The objective of this study is to assess the efficacy and safety of TLN-4601 used to treat patients with Glioblastoma Multiforme(GBM) that recur/progress after receiving first line systemic therapy post surgery/radiotherapy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
14 day continuous IV administration of TLN-4601 at 480 mg/m2/day followed by a 7-day recovery period
Sloan-Kettering Institute for Cancer Research
New York, New York, United States
Duke University
Durham, North Carolina, United States
Ottawa Health Research Institute
Ottawa, Ontario, Canada
The Pencer Brain Tumor Center, Princess Margaret Hospital
Toronto, Ontario, Canada
To assess the efficacy of TLN-4601 in patients with recurrent glioblastoma multiforme (GBM) as measured by 6-month progression free survival from date of initial infusion of TLN-4601 (Day 1, Cycle 1).
Time frame: 6-month progression free survival from date of initial infusion of TLN-4601 (Day 1, Cycle 1)
To examine the safety and tolerability of TLN-4601 in patients with recurrent GBM
Time frame: Maximum 13 months from date of initial infusion of TLN-4601 (Day 1, Cycle 1)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Hôpital Notre-Dame du CHUM
Montreal, Quebec, Canada
Royal Victoria Hospital
Montreal, Quebec, Canada
L'Hotel-Dieu de Quebec
Québec, Quebec, Canada
Centre Hospitalier Universitaire de Sherbrooke
Sherbrooke, Quebec, Canada