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NCT00868361 · ClinicalTrials.gov registry record · Phase 1

A Study to Investigate the Absorption, Metabolism and Excretion of Talampanel

A Phase 1 study, sponsored by Teva Branded Pharmaceutical Products R&D.

Terminated
Registry status
Phase 1
Development phase
10
Enrollment target

NCT00868361: Clinical Trial Phase 1 study, sponsored by Teva Branded Pharmaceutical Products R&D.

NCT00868361 is a Phase 1 study that was terminated before completion, run by Teva Branded Pharmaceutical Products R&D. The registered enrollment target is 10 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00868361, a Phase 1 study, was terminated before completion, sponsored by Teva Branded Pharmaceutical Products R&D.

TERMINATED
Registry status
Phase 1
Development phase
10 participants
Enrollment target

Study Summary

The purpose of this study is to characterize the chemical breakdown and excretion of talampanel and its break down products in plasma, feces, and urine of healthy human volunteers.

Interventions

  • DRUG Talampanel (non-radiolabeled), [14C] Talampanel

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2009-05
Est. Completion 2009-09
Phase Phase 1

Why NCT00868361 stopped before completion

NCT00868361 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 1 intervention - of which Talampanel (non-radiolabeled), [14C] Talampanel is the first listed.

NCT00868361 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00868361 about?

NCT00868361 is a clinical study titled "A Study to Investigate the Absorption, Metabolism and Excretion of Talampanel". The purpose of this study is to characterize the chemical breakdown and excretion of talampanel and its break down products in plasma, feces, and urine of healthy human volunteers.

What is the current status of trial NCT00868361?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2009-05. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00868361?

The interventions under investigation include: Talampanel (non-radiolabeled), [14C] Talampanel (DRUG).

Who is sponsoring clinical trial NCT00868361?

This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 167 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00868361's enrollment target sits among peer trials

10 1913th of 2000 higher than 46 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00868361, the US trial registry maintained by the National Library of Medicine. NCT00868361 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.