This study assesses the safety and efficacy of imatinib mesylate treatment of patients with malignant peripheral nerve sheath tumors
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
11
Novartis Investigative Site
Berlin, Germany
Novartis Investigative Site
Hamburg, Germany
Response rate assessed by a Tumor MRI scan every 6 weeks or if clinically indicated.
Time frame: Every 36 weeks
Time to progression assessed by an MRI scan.
Time frame: Every 36 weeks
Overall survival
Time frame: Every 36 weeks
Safety and tolerability assessed by abnormal lab values (hematology, biochemistry, urinalysis), by physical examination and vital signs
Time frame: Every 36 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.