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NCT06063850 · ClinicalTrials.gov registry record · Phase 1

AMT-260 Gene Therapy Study in Adults With Unilateral Refractory Mesial Temporal Lobe Epilepsy

A Phase 1 study of Mesial Temporal Lobe Epilepsy, sponsored by UniQure Biopharma B.V..

Recruiting
Registry status
Phase 1
Development phase
12
Enrollment target
18
Study locations

NCT06063850 is a Phase 1 study of Mesial Temporal Lobe Epilepsy that is actively recruiting participants, run by UniQure Biopharma B.V.. The registered enrollment target is 12 participants. The trial reports 18 study locations across 14 states.

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The verdict

NCT06063850, a Phase 1 study of Mesial Temporal Lobe Epilepsy, is actively recruiting participants, sponsored by UniQure Biopharma B.V..

RECRUITING
Registry status
Phase 1
Development phase
12 participants
Enrollment target
18
Study locations

Study Summary

The main goals of this clinical study are to learn if AMT-260 is safe and tolerable and works to reduce the frequency of seizures in adults with unilateral mesial temporal lobe epilepsy (MTLE).

Interventions

  • GENETIC AAV9-hSyn1-miGRIK2

Study Locations (18)

Maryland

  • Johns Hopkins School of Medicine - Baltimore
  • Midatlantic Epilepsy and Sleep Center - Bethesda

New Jersey

  • Northeast Regional Epilepsy Group - Hackensack
  • Robert Wood Johnson Hospital - New Brunswick

Ohio

  • Cleveland Clinic - Cleveland
  • Ohio State University - Columbus

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia
  • Allegheny Health Network - Pittsburgh

Alabama

  • University of Alabama at Birmingham - Birmingham

Arizona

  • Mayo Clinic Arizona - Phoenix

California

  • Stanford University - Palo Alto

Florida

  • Mayo Clinic Florida - Jacksonville

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2024-06-12
Est. Completion 2031-12
Phase Phase 1

Sponsor

UniQure Biopharma B.V.

4 total trials

What the Registry Record Tells You About NCT06063850

The ClinicalTrials.gov registry entry for NCT06063850 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UniQure Biopharma B.V., which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Mesial Temporal Lobe Epilepsy appearing as the primary indexed condition, and to 1 intervention - of which AAV9-hSyn1-miGRIK2 is the first listed.

NCT06063850 reports 18 study locations spanning 14 distinct geographic areas - top geographies include Maryland, New Jersey, Ohio.

Frequently Asked Questions

What is clinical trial NCT06063850 about?

NCT06063850 is a clinical study titled "AMT-260 Gene Therapy Study in Adults With Unilateral Refractory Mesial Temporal Lobe Epilepsy". The main goals of this clinical study are to learn if AMT-260 is safe and tolerable and works to reduce the frequency of seizures in adults with unilateral mesial temporal lobe epilepsy (MTLE).

What is the current status of trial NCT06063850?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2024-06-12. Estimated completion is 2031-12.

What conditions does trial NCT06063850 study?

This clinical trial studies the following conditions: Mesial Temporal Lobe Epilepsy.

What interventions are being tested in trial NCT06063850?

The interventions under investigation include: AAV9-hSyn1-miGRIK2 (GENETIC).

Who is sponsoring clinical trial NCT06063850?

This trial is sponsored by UniQure Biopharma B.V., which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06063850 being conducted?

This trial has 18 study locations across Alabama, Arizona, California, Florida, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.