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A Phase 1/2 Study of NRTX-1001 Neuronal Cell Therapy in Drug-Resistant Bilateral Mesial Temporal Lobe Epilepsy (MTLE)

Neurona Therapeutics · NCT06422923

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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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A Phase 1/2 Study of NRTX-1001 Neuronal Cell Therapy in… (NCT06422923) | Bored Studies