A Phase 1/2 Study of NRTX-1001 Neuronal Cell Therapy in Drug-Resistant Bilateral Mesial Temporal Lobe Epilepsy (MTLE)
Recruiting · NCT06422923 · Interventional (participants receive a specific treatment) · Lead sponsor: Neurona Therapeutics
View the official record on ClinicalTrials.gov →Interventions studied
NRTX-1001
What this trial is about
This is a multicenter, single arm, open label clinical trial that is designed to test the safety and preliminary efficacy of single administration inhibitory nerve cells called interneurons (NRTX-1001), into both temporal lobes of subjects with drug-resistant bilateral mesial temporal lobe epilepsy.
Who can take part
Age range
18 Years to 75 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 1, Phase 2
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Male or female, age 18-75 years.
- Subjects of childbearing potential will use highly effective contraception.
- Proven history of focal seizures of hippocampal origin with bilateral seizure foci confirmed by scalp or intracranial ictal EEG (including confirmation by recordings from responsive neurostimulation \[RNS\] electrodes when applicable).
- Either
- bilateral hippocampal sclerosis on MRI (evidenced by increased FLAIR signal intensity in both hippocampi or by visual assessment showing reduced volume compared to normal) or
- bilateral temporal hypometabolism on 18-Flourodeoxyglucose Positron Emission Tomography (FDG PET) (assessed by visual assessment, comparing temporal regions to frontal/parietal lobe neocortex). In this case, ictal EEG recordings must also include intracranial confirmation.
- a combination of unilateral instances of the evidence described in a. and b. (e.g., one side can be evidenced by criterion a. and the other side by criterion b.) MRI or PET scans used for assessment must have been acquired within 3 years of screening.
- Subject has had at least four clinical focal seizures, including at least two clinical focal seizures with objective manifestations, on average, per month for the 6 months prior to screening.
- Subject has previously had adequate (in opinion of investigator) therapeutic trials of at least two Anti-Seizure Medicines (ASMs).
- Current ASM regimen, and doses of other drugs known to affect seizure frequency (e.g., antidepressants), have been stable for at least three months prior to enrollment.
- Subject can converse and read in English or Spanish. Able to participate in required study procedures and provide signed informed consent.
- Key
Exclusion criteria
- Epilepsy due to other and/or progressive neurologic disease.
- Evidence of seizure focus outside hippocampus (either by seizure semiology or EEG findings).
- MRI indicating potential malignant lesion (low-grade glioma of any type is excluded) in any location or non-malignant potentially epileptogenic lesion outside the hippocampus. Small (\<2 cm) non invasive meningioma, remote from the affected temporal lobe, is not exclusionary.
- Seizures of non-focal origin.
- History of status epilepticus in the year prior to screening, as guided by ILAE criteria (Trinka 2015) in the judgement of the PI. A history of cluster seizures is permitted.
- Psychogenic Non-Epileptic Seizures (PNES) within the past 3 years.
- Severe psychiatric disorders.
- Primary or secondary immunodeficiency.
- Pregnancy, or currently breastfeeding.
- Suicide attempts in past year.
- Significant other medical conditions which would impair safe participation.
Where it is running
17 locations listed across 11 US states.
- University of Arkansas for Medical Sciences - Little Rock, Arkansas, United States
- University of Southern California Keck Hospital - Los Angeles, California, United States
- UC Irvine Medical Center - Orange, California, United States
- Stanford University - Palo Alto, California, United States
- University of California San Diego - San Diego, California, United States
- University of California San Francisco - San Francisco, California, United States
- University of Colorado Anschutz Medical Campus - Aurora, Colorado, United States
- University of Chicago - Chicago, Illinois, United States
- University of Iowa Health Care - Iowa City, Iowa, United States
- SUNY Upstate Medical University - Syracuse, New York, United States
- Atrium Health - Charlotte, North Carolina, United States
- Duke University Hospital - Durham, North Carolina, United States
- Wake Forest Baptist Medical Center - Winston-Salem, North Carolina, United States
- Oregon Health and Science University - Portland, Oregon, United States
- UTHealth Houston - Houston, Texas, United States
- UVA Health University Medical Center - Charlottesville, Virginia, United States
- Medical College of Wisconsin - Milwaukee, Wisconsin, United States