Trial of RAD001 and Neurocognition in Tuberous Sclerosis Complex (TSC)

Inclusion criteria

• Male or female patients ages 6 to 21 years of age.
• IQ ≥60.
• Ability to participate in direct neuropsychological and developmental testing.
• English as primary language.
• Diagnosis of tuberous sclerosis complex confirmed by genetic testing and/or clinically definite diagnosis of tuberous sclerosis complex according to the modified Gomez criteria and an IQ>60.
• Stable anti-epileptic drugs (no changes in medications except dose for >6 months).
• Adequate renal function. The GFR would be greater than 50 ml/min.m2 as determined by the Schwartz Formula for children and MDRD for adults:

http://www.nkdep.nih.gov/professionals/gfr\_calculators/index.htm

• If female and of child bearing potential, documentation of negative pregnancy test prior to enrollment. Sexually active pre-menopausal female patients (and female partners of male patients) must use adequate contraceptive measures, excluding estrogen containing contraceptives, while on study. Abstinence will be considered an adequate contraceptive measure.
• INR ≤1.5 (Anticoagulation is allowed if target INR ≤ 1.5 on a stable dose of warfarin or on a stable dose of LMW heparin for >2 weeks at time of randomization.)
• Adequate liver function as shown by:
• serum bilirubin ≤ 1.5 x ULN
• ALT and AST ≤ 2.5x ULN (≤ 5x ULN in patients with liver metastases)
• Written informed consent according to local guidelines.

Exclusion criteria

• Change of one or more antiepileptic medication in the past 6 months.
• Prior exposure to the systemic use of an mTOR inhibitor.
• Exposure to any investigational agent in the 30 days prior to randomization.
• Neurosurgery within 6 months.
• Known impaired lung function (e.g.FEV1 or DLCO 2.5 x ULN or serum bilirubin > 1.5 x ULN, hemoglobin 1.5 x ULN.
• Uncontrolled hyperlipidemia: Fasting serum cholesterol > 300 mg/dL OR > 7.75 mmol/L AND Fasting triglycerides > 2.5 x ULN.
• Uncontrolled diabetes mellitus as defined by fasting serum glucose > 1.5 x ULN.
• Patients with bleeding diathesis or on oral anti-vitamin K medication (except low dose warfarin).
• Patients with known history of HIV seropositivity.
• Pregnancy or breast feeding.
• Active infection at date of randomization.
• Prior history of organ transplant.
• Recent surgery (involving entry into a body cavity or requiring sutures) within the 4 weeks prior to randomization.
• Inability to attend scheduled clinic visits.
• History of malignancy in the past two years, other than squamous or basal cell skin cancer.
• Patients should not receive immunization with attenuated live vaccines within one month of study entry or during study period. Close contact with those who have received attenuated live vaccines should be avoided during treatment with everolimus. Examples of live vaccines include intranasal influenza, measles, mumps, rubella, oral polio, BCG, yellow fever, varicella and TY21a typhoid vaccines.
• Liver disease such as cirrhosis or severe hepatic impairment (Child-Pugh class C).

Note: A detailed assessment of Hepatitis B/C medical history and risk factors must be done at screening for all patients. HBV DNA and HCV RNA PCR testing are required at screening for all patients with a positive medical history based on risk factors and/or confirmation of prior HBV/HCV infection.

• Patients receiving chronic, systemic treatment with corticosteroids or another immunosuppressive agent. Topical or inhaled corticosteroids are allowed.
• Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study such as:
• symptomatic congestive heart failure of New York heart Association Class III or IV
• unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction within 6 months of start of study drug, serious uncontrolled cardiac arrhythmia or any other clinically significant cardiac disease
• Patients who have received an IQ score under