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NCT00410371 · ClinicalTrials.gov registry record · Phase 1

Study to Compare Two Formulations of Lamotrigine in Healthy Subjects

A Phase 1 study of Mental Disorders, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
96
Enrollment target
1
Study location

NCT00410371: Completed Phase 1 study of Mental Disorders, sponsored by GlaxoSmithKline.

NCT00410371 is a Phase 1 study of Mental Disorders that has completed, run by GlaxoSmithKline. The registered enrollment target is 96 participants, below the 681-participant average among 25 other Mental Disorders trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00410371, a Phase 1 study of Mental Disorders, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
96 participants
Enrollment target
1
Study location

Study Summary

This study intends to compare the pharmacokinetic characteristics, safety and tolerability of two formulations of lamotrigine in healthy male and female volunteers

Conditions Studied

Interventions

  • DRUG Lamotrigine
  • DRUG GI267119

Study Locations (1)

Nebraska

  • GSK Investigational Site - Lincoln

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2006-12-28
Est. Completion 2007-01-25
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT00410371 record still lists

NCT00410371 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 96 participants, a relatively small participant target, below the 681-participant average among 25 other Mental Disorders trials with a reported enrollment target (86% lower).

The record links to 1 condition, with Mental Disorders appearing as the primary indexed condition, and to 2 interventions - of which Lamotrigine is the first listed.

NCT00410371 reports a single indexed study location in Nebraska.

Frequently Asked Questions

What is clinical trial NCT00410371 about?

NCT00410371 is a clinical study titled "Study to Compare Two Formulations of Lamotrigine in Healthy Subjects". This study intends to compare the pharmacokinetic characteristics, safety and tolerability of two formulations of lamotrigine in healthy male and female volunteers

What is the current status of trial NCT00410371?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 96 participants. The study started on 2006-12-28. Estimated completion is 2007-01-25.

What conditions does trial NCT00410371 study?

This clinical trial studies the following conditions: Mental Disorders.

What interventions are being tested in trial NCT00410371?

The interventions under investigation include: Lamotrigine (DRUG), GI267119 (DRUG).

Who is sponsoring clinical trial NCT00410371?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00410371 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Mental Disorders

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00410371's enrollment target sits among peer trials

96 18th of 25 higher than 8 of 25 other Mental Disorders trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Mental Disorders trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00410371, the US trial registry maintained by the National Library of Medicine. NCT00410371 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.