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COMPLETED Phase 2

Efficacy of YKP3089 in Patients With Photosensitive Epilepsy

NCT00616148 · View on ClinicalTrials.gov ↗

Study Summary

The aim of this study is to evaluate the ability of a single oral dose of YKP3089 to abolish or clearly reduce the IPS-induced photo-paroxysmal EEG response in photosensitive epilepsy patients, and to measure the onset and duration of the effect. Several cohorts will be used, to sequentially investigate different doses.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG YKP3089

Study Locations (4)

New York

  • Cornell Medical Center — New York
  • Montefiore Medical Center — The Bronx

Maryland

  • Johns Hopkins Medical Center — Baltimore

Pennsylvania

  • University of Pennsylvania Epilepsy Center — Philadelphia

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2007-08
Est. Completion 2010-01
Phase Phase 2

Sponsor

SK Life Science

9 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00616148

The ClinicalTrials.gov registry entry for NCT00616148 describes a study currently listed as completed. 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 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is SK Life Science, which has 9 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 Epilepsy appearing as the primary indexed condition, and to 2 interventions — of which Placebo 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: NCT00616148 reports 4 study locations spanning 3 distinct geographic areas — top geographies include New York, Maryland, Pennsylvania. 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 NCT00616148 about?

NCT00616148 is a clinical study titled "Efficacy of YKP3089 in Patients With Photosensitive Epilepsy". The aim of this study is to evaluate the ability of a single oral dose of YKP3089 to abolish or clearly reduce the IPS-induced photo-paroxysmal EEG response in photosensitive epilepsy patients, and to measure the onset and duration of the effect. Several cohorts will be used, to sequentially investi...

What is the current status of trial NCT00616148?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2007-08. Estimated completion is 2010-01.

What conditions does trial NCT00616148 study?

This clinical trial studies the following conditions: 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 NCT00616148?

The interventions under investigation include: Placebo (DRUG), YKP3089 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00616148?

This trial is sponsored by SK Life Science, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00616148 being conducted?

This trial has 4 study locations across Maryland, New York, Pennsylvania. 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