A Phase 1/2 Study of NRTX-1001 Neuronal Cell Therapy in Drug-Resistant Bilateral Mesial Temporal Lobe Epilepsy (MTLE)
Neurona Therapeutics · NCT06422923
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 1, Phase 2
- Target enrollment
- 10
- US sites recruiting
- 16
- Study start
- November 14, 2024
- Record last updated
- January 7, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study 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.
Being studied: NRTX-1001
Conditions: Epilepsy, Temporal Lobe
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Key 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.
or
- 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.
Recruiting US locations
University of Arkansas for Medical Sciences
Little Rock, AR 72205
Site contact: Shellah Rogers, Nurse · 501-398-8622 · Scrogers2@uams.edu
University of Southern California Keck Hospital
Los Angeles, CA 90033
Site contact: Zoe B Durkin, SC · 323-422-6625 · zoe.durkin@med.usc.edu
UC Irvine Medical Center
Orange, CA 92868
Site contact: UCI Alpha Clinic · 949-824-3990
Stanford University
Palo Alto, CA 94304
Site contact: Jordan Seliger, CRC, MA · 650-460-9260 · jseliger@stanford.edu
University of California San Diego
San Diego, CA 92037
Site contact: Mateo Santizo, CRC · (858)583-0929 · msantizo@health.ucsd.edu
University of Colorado Anschutz Medical Campus
Aurora, CO 80045
Site contact: Pamela D Gerecht, Ph.D. SC · 303-724-4134 · pamela.davidgerecht@cuanschutz.edu
University of Chicago
Chicago, IL 60637
Site contact: Agnieszka Stadnik, MS · 773-702-8996 · astadnik@bsd.uchicago.edu
University of Iowa Health Care
Iowa City, IA 52242
Site contact: Loraine Brenner, MSN · 319-356-4361 · loraine-brenner@uiowa.edu
SUNY Upstate Medical University
Syracuse, NY 13210
Site contact: Lena F Deb, BA · 315-464-9756 · debl@upstate.edu
Atrium Health
Charlotte, NC 28204
Site contact: Dianelis Diaz, RN, BSN, CRC · 704-446-1900 · dianelis.diaz@atriumhealth.org
Duke University Hospital
Durham, NC 27710
Site contact: Hazani Benitez-Rosas · 919-681-4974 · Hazani.benitez-rosas@duke.edu
Wake Forest Baptist Medical Center
Winston-Salem, NC 27157
Site contact: Carolyn W Hedrick, RMA, CCRP · 336-716- 8694 · Carolyn.Hedrick@AdvocateHealth.org
Oregon Health and Science University
Portland, OR 97239
Site contact: Claire Dorfman, BA · 971-413-9201 · dorfman@ohsu.edu
UTHealth Houston
Houston, TX 77030
Site contact: Eliana M Klier, PhD · 713-500-5442 · Eliana.Klier@uth.tmc.edu
UVA Health University Medical Center
Charlottesville, VA 22903
Site contact: Kimberlee E Meegan, BS, CRC III · 434-243-2040 · dxh5dv@uvahealth.org
Medical College of Wisconsin
Milwaukee, WI 53226
Site contact: Sarah Young, MS · 414-955-0989 · scyoung@mcw.edu
Study contacts (from the official record)
- Neurona MedInfo · 650-580-3825 · neuronamedinfo@neuronatx.com
- Eduardo Dunayevich, MD · 650-436-3045 · edunayevich@neuronatx.com
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