Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00002251 · ClinicalTrials.gov registry record · NA

A Multiple Dose Crossover Pharmacokinetics Study to Evaluate the Effects of Food on the Absorption of Oral Ganciclovir

A NA study, sponsored by Hoffmann-La Roche.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT00002251: Completed NA study, sponsored by Hoffmann-La Roche.

NCT00002251 is a NA study that has completed, run by Hoffmann-La Roche. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00002251, a NA study, has completed, sponsored by Hoffmann-La Roche.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

This study is designed to determine the influence of food on the absorption and relative bioavailability of oral ganciclovir by comparing the absorption of oral ganciclovir in a fed and fasting state at steady state plasma levels.

Interventions

  • DRUG Ganciclovir

Trial Details

FieldValue
Enrollment Target 20 participants
Phase NA
Hoffmann-La Roche

909 total trials

What the finished NCT00002251 record still lists

NCT00002251 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Ganciclovir is the first listed.

NCT00002251 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00002251 about?

NCT00002251 is a clinical study titled "A Multiple Dose Crossover Pharmacokinetics Study to Evaluate the Effects of Food on the Absorption of Oral Ganciclovir". This study is designed to determine the influence of food on the absorption and relative bioavailability of oral ganciclovir by comparing the absorption of oral ganciclovir in a fed and fasting state at steady state plasma levels.

What is the current status of trial NCT00002251?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants.

What interventions are being tested in trial NCT00002251?

The interventions under investigation include: Ganciclovir (DRUG).

Who is sponsoring clinical trial NCT00002251?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00002251's enrollment target sits among peer trials

20 1768th of 2000 higher than 140 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Source: ClinicalTrials.gov NCT00002251, the US trial registry maintained by the National Library of Medicine. NCT00002251 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.