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NCT00002299 · ClinicalTrials.gov registry record · NA

The Safety and Effectiveness of Ganciclovir Plus Interferon Beta in Preventing the Return of Cytomegalovirus (CMV) of the Eyes in Patients With AIDS

A NA study, sponsored by Hoffmann-La Roche.

Completed
Registry status
NA
Development phase

NCT00002299 is a NA study that has completed, run by Hoffmann-La Roche.

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The verdict

NCT00002299, a NA study, has completed, sponsored by Hoffmann-La Roche.

COMPLETED
Registry status
NA
Development phase

Study Summary

The use of ganciclovir (DHPG) in combination with interferon beta to prevent relapse of cytomegalovirus retinitis in patients with AIDS. While early clinical trials have shown that 30 mg/kg/week of DHPG is usually sufficient to delay or prevent relapse, neutropenia is a common dose-limiting problem in about 50 percent of patients. Since in vitro data have suggested that there is synergism between DHPG and interferon beta against cytomegalovirus, a reduced dose of DHPG in combination with a low dose of interferon beta may prevent relapse without causing neutropenia. If remission can be maintained with low-dose DHPG and interferon beta, maintenance therapy with a moderate dose of interferon beta alone will be evaluated in a subsequent protocol.

Interventions

  • DRUG Ganciclovir
  • DRUG Interferon beta-1b

Trial Details

FieldValue
Phase NA

Sponsor

Hoffmann-La Roche

909 total trials

What the Registry Record Tells You About NCT00002299

The ClinicalTrials.gov registry entry for NCT00002299 describes a study currently listed as completed, categorized as NA. An enrollment target was not published in the registry record, which is common for early-stage or observational entries. The listed sponsor is Hoffmann-La Roche, which has 909 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Ganciclovir is the first listed.

NCT00002299 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00002299 about?

NCT00002299 is a clinical study titled "The Safety and Effectiveness of Ganciclovir Plus Interferon Beta in Preventing the Return of Cytomegalovirus (CMV) of the Eyes in Patients With AIDS". The use of ganciclovir (DHPG) in combination with interferon beta to prevent relapse of cytomegalovirus retinitis in patients with AIDS. While early clinical trials have shown that 30 mg/kg/week of DHPG is usually sufficient to delay or prevent relapse, neutropenia is a common dose-limiting problem ...

What is the current status of trial NCT00002299?

This trial is currently completed. It is a NA study.

What interventions are being tested in trial NCT00002299?

The interventions under investigation include: Ganciclovir (DRUG), Interferon beta-1b (DRUG).

Who is sponsoring clinical trial NCT00002299?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.