Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 80/100

Failure Rate

42.9%

9 terminated/withdrawn out of 21 trials

Success Rate

57.1%

-29.4% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

108%

13 of 12 completed trials have results

Key Signals

13 with results8 terminated

Enrollment Performance

Analytics

Phase 1
18(85.7%)
Phase 2
3(14.3%)
21Total
Phase 1(18)
Phase 2(3)

Activity Timeline

Global Presence

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Clinical Trials (21)

Showing 20 of 21 trials
NCT02401815Phase 1Completed

CGT9486 (Formerly Known as PLX9486) as a Single Agent and in Combination With PLX3397 (Pexidartinib) or Sunitinib in Participants With Advanced Solid Tumors

Role: collaborator

NCT04910152Phase 1Terminated

Novel BET Inhibitor PLX51107 for Steroid-Refractory Acute GVHD

Role: collaborator

NCT01004861Phase 1Completed

Safety Study of PLX108-01 in Patients With Solid Tumors

Role: collaborator

NCT02777710Phase 1Completed

Evaluation of Safety and Activity of an Anti-PDL1 Antibody (DURVALUMAB) Combined With CSF-1R TKI (PEXIDARTINIB) in Patients With Metastatic/Advanced Pancreatic or Colorectal Cancers

Role: collaborator

NCT03158103Phase 1Completed

A Study of MEK162 (Binimetinib) in Combination With Pexidartinib in Patients With Advanced Gastrointestinal Stromal Tumor (GIST)

Role: collaborator

NCT01596751Phase 1Completed

Phase Ib/II Study of PLX 3397 and Eribulin in Patients With Metastatic Breast Cancer

Role: collaborator

NCT01525602Phase 1Completed

Safety Study of PLX3397 and Paclitaxel in Patients With Advanced Solid Tumors

Role: collaborator

NCT01790503Phase 1Completed

A Phase 1b/2 Study of PLX3397 + Radiation Therapy + Temozolomide in Patients With Newly Diagnosed Glioblastoma

Role: collaborator

NCT01217229Phase 2Completed

Safety and Efficacy Study of PLX3397 in Adults With Relapsed or Refractory Hodgkin Lymphoma

Role: collaborator

NCT01826448Phase 1Terminated

A Phase 1b Open Label, Dose Escalation Study of PLX3397 in Combination With Vemurafenib in V600-mutated BRAF Melanoma

Role: collaborator

NCT02452424Phase 1Terminated

A Combination Clinical Study of PLX3397 and Pembrolizumab To Treat Advanced Melanoma and Other Solid Tumors

Role: collaborator

NCT01499043Phase 2Terminated

Pilot Study of PLX3397 in Patients With Advanced Castration-Resistant Prostate Cancer (CRPC)

Role: collaborator

NCT01349036Phase 2Terminated

A Phase 2 Study of PLX3397 in Patients With Recurrent Glioblastoma

Role: collaborator

NCT01349049Phase 1Completed

Phase 1/2 Safety and Efficacy of PLX3397 in Adults With Relapsed or Refractory Acute Myeloid Leukemia (AML)

Role: collaborator

NCT02683395Phase 1Terminated

A Study of PLX51107 in Advanced Malignancies

Role: lead

NCT01804530Phase 1Terminated

Phase 1 Study of PLX7486 as Single Agent in Patients With Advanced Solid Tumors

Role: lead

NCT02673736Phase 1Terminated

A Study of PLX73086 in Advanced Solid Tumors and Locally Advanced or Refractory Tenosynovial Giant Cell Tumor

Role: lead

NCT00405587Phase 1Completed

Safety Study of PLX4032 in Patients With Solid Tumors

Role: lead

NCT01282684Phase 1Completed

Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of PLX5622 in Healthy Adult Volunteers

Role: lead

NCT01090570Phase 1Withdrawn

Safety, Pharmacokinetic (PK), Pharmcodynamic (PD), and Drug-Drug Interaction of PLX3397 in Patients With Rheumatoid Arthritis Who Are Receiving Methotrexate

Role: lead