New York, New York 10016


The purpose of this study is to measure if the drug called Everolimus effects mTOR signaling (an electrical activity signal in the brain) in patients with Tuberous Sclerosis Complex (TSC) and Focal Cortical Dysplasia (FCD) with treatment resistant epilepsy (TRE) who will be undergoing brain surgery. One group of patients will be treated with Everolimus, and another will not. Researchers will determine if there is a difference in mTOR signaling between the patients who were treated with Everolimus and those who were not. Previous studies have suggested that Everolimus may reduce seizure activity in TSC patients by decreasing mTOR signaling. Since patients with FCD may also have excess mTOR signaling brain activity, Everolimus may also reduce seizure activity in these patients. The drug Everolimus is approved by the Food and Drug Administration to treat specific types of breast, pancreatic, and kidney cancer, a kidney tumor called an angiomyolipoma (common in patients with TSC), and TSC patients who have a brain tumor called a subependymal giant cell astrocytoma (SEGA). However, in this research it is considered to be an investigational since it is not approved for reduction in mTOR signaling and a decrease in seizure frequency. Researchers believe that Everolimus may be useful in reducing something called cortical hyperexcitability, which is the excess brain activity that can contribute to seizures.

Study summary:

This is a single center open-label pilot clinical trial of patients with TRE, ages 1 to 40 years old, with TSC or FCD who are scheduled for epilepsy surgery. Patients will be treated with everolimus for 7 to 28 days prior to epilepsy surgery with extension of time from 7 to 28 days in successive cohorts of patients. The initial cohort of at least three patients will be treated for 7 days and after the safety of therapy is assured for this group, there will be an extension of the treatment to 14 days for at least three patients. This will be extended at one week intervals/three patient groups to a maximum treatment duration of 28 days. Resected brain tissue will be analyzed for activation of mTORC1 and mTORC2 signaling pathways, glutamatergic and GABA-ergic neurotransmission using histochemistry, genetic analysis, as well as extracellular field recordings in acute ex-vivo brain slices from surgery. A blood sample, collected at the time of surgery, will be analyzed for everolimus levels and VEGF-D. All patients will undergo standardized intra-operative ECoG recordings over the primary epileptogenic region and reviewed blindly. Subjects will be in the study for 7-28 days. The investigators will study variables listed in specific aims 1 and 2 in TSC and FCD patients treated with 7 to 28 days of everolimus and compare these to untreated control patients with TRE and TSC or FCD. A concurrent comparison group of 12 subjects will also be enrolled. They will all be undergoing routine surgery for the diagnosis of TRE with TSC or FCD. All study procedures will be performed at the Comprehensive Epilepsy Center (CEC) with the exception of the surgery, which will be performed at Tisch Hospital.


Inclusion Criteria 1. Patients: 1 year to 40 years. 2. Diagnosis: treatment resistant epilepsy due to Tuberous Sclerosis Complex or Focal Cortical Dysplasia Inclusion Criteria (Concurrent Comparison Group) 1. Patients: 1 year to 40 years. Matched for age (+/- 7 years) and sex of subjects in the treatment group. 2. Diagnosis: treatment resistant due to TSC or FCD. Matched for diagnosis of TSC and FCD. 3. Brain surgery for seizure control in which tissue is banked for research utilizing an existing IRB-approved study. Exclusion Criteria 1. Treatment with an mTOR inhibitor (everolimus, sirolimus) during the past four weeks. 2. Known hypersensitivity to an mTOR inhibitor (everolimus, sirolimus) 3. Failure to establish diagnosis of treatment resistant epilepsy (i.e., adequate trials of two appropriately-chosen, tolerated and adequate trials of antiepileptic drugs) [32]. 4. Exposure to any investigational agent in the month prior to study entry. 5. History of malignancy patients who are receiving anti-cancer treatments, such as radiation therapy and/or chemotherapy. 6. Patients with severe and/or uncontrolled medical conditions, 7. Patients on chronic corticosteroid therapy 8. A history of HIV seropositivity 9. Patients who have received live attenuated vaccines within 1 week of start of everolimus and during the study; 10. Known impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of oral everolimus; 11. Uncontrolled diabetes mellitus 12. Patients who have any severe and/or uncontrolled medical conditions 13. Known impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of oral everolimus;



Primary Contact:

Principal Investigator
Orrin Devinsky, MD
NYU Langone Health

Maria Hopkins
Phone: 646-558-0843

Backup Contact:

Sherry Ann Santarina
Phone: 646-558-0843

Location Contact:

New York, New York 10016
United States

Maria Hopkins
Phone: 646-558-0842

Site Status: Recruiting

Data Source:

Date Processed: November 18, 2019

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