RAD001 for Patients With Radioiodine Refractory Thyroid Cancer

Exclusion Criteria

• •Patients receiving anticancer therapies within last 2 weeks or who have received radiation therapy within 3 weeks of study day 1
• •Prior therapy with mTOR inhibitors
• •Patients who have had a major surgery or significant traumatic injury within 4 weeks of start of study drug, patients who have not recovered from the side effects of any major surgery or patients that may require major surgery during the course of the study
• •Prior treatment with any investigational drug within the preceding 3 weeks
• •Patients receiving chronic, systemic treatment with corticosteroids or another immunosuppressive agent. Topical or inhaled corticosteroids are allowed.
• •Patients should not receive immunization with attenuated live vaccines within 2 weeks of study entry or during study period
• •Uncontrolled brain or leptomeningeal metastases, including patients who continue to require glucocorticoids for brain or leptomeningeal metastases
• •Other malignancies within the past 3 years except for adequately treated carcinoma of the cervix or basal or squamous cell carcinomas of the skin
• •Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study
• •A known history of HIV seropositivity
• •Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of RAD001
• •Patients with an active, bleeding diathesis
• •Female patients who are pregnant or breast feeding, or adults of reproductive potential who are not using effective birth control methods
• •Patients who have received prior treatment wih an mTOR inhibitor
• •Patients with a known hypersensitivity to RAD001 or other rapamycins or to its excipients
• •History of noncompliance to medical regimens