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

Last updated: April 7, 2025
Sponsor: Neurona Therapeutics
Overall Status: Active - Recruiting

Phase

1/2

Condition

Epilepsy

Seizure Disorders

Treatment

NRTX-1001

Clinical Study ID

NCT06422923
NTE002
  • Ages 18-75
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Key Inclusion Criteria:

  1. Male or female, age 18-75 years.

  2. Subjects of childbearing potential will use highly effective contraception.

  3. Proven history of focal seizures of hippocampal origin with bilateral seizure fociconfirmed by scalp or intracranial ictal EEG (including confirmation by recordingsfrom responsive neurostimulation [RNS] electrodes when applicable).

  4. Either

  5. bilateral hippocampal sclerosis on MRI (evidenced by increased FLAIR signalintensity in both hippocampi or by visual assessment showing reduced volumecompared to normal) or

  6. bilateral temporal hypometabolism on 18-Flourodeoxyglucose Positron EmissionTomography (FDG PET) (assessed by visual assessment, comparing temporal regionsto frontal/parietal lobe neocortex). In this case, ictal EEG recordings mustalso include intracranial confirmation.or

  7. 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 bycriterion b.) MRI or PET scans used for assessment must have been acquiredwithin 3 years of screening.

  8. Subject has had at least four clinical focal seizures, including at least twoclinical focal seizures with objective manifestations, on average, per month for the 6 months prior to screening.

  9. Subject has previously had adequate (in opinion of investigator) therapeutic trialsof at least two Anti-Seizure Medicines (ASMs).

  10. 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 toenrollment.

  11. Subject can converse and read in English or Spanish. Able to participate in requiredstudy procedures and provide signed informed consent.

Exclusion

Key Exclusion Criteria:

  1. Epilepsy due to other and/or progressive neurologic disease.

  2. Evidence of seizure focus outside hippocampus (either by seizure semiology or EEGfindings).

  3. MRI indicating potential malignant lesion (low-grade glioma of any type is excluded)in any location or non-malignant potentially epileptogenic lesion outside thehippocampus. Small (<2 cm) non invasive meningioma, remote from the affectedtemporal lobe, is not exclusionary.

  4. Seizures of non-focal origin.

  5. History of status epilepticus in the year prior to screening, as guided by ILAEcriteria (Trinka 2015) in the judgement of the PI. A history of cluster seizures ispermitted.

  6. Psychogenic Non-Epileptic Seizures (PNES) within the past 3 years.

  7. Severe psychiatric disorders.

  8. Primary or secondary immunodeficiency.

  9. Pregnancy, or currently breastfeeding.

  10. Suicide attempts in past year.

  11. Significant other medical conditions which would impair safe participation.

Study Design

Total Participants: 10
Treatment Group(s): 1
Primary Treatment: NRTX-1001
Phase: 1/2
Study Start date:
November 14, 2024
Estimated Completion Date:
June 15, 2042

Study Description

This is a multicenter, single arm, open-label study of NRTX-1001 in subjects with drug-resistant bilateral MTLE, with the objective of evaluating safety and preliminary efficacy in reducing seizure frequency. The subjects will undergo a single stereotactic CT or MRI-guided intracerebral administration of human interneurons into both temporal lobe regions of the brain. NRTX-1001 secretes the inhibitory neurotransmitter gamma-aminobutyric acid (GABA), which is intended to suppress the onset and spread of the seizures. Safety, tolerability, and effects on epilepsy disease symptoms will be assessed at approximately quarterly 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 15.

Connect with a study center

  • University of Arkansas for Medical Sciences

    Little Rock, Arkansas 72205
    United States

    Active - Recruiting

  • Stanford University

    Palo Alto, California 94304
    United States

    Active - Recruiting

  • University of California San Diego

    San Diego, California 92037
    United States

    Active - Recruiting

  • University of California San Francisco

    San Francisco, California 94143
    United States

    Active - Recruiting

  • University of Chicago

    Chicago, Illinois 60637
    United States

    Active - Recruiting

  • SUNY Upstate Medical University

    Syracuse, New York 13210
    United States

    Active - Recruiting

  • Duke University Hospital

    Durham, North Carolina 27710
    United States

    Active - Recruiting

  • Oregon Health and Science University

    Portland, Oregon 97239
    United States

    Active - Recruiting

  • UVA Health University Medical Center

    Charlottesville, Virginia 22903
    United States

    Active - Recruiting

  • Medical College of Wisconsin

    Milwaukee, Wisconsin 53226
    United States

    Active - Recruiting

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