The purpose of this study is to evaluate the safety, tolerance, pharmacokinetics, and biological effects of escalating single and multiple doses of recombinant human tumor necrosis factor (rHuTNF) administered by intravenous infusion to patients with histologically documented advanced malignancies that are resistant or non-amenable to conventional therapy.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000096-29S1
Application #
3884850
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
29
Fiscal Year
1990
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
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