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ACTIVE NOT RECRUITING Phase 2

A Study to Evaluate XEN1101 as Adjunctive Therapy in Focal Epilepsy

NCT03796962 · View on ClinicalTrials.gov ↗

Study Summary

The XEN1101 Phase 2 clinical trial is a randomized, double-blind, placebo-controlled study that will evaluate the clinical efficacy, safety and tolerability of increasing doses of XEN1101 administered as adjunctive treatment in adult patients diagnosed with focal epilepsy, followed by an optional open-label extension (OLE).

Conditions Studied

Interventions

  • DRUG XEN1101

Study Locations (20)

Florida

  • University of Florida Jacksonville — Jacksonville
  • Mayo Clinic Florida — Jacksonville
  • Visionary Investigators Network — Miami
  • Don Clinical Research Center — Miami
  • The Neurology Research Group, LLC. — Miami
  • Research Institute of Orlando, LLC — Orlando
  • Medsol Clinical Research Center — Port Charlotte
  • Tallahassee Neurological Clinic — Tallahassee
  • University of South Florida — Tampa

Alabama

  • University of Alabama at Birmingham — Birmingham
  • Strada Patient Care Center — Mobile

California

  • Altman Clinical Translational Research Institute (ACTRI) — La Jolla
  • California Pacific Medical Center (CPMC) - Sutter Pacific Epilepsy Program — San Francisco

Arizona

  • Xenoscience, Inc. — Phoenix

Arkansas

  • Clinical Trials, Inc. — Little Rock

Colorado

  • University of Colorado Hospital Anschutz Outpatient Pavilion — Aurora

Georgia

  • Georgia Neurology and Sleep Medicine Associate — Suwanee

Hawaii

  • Hawaii Pacific Neuroscience — Honolulu

Trial Details

FieldValue
Enrollment Target 325 participants
Start Date 2019-01-30
Est. Completion 2028-10
Phase Phase 2

Sponsor

Xenon Pharmaceuticals

8 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03796962

The ClinicalTrials.gov registry entry for NCT03796962 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 325 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Xenon Pharmaceuticals, which has 8 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Focal Epilepsy appearing as the primary indexed condition, and to 1 intervention — of which XEN1101 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03796962 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Florida, Alabama, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03796962 about?

NCT03796962 is a clinical study titled "A Study to Evaluate XEN1101 as Adjunctive Therapy in Focal Epilepsy". The XEN1101 Phase 2 clinical trial is a randomized, double-blind, placebo-controlled study that will evaluate the clinical efficacy, safety and tolerability of increasing doses of XEN1101 administered as adjunctive treatment in adult patients diagnosed with focal epilepsy, followed by an optional op...

What is the current status of trial NCT03796962?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 325 participants. The study started on 2019-01-30. Estimated completion is 2028-10.

What conditions does trial NCT03796962 study?

This clinical trial studies the following conditions: Focal Epilepsy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03796962?

The interventions under investigation include: XEN1101 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03796962?

This trial is sponsored by Xenon Pharmaceuticals, which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03796962 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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