Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
GenVec
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patient must be 18 years old or older, and able to give informed consent.
You may not be if
Patients must have one or more tumor nodules accessible for direct injection.
Patients with metastases outside the treatment field may be enrolled if the sites of metastases do not limit survival expectancy to less than 3 months.
Patients must be unlikely to derive significant potential benefit from other treatment options and no other treatments should be anticipated during the study treatment period or a period of two months thereafter.
Patient's Karnofsky performance status must be greater than or equal to 70%.
Chemotherapy or experimental medications within the last four weeks prior to Day 1.
Active disease of the central nervous system.
Baseline liver enzymes (AST, ALT, bilirubin, alkaline phosphatase) greater than 3 times the upper limit normal.
Renal insufficiency (Serum creatinine greater than 2.0 mg/dL).
Coagulopathy (PT INR \>1.5 or PTT ratio \>1.5 in patients not receiving anticoagulants).
Significant anemia (e.g. hematocrit \<28% or hemoglobin \<9 g/dL). May have RBC transfusion, or thrombocytopenia (platelet count less than 100,000/μl); or leukopenia (WBC \<3000/μl; ANC \<1500/μl).
Patients with documented history of deep venous thrombosis, pulmonary embolus, cerebrovascular disease, stroke, or TIA.
Patients with history of coagulopathy or known thrombophillic disorders.
Clinical evidence of active infection of any type, including hepatitis B or C virus.
Pregnant or lactating women. It is recommended that both men and women use condoms or another barrier method of birth control for at least 2 months following the last administration of TNFerade™ biologic and some form of birth control for at least 1 year.
Significant concurrent medical or psychiatric illness which, in the opinion of the investigator, would interfere with the patient's ability to participate in the trial
Chronic systemic corticosteroid use, orally or parenterally administered.
Known sensitivity to lidocaine, procaine or amide local anesthetics (used for topical anesthesia).
Surgery within the last 4 weeks prior to day 1 (if patient was ambulatory within 48 hours of surgery, patient may be considered eligible)
Attempted resection of the tumor to be treated, or surgery on the area to be treated, with incomplete healing of surgical wound. (If the surgical wounds are completely healed and lesion continues to progress, patient may be enrolled.)
Patients with a history of clinical lymphedema in the area to be treated.
