Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 20/100

Failure Rate

9.1%

1 terminated/withdrawn out of 11 trials

Success Rate

66.7%

-19.8% vs industry average

Late-Stage Pipeline

64%

7 trials in Phase 3/4

Results Transparency

100%

2 of 2 completed trials have results

Key Signals

5 recruiting2 with results

Enrollment Performance

Analytics

Phase 3
5(45.5%)
Phase 1
3(27.3%)
Phase 4
2(18.2%)
Phase 2
1(9.1%)
11Total
Phase 3(5)
Phase 1(3)
Phase 4(2)
Phase 2(1)

Activity Timeline

Global Presence

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Clinical Trials (11)

Showing 11 of 11 trials
NCT03165734Phase 3Active Not Recruiting

A Phase 3 Study of Pacritinib in Patients With Primary Myelofibrosis, Post Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis

Role: collaborator

NCT06752850Phase 4Active Not Recruiting

A Study to Investigate the Course of Synovial Hypertrophy in Patients With Haemophilia A on Efanesoctocog Alfa Prophylaxis

Role: collaborator

NCT06782373Phase 2Recruiting

A Study to Assess the Effectiveness and Safety of Pacritinib in Patients With VEXAS Syndrome (PAXIS)

Role: collaborator

NCT06716814Phase 3Recruiting

Study to Provide Continued Access to Treatment for Patients Completing a Previous Trial With Efanesoctocog Alfa

Role: collaborator

NCT05413850Phase 1Recruiting

Anti-tumour Activity of (177Lu) rhPSMA-10.1 Injection

Role: collaborator

NCT06940830Phase 4Recruiting

Long-term Study Evaluating Joint Health in People With Haemophilia A Receiving Real-world Prophylactic Treatment With Efanesoctocog Alfa

Role: collaborator

NCT06579144Phase 1Recruiting

Pharmacokinetic Comparison of Efanesoctocog Alfa vs Other EHL-rFVIII Products in Participants With Severe Haemophilia A

Role: collaborator

NCT03049189Phase 3Active Not Recruiting

Efficacy and Safety of 177Lu-edotreotide PRRT in GEP-NET Patients

Role: collaborator

NCT04907968Phase 1Terminated

Study of Upifitamab Rilsodotin in Combination With Carboplatin in Participants With High-grade Serous Ovarian Cancer

Role: collaborator

NCT02557035Phase 3Completed

An Efficacy and Safety Study of Intravenous Palonosetron Administered as an Infusion and as a Bolus for the Prevention of Nausea and Vomiting

Role: collaborator

NCT02517021Phase 3Completed

A Safety Study of Intravenous Pro-Netupitant and Palonosetron Combination for the Prevention of Nausea and Vomiting

Role: collaborator

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