Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 80/100

Failure Rate

42.2%

27 terminated/withdrawn out of 64 trials

Success Rate

55.0%

-31.5% vs industry average

Late-Stage Pipeline

22%

14 trials in Phase 3/4

Results Transparency

55%

18 of 33 completed trials have results

Key Signals

1 recruiting18 with results19 terminated8 withdrawn

Enrollment Performance

Analytics

Phase 1
28(43.8%)
Phase 2
22(34.4%)
Phase 3
14(21.9%)
64Total
Phase 1(28)
Phase 2(22)
Phase 3(14)

Activity Timeline

Global Presence

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Clinical Trials (64)

Showing 20 of 64 trials
NCT02891603Phase 1Completed

A Phase I/II GVHD Prevention Trial Combining Pacritinib With Sirolimus-Based Immune Suppression

Role: collaborator

NCT07387354Phase 1Not Yet Recruiting

Pacritinib With Aza for Upfront Myelodysplastic Syndrome

Role: collaborator

NCT04858256Phase 2Recruiting

Pacritinib in Relapsed/Refractory T-cell Lymphoproliferative Neoplasms

Role: collaborator

NCT05552183Phase 1Completed

Study to Evaluate the Safety, Tolerability, and PK of Pacritinib

Role: lead

NCT05657613Phase 1Completed

Drug-Drug Interaction Study of Pacritinib and CYP450,Transporter Substrates, and CYP450 3A4 in Healthy Male Subjects

Role: lead

NCT04404361Phase 2Terminated

PRE-VENT Study in Hospitalized Patients With Severe COVID-19 With or Without Cancer

Role: lead

NCT00268853Phase 2Completed

A Trial in Patients With Diffuse Large-B-cell Lymphoma Comparing Pixantrone Against Doxorubicin

Role: lead

NCT01632436Phase 1Withdrawn

Pharmacokinetic and Safety Study of Pixantrone in Patients With Metastatic Cancer and Hepatic Impairment

Role: lead

NCT01638442Phase 1Completed

Crossover Trial of the Effect of a High-Fat Meal on the PK of Oral CHR 2797 in Healthy Male Subjects

Role: lead

NCT00106600Phase 1Completed

Pixantrone (BBR 2778) in Patients With Refractory Acute Myelogenous Leukemia (AML)

Role: lead

NCT02807207Phase 1Completed

To Evaluate the Cardiac Safety and PK Following a Single Oral Dose Administration of Pacritinib in Healthy Subjects

Role: lead

NCT02823171Phase 1Completed

To Assess the Bioequivalence of Two Pacritinib Drug Product Formulations and FMI Formulation Following Oral Administration in Healthy Subjects

Role: lead

NCT02807116Phase 1Completed

Drug-Interaction Study to Evaluate the Effect of Rifampin, a Potent CYP3A4 Inducer, on the Systemic Exposure of Pacritinib in Healthy Subjects

Role: lead

NCT02808455Phase 1Completed

Study to Assess the Relative Bioavailability of Pacritinib Following Oral Administration as Capsule and Solution Formulations in Healthy Subjects

Role: lead

NCT00493467Phase 2Completed

Zevalin (Ibritumomab Tiuxetan) for Early Stage Indolent Lymphomas

Role: collaborator

NCT03645824Phase 2Active Not Recruiting

Myelofibrosis Treated With Pacritinib Before aSCT. (HOVON134MF)

Role: collaborator

NCT04884191Phase 2Completed

Phase 2 Study: An Open-Label, Randomized, Phase 2 Dose-Finding Study of Pacritinib in Patients With Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, or Post- Essential Thrombocythemia Myelofibrosis Previously Treated With Ruxolitinib

Role: lead

NCT00384111Phase 3Terminated

Phase 3 Study of Zevalin Following R-CVP in Previously Untreated Patients With Follicular Non Hodgkin's Lymphoma (NHL)

Role: collaborator

NCT01321541Phase 3Completed

Comparison of Pixantrone + Rituximab With Gemcitabine + Rituximab in Patients With Aggressive B-cell Non-Hodgkin Lymphoma or Follicular Grade 3 Lymphoma Who Have Relapsed After Therapy and Are Not Eligible for Stem Cell Transplant

Role: lead

NCT02055781Phase 3Terminated

Pacritinib Versus Best Available Therapy to Treat Patients With Myelofibrosis and Thrombocytopenia

Role: lead