The purpose of this study is to determine the safety and effectiveness of Azixa in patients with recurrent glioblastoma multiforme
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
56
3.3 mg/m2 of Azixa administered by intravenous infusion over 2 hours once weekly for 3 consecutive weeks every 4 weeks (1 cycle = 4 weeks)
Barrow Neurological Institute
Phoenix, Arizona, United States
Cedars-Sinai Medical Center
Los Angeles, California, United States
Stanford University
Stanford, California, United States
To determine the progression-free survival (PFS) rate
Time frame: Six 28-day cycles from start of therapy
Overall survival
Time frame: 36 months
Overall response rate
Time frame: 18 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Northwestern University
Chicago, Illinois, United States
Tufts Medical Center
Boston, Massachusetts, United States
Lahey Clinic
Burlington, Massachusetts, United States
University of Massachusettes
Worcester, Massachusetts, United States
Darthmouth -Hitchcock Medical Center
Lebanon, New Hampshire, United States
Columbia University
New York, New York, United States
SCCA/University of Washington
Seattle, Washington, United States