Expanded Access Protocol for PV-10 for Cutaneous or Subcutaneous Tumors

Exclusion Criteria

• •1. Cancer patients who are eligible for an existing PV-10 clinical trial.
• •2. Certain photosensitizing agents within 5 half-lives prior to PV-10 administration.
• •3. Concurrent or Intercurrent Illness:
• •* Subjects with uncontrolled diabetes or extremity complications due to diabetes.
• •* Subjects with severe peripheral vascular disease.
• •* Subjects with significant concurrent or intercurrent illness, psychiatric disorders, or alcohol or chemical dependence that would, in the opinion of the Investigator, compromise their safety or compliance or interfere with interpretation of study results.
• •* Subjects with uncontrolled thyroid disease, goiter, partial thyroidectomy, radioiodine- or surgically-treated Graves' hyperthyroidism or cystic fibrosis.
• •* Subjects with clinically significant acute or unstable cardiovascular, (stroke), renal, gastrointestinal, pulmonary, immunological (with the exception of the presence of hepatitis B virus (HBV), viral hepatitis, or cirrhosis), endocrine, or central nervous system disorders.
• •4. Pregnancy:
• •* Female subjects who are pregnant or lactating.
• •* Female subjects who have positive serum ßHCG pregnancy test taken within 7 days of PV-10 administration.
• •* Fertile subjects who are not using effective contraception.
• •5. Investigational Agents:
• •* Subjects who have received investigational agents within 4 weeks (or 5 half-lives) of study administration.