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Kinase Inhibitor

PLX73086 for Pigmented Villonodular Synovitis

Phase 1
Waitlist Available
Research Sponsored by Plexxikon
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group

Summary

The purpose of this research study is to evaluate safety, pharmacokinetics and preliminary efficacy of the investigational drug PLX73086 in subjects with solid tumors including subjects with locally advanced or refractory tenosynovial giant cell tumor (TGCT).

Eligible Conditions
  • Pigmented Villonodular Synovitis
  • Solid Tumors
  • Giant Cell Tumor

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: PLX73086Experimental Treatment1 Intervention
Part 1: Open-label, sequential PLX73086 dose escalation in approximately 36 solid tumors subjects. Part 2: Extension cohort at the recommended phase 2 dose (RP2D) of PLX73086 in approximately 30 subjects with histologically confirmed, unresectable, locally advanced or refractory TGCT (including metastatic disease).

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Who is running the clinical trial?

PlexxikonLead Sponsor
24 Previous Clinical Trials
1,090 Total Patients Enrolled
~1 spots leftby Oct 2025
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