A Phase I, Study to Evaluate the Safety and Tolerability of Intravenous EZN-2208 in Patients With Advanced Solid Tumors or Lymphoma (EZN-2208-02)
Completed · Phase 1
Conditions studied: Lymphoma, Advanced Solid Tumors
In brief
The goal of this clinical research study is to find the highest tolerable dose of EZN-2208 that can be given to patients with advanced cancer or lymphoma. The safety of the study drug and its effect on the disease will also be studied. Enzon will also perform pharmacokinetic (PK) testing of EZN-2208. PK testing measures the amount of a drug in the body at different time points.
Key facts
- Study ID
- NCT00520390
- Run by
- Enzon Pharmaceuticals, Inc.
- People needed
- 34
- Starts
- 2007-05-01
- Last updated by the study team
- 2010-04-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologically or cytologically confirmed diagnosis of advanced and/or metastatic solid tumor or lymphoma that is refractory to standard therapy
- Measurable or evaluable disease
- Score of 0 to 2 on the ECOG performance scale
You may not qualify if…
- Concurrent serious medical illness
- Known, clinically suspected, or history of central nervous system (CNS) tumor involvement
- Active diarrhea
- Known history of coagulation disorder
- Patients requiring cytochrome P450 3A4 (CYP3A4) enzyme inducing medications
- Requirement for ketoconazole or other strong inhibitor of CYP3A4 enzymes
- Prior chemotherapy, immunotherapy, investigational agent, or other therapy used to treat the cancer within 4 weeks (6 weeks for prior treatment with mitomycin C or nitrosoureas) prior to the scheduled administration of EZN-2208.
Where it is running
- South Texas Accelerated Research Therapeutics — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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