This clinical trial is designed to test whether a single image-guided intracerebral administration of inhibitory nerve cells, called interneurons (NRTX-1001), into subjects with drug-resistant unilateral mesial temporal lobe epilepsy (MTLE), with or without mesial temporal sclerosis (MTS), is safe (frequency of adverse events) and effective (seizure frequency). NRTX-1001 comprises human interneurons that secrete a neurotransmitter, gamma-aminobutyric acid (GABA).
Subjects will undergo a single CT or MRI-guided intracerebral administration of human interneurons that secrete the inhibitory neurotransmitter, gamma-aminobutyric acid (GABA), into the temporal lobe region of the brain where the seizures are thought to arise. NRTX-1001 is intended to suppress the onset and spread of seizures. Safety, efficacy, tolerability, and effects on reducing seizure frequency and epilepsy disease symptoms will be assessed at regular intervals for 2 years after the administration of NRTX-1001. After the two-year period, subjects will be followed with quarterly phone calls and annual visits in years 3 through 5, and then annual visits in years 6 through 15. Subjects will be placed on an immunosuppressant medication regimen for a duration of one year to partially suppress the subjects' immune system to promote the intended long-term persistence of NRTX-1001. This immunosuppressant medication is intended to be discontinued after the first year; however, the NRTX-1001 cells are intended to persist long-term.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
88
Biological: NRTX-1001 is an experimental neural cell therapy product candidate derived from an allogeneic human embryonic stem cell line. The stem cells were converted into inhibitory nerve cells that produce GABA.
Biological: NRTX-1001 is an experimental neural cell therapy product candidate derived from an allogeneic human embryonic stem cell line. The stem cells were converted into inhibitory nerve cells that produce GABA.
Sham Comparator
Mayo Clinic Arizona Epilepsy Center
Phoenix, Arizona, United States
RECRUITINGBanner-University of Arizona Medical Center Tucson Comprehensive Epilepsy Program
Tucson, Arizona, United States
RECRUITINGUniversity of Arkansas for Medical Sciences
Little Rock, Arkansas, United States
RECRUITINGUniversity of Southern California Keck Hospital
Los Angeles, California, United States
Frequency of serious or severe AEs (Phase 1/2)
The primary endpoint of the study is the frequency of serious or severe AEs over the period of 1 year after administration.
Time frame: 1 year
Change in disabling seizure frequency (Phase 3)
The difference in median percent change from baseline in diary-reported disabling seizure frequency (seizures per 28 days) between subjects that receive NRTX-1001 and those who receive sham treatment.
Time frame: 4-6 months after surgery
Responder rate (Phase 3)
The difference in the 50% responder rate, e.g., the difference between the fraction of subjects who receive NRTX-1001 and those that receive sham treatment who experience at least a 50% reduction from baseline in disabling seizure frequency.
Time frame: 4-6 months after surgery
Responder rate (Phase 3)
The difference in the 75% responder rate, e.g., the difference between the fraction of subjects who receive NRTX-1001 and those that receive sham treatment who experience at least a 75% reduction from baseline in disabling seizure frequency.
Time frame: 4-6 months after surgery
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University of California Los Angeles
Los Angeles, California, United States
RECRUITINGUC Irvine Medical Center
Orange, California, United States
RECRUITINGStanford University
Palo Alto, California, United States
RECRUITINGUniversity of California Davis
Sacramento, California, United States
RECRUITINGUniversity of California San Diego
San Diego, California, United States
RECRUITINGUniversity of California San Francisco
San Francisco, California, United States
RECRUITING...and 21 more locations