Recruiting
Phase 1
Phase 2

NRTX-1001

Sponsor:

Neurona Therapeutics

Code:

NCT06422923

Conditions

Epilepsy, Temporal Lobe

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

NRTX-1001

Study Details

Brief 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.

Conditions

Epilepsy, Temporal Lobe

Study ID

NCT06422923

Start date

Nov 14, 2024

Status verified date

Jan, 2026

Completion date

Jun 15, 2042

Anticipated

Primary completion date

Jun 15, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

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 foci confirmed by scalp or intracranial ictal EEG (including confirmation by recordings from responsive neurostimulation \[RNS\] electrodes when applicable).
4. Either

1. 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
2. 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
3. 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.
5. 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.
6. Subject has previously had adequate (in opinion of investigator) therapeutic trials of at least two Anti-Seizure Medicines (ASMs).
7. 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.
8. Subject can converse and read in English or Spanish. Able to participate in required study procedures and provide signed informed consent.

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 EEG findings).
3. 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.
4. Seizures of non-focal origin.
5. 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.
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

Enrollment

10 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Treatment Arm

This is an open-label study of the bilateral intrahippocampal administration of NRTX-1001 in a single dose cohort of up to 10 subjects with drug-resistant bilateral MTLE.

Interventions

NRTX-1001

Biological: NRTX-1001 is an inhibitory neural cell therapy investigational product. It is derived from a human stem cell line that has been converted into high-purity inhibitory interneurons that produce GABA. NRTX-1001 is intended to persist long-term and not require repeated administration.

Primary outcome measure

  • Incidence of Serious Adverse Events at end of month 12 [ Time Frame: 12 months after treatment ]

Central Contacts and Locations

Central contacts

Locations

University of Arkansas for Medical Sciences

Recruiting

Little Rock, Arkansas, United States, 72205

Contacts

Shellah Rogers, Nurse

501-398-8622Scrogers2@uams.edu

Principal Investigator:

Sisira Yadala, MD

University of Southern California Keck Hospital

Recruiting

Los Angeles, California, United States, 90033

Contacts

Principal Investigator:

Charles Y Liu, MD, PhD

UC Irvine Medical Center

Recruiting

Orange, California, United States, 92868

Contacts

UCI Alpha Clinic

949-824-3990

Principal Investigator:

Mona Sazgar, MD

Stanford University

Recruiting

Palo Alto, California, United States, 94304

Contacts

Jordan Seliger, CRC, MA

650-460-9260jseliger@stanford.edu

Principal Investigator:

Kevin Graber, MD

University of California San Diego

Recruiting

San Diego, California, United States, 92037

Contacts

Principal Investigator:

Jerry J Shih, MD

University of Colorado Anschutz Medical Campus

Recruiting

Aurora, Colorado, United States, 80045

Contacts

Principal Investigator:

Steven Ojemann, MD

University of Chicago

Recruiting

Chicago, Illinois, United States, 60637

Contacts

Principal Investigator:

Peter Warnke, MD

University of Iowa Health Care

Recruiting

Iowa City, Iowa, United States, 52242

Contacts

Principal Investigator:

Mark Granner, MD

SUNY Upstate Medical University

Recruiting

Syracuse, New York, United States, 13210

Contacts

Principal Investigator:

Shahram Izadyar, MD

Atrium Health

Recruiting

Charlotte, North Carolina, United States, 28204

Contacts

Principal Investigator:

Rajdeep Singh, MD

Duke University Hospital

Recruiting

Durham, North Carolina, United States, 27710

Contacts

Principal Investigator:

Derek Southwell, MD, PhD

Wake Forest Baptist Medical Center

Recruiting

Winston-Salem, North Carolina, United States, 27157

Contacts

Principal Investigator:

Gautam S Popli, MD, MBA

Oregon Health and Science University

Recruiting

Portland, Oregon, United States, 97239

Contacts

Principal Investigator:

David C Spencer, MD

UTHealth Houston

Recruiting

Houston, Texas, United States, 77030

Contacts

Principal Investigator:

Nitin Tandon, MD

UVA Health University Medical Center

Recruiting

Charlottesville, Virginia, United States, 22903

Contacts

Kimberlee E Meegan, BS, CRC III

434-243-2040dxh5dv@uvahealth.org

Principal Investigator:

Nathan Fountain, MD

Medical College of Wisconsin

Recruiting

Milwaukee, Wisconsin, United States, 53226

Contacts

Principal Investigator:

Sean Lew, MD

More Information

Sponsor

Neurona Therapeutics

Last update posted

Jan 7, 2026

Last verified

Jan, 2026

Keywords

  • Bilateral Temporal Lobe Epilepsy
  • Bilateral MTLE
  • Refractory Bilateral MTLE

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Neurona Therapeutics on 2026-01-07.