.4%)
Phase 1
2(7.4%)
27Total
Phase 3(19)
Phase 4(4)
Phase 2(2)
Phase 1(2)

Activity Timeline

Global Presence

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Clinical Trials (28)

Showing 20 of 28 trials
NCT03161626Completed

Registry Study of COAGADEX® Patients With Moderate or Severe Hereditary Factor X Deficiency Undergoing Major Surgery

Role: lead

NCT01811875Phase 4Terminated

Post-Marketing Safety Study Following Long-Term Prophylactic OptivateTreatment in Subjects With Severe Haemophilia A

Role: lead

NCT03264157Phase 2Completed

Safety and Effectiveness of BPL HRIG With Active Rabies Vaccine in Healthy Subjects

Role: lead

NCT01086852Phase 3Terminated

Safety & Efficacy of BPL's High Purity FACTOR X in Treatment of Factor X Deficient Subjects Undergoing Surgery

Role: lead

NCT01884311Phase 3Completed

Pharmacokinetics (PK) and Safety of Subgam-VF in Primary Immunodeficiency Diseases

Role: lead

NCT01721681Phase 3Completed

A Study to Investigate Bio Product Laboratory Ltd (BPL's) Factor X in the Prophylaxis of Bleeding in Children <12 Years

Role: lead

NCT02246842Phase 1Completed

A Study Comparing the Pharmacokinetics and Tolerance of D-Gam® to Rhophylac® in Rh-D-negative Healthy Volunteers.

Role: lead

NCT02246855Phase 1Completed

A Comparison of the Pharmacokinetics, Safety and Tolerance of Two Formulations of a Liquid IVIg in Healthy Volunteers

Role: lead

NCT02250560Phase 3Completed

A Study to Investigate the Safety and Efficacy of Replenine®-VF in Haemophilia B Patients Undergoing Major Surgery.

Role: lead

NCT02231944Phase 3Completed

An Open Study to Investigate the Safety and Efficacy of Replenine®-VF in Severe Haemophilia B Patients

Role: lead

NCT02250573Phase 3Completed

An Open-study to Investigate the Safety and Efficacy of Replenine®-VF in Haemophilia B Subjects Undergoing Surgery

Role: lead

NCT02247154Phase 4Completed

A Study of the Safety and Efficacy of Vigam® Liquid in Patients With Primary or Secondary Antibody Deficiency

Role: lead

NCT02246868Phase 3Completed

An Open Study to Investigate the Safety and Efficacy of Optivate® in Severe Haemophilia A Patients.

Role: lead

NCT02246894Phase 3Completed

A Study to Investigate the Safety and Efficacy of Optivate® in Children Under 6 Years of Age With Haemophilia A.

Role: lead

NCT02250508Phase 2Completed

A Study to Compare the Pharmacokinetics and Safety of Optivate® and Haemate P® in Patients With Von Willebrand Disease.

Role: lead

NCT02250482Phase 3Completed

An Open Study to Investigate the Safety and Efficacy of Optivate® in Haemophilia A Patients Undergoing Surgery.

Role: lead

NCT02246881Phase 3Completed

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

Role: lead

NCT02247141Phase 3Completed

A Multi-centre Open Study to Assess the Safety and Efficacy of Subgam®

Role: lead

NCT01963143Phase 3Completed

Bioequivalence Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Gammaplex® 10 and Gammaplex® 5% in Primary Immunodeficiency Diseases

Role: lead

NCT02199925Phase 4Unknown

An Open-Label Study to Evaluate the Efficacy of High-Dose Gammaplex in Children on the Autism Spectrum

Role: collaborator