A Phase I, Multicenter, Open-Label, Dose-Escalation Study Evaluating the Safety and Tolerability of Intravenous EZN-2208 (PEG-SN38) Administered Every 3 Weeks in Patients With Advanced Solid Tumors or Lymphoma (EZN-2208-01)
Interventional
Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label
Determine the MTD of i.v. EZN-2208 administered q3wk and recommended Phase 2 dose of i.v. EZN-2208
Razelle Kurzrock, MD
Principal Investigator
M.D. Anderson Cancer Center
United States: Food and Drug Administration
EZN-2208-01
NCT00520637
May 2007
Name | Location |
---|---|
MD Anderson Cancer Center | Houston, Texas 77030-4096 |
Northwestern University, Feinberg School of Medicine, Division of Hematology/Oncology | Chicago, Illinois 60611 |