Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05135091

Study of NRTX-1001 Neural Cell Therapy in Drug-Resistant Unilateral Mesial Temporal Lobe Epilepsy (EPIC (EPIlepsy Cell Therapy))

This clinical trial is designed to test whether a single image-guided intracerebral administration of inhibitory nerve cells, called interneurons (NRTX-1001), into subjects with drug-resistant unilateral mesial temporal lobe epilepsy (MTLE), with or without mesial temporal sclerosis (MTS), is safe (frequency of adverse events) and effective (seizure frequency). NRTX-1001 comprises human interneurons that secrete a neurotransmitter, gamma-aminobutyric acid (GABA).

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University of Alabama, Birmingham, Alabama, United States

Loading trial locations.

About this study

Subjects will undergo a single CT or MRI-guided intracerebral administration of human interneurons that secrete the inhibitory neurotransmitter, gamma-aminobutyric acid (GABA), into the temporal lobe region of the brain where the seizures are thought to arise. NRTX-1001 is intended to suppress the onset and spread of seizures. Safety, efficacy, tolerability, and effects on reducing seizure frequency and epilepsy disease symptoms will be assessed at regular 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 5, and then annual visits in years 6 through 15. Subjects will be placed on an immunosuppressant medication regimen for a duration of one year to partially suppress the subjects' immune system to promote the intended long-term persistence of NRTX-1001. This immunosuppressant medication is intended to be discontinued after the first year; however, the NRTX-1001 cells are intended to persist long-term.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • Male or Female, age ≥18 to ≤75
  • Focal seizures, clinically defined as unilateral MTLE
  • Has failed to achieve seizure control despite adequate trials of at least 2 ASDs at appropriate doses
  • Currently on stable doses (at least 1 month prior to Screening) of approved ASDs
  • Single seizure focus confirmed within one hippocampus
  • Seizure frequency averages ≥4 per 28-day period, including at least 2 clinical focal seizures per 28-day period with objective manifestations or more severe types, over the 6 months prior to the Screening Visit. (Phase 1/2 only)
  • Disabling seizure frequency of ≥2 per 28-day period averaged over 3 months prior to the Screening visit and over a prospective 10-week baseline period prior to Randomization (Phase 3 Only)

Key Exclusion Criteria:

  • Epilepsy due to other medical conditions and/or progressive neurologic disease
  • Evidence of seizure focus outside of the hippocampus or evidence of seizures of non- focal origin.
  • Significant other medical conditions which would impair safe participation
  • History of status epilepticus in the 3 years prior to screening.
  • Primary or secondary immunodeficiency
  • Suicide attempts in the past year 3 years
  • Severe psychiatric disorders
  • Prior lobectomy or LITT procedure
  • MRI indicating potential malignant lesion
  • Pregnancy, or currently breastfeeding.

Treatment and study plan

NRTX-1001

Biological

Biological: NRTX-1001 is an experimental neural cell therapy product candidate derived from an allogeneic human embryonic stem cell line. The stem cells were converted into inhibitory nerve cells that produce GABA.

Other names: GABA-secreting interneurons

Sham Comparator

Procedure

Sham Comparator

Primary outcomes

  1. Frequency of serious or severe AEs (Phase 1/2)

    Time frame: 1 year

    The primary endpoint of the study is the frequency of serious or severe AEs over the period of 1 year after administration.

  2. Change in disabling seizure frequency (Phase 3)

    Time frame: 4-6 months after surgery

    The difference in median percent change from baseline in diary-reported disabling seizure frequency (seizures per 28 days) between subjects that receive NRTX-1001 and those who receive sham treatment.

Secondary outcomes

  1. Responder rate (Phase 3)

    Time frame: 4-6 months after surgery

    The difference in the 50% responder rate, e.g., the difference between the fraction of subjects who receive NRTX-1001 and those that receive sham treatment who experience at least a 50% reduction from baseline in disabling seizure frequency.

  2. Responder rate (Phase 3)

    Time frame: 4-6 months after surgery

    The difference in the 75% responder rate, e.g., the difference between the fraction of subjects who receive NRTX-1001 and those that receive sham treatment who experience at least a 75% reduction from baseline in disabling seizure frequency.

Study contacts

Contact information is provided by the study sponsor or research team.

Eduardo Dunayevich, MD

CONTACT

[email protected]

650-436-3045

Neurona MedInfo

CONTACT

[email protected]

650-580-3825

Sponsors and collaborators

Lead sponsor

Neurona Therapeutics

Industry

Collaborators

  • California Institute for Regenerative Medicine (CIRM)

Registry information

Official study title

A Study of Inhibitory Interneurons (NRTX-1001) in Drug-Resistant Unilateral Mesial Temporal Lobe Epilepsy (MTLE)

Acronym: EPIC

Important dates

Study start
2022
Primary completion
2029
Study completion
2043
First posted
Nov 26, 2021
Registry last updated
Jun 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.