Safety Study of PLX108-01 in Patients With Solid Tumors



Status:Active, not recruiting
Conditions:Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:2/27/2019
Start Date:October 2009
End Date:September 2020

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A Phase 1 Study to Assess Safety, Pharmacokinetics, and Pharmacodynamics of PLX3397 in Patients With Advanced, Incurable, Solid Tumors in Which the Target Kinases Are Linked to Disease Pathophysiology

PLX3397 is a selective inhibitor of Fms, Kit, and oncogenic Flt3 activity. The primary
objective of this study is to evaluate the safety and pharmacokinetics of orally administered
PLX3397 in patients with advanced, incurable, solid tumors in which these target kinases are
linked to disease pathophysiology. The secondary objective is to measure the pharmacodynamic
activity of PLX3397 via blood, plasma and urine biomarkers of Fms activity.


Inclusion Criteria:

- Age 18 and older

- Solid tumors refractory to standard therapy

- For the Extension cohorts, patients must have measurable disease by RECIST criteria
and meet the following disease-specific criteria:

- For advanced or recurrent mucoepidermal carcinoma (MEC) of the salivary gland,
patients must not be candidates for curative surgery or radiotherapy.

- For pigmented villo-nodular synovitis (PVNS), patients must have a histologically
confirmed diagnosis of inoperable progressive or relapsing PVNS, or resectable
tumor requesting mutilating surgery, as well as demonstrated progressive disease
in the last 12 months.

- For gastrointestinal stromal tumors (GIST), patients must have failed previous
therapy with imatinib and sunitinib. Patients with known PDGFR mutations are
excluded, but mutation testing is not required for study entry.

- For anaplastic thyroid cancer (ATC), patients must have histologically or
cytologically diagnosed advanced ATC.

- For metastatic solid tumors with documented malignant pleural and/or peritoneal
effusions, patients must not be receiving specific therapy for the effusion or
have an indwelling drain.

- ECOG performance status 0 or 1

- Life expectancy >= 3 months

- Adequate hepatic, renal, and bone marrow function

Exclusion Criteria:

- Specific anti-cancer therapy within 3 weeks of study start

- Uncontrolled intercurrent illness

- Refractory nausea or vomiting, or malabsorption

- Mean QTc >= 450 msec (for males) or QTc >= 470 msec (for females)
We found this trial at
13
sites
185 Cambridge Street
Boston, Massachusetts 02114
617-724-5200
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450 Brookline Ave
Boston, Massachusetts 2215
617-632-3000
Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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Dallas, Texas 75246
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Denver, Colorado 80218
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9280 W. Sunset Road Suite 100
Las Vegas, Nevada 89148
702.952.1251
Comprehensive Cancer Centers of Nevada Comprehensive Cancer Centers of Nevada (CCCN) is the award-winning multidisciplinary...
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Los Angeles, California 90095
(310) 825-4321
UCLA UCLA's primary purpose as a public research university is the creation, dissemination, preservation and...
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Nashville, Tennessee 37232
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5900 Lake Wright Dr
Norfolk, Virginia 23502
(757) 466-8683
Virginia Oncology Associates Virginia Oncology Associates is an oncology and hematology practice of physicians, specializing...
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Philadelphia, Pennsylvania 19106
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Philadelphia, Pennsylvania 19111
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Scottsdale, Arizona 85258
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Spokane, Washington 99218
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Spokane, WA
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