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NCT00002118 · ClinicalTrials.gov registry record · NA

An Open-Label Safety Program for the Use of Zalcitabine (Dideoxycytidine; ddC) in Pediatric Patients With Symptomatic HIV Infection Who Have Failed or Are Intolerant to AZT Monotherapy, or Who Have Completed Other ddC Protocols, or Are Ineligible for Other Ongoing Clinical Studies

A NA study, sponsored by Hoffmann-La Roche.

Completed
Registry status
NA
Development phase
600
Enrollment target

NCT00002118: Completed NA study, sponsored by Hoffmann-La Roche.

NCT00002118 is a NA study that has completed, run by Hoffmann-La Roche. The registered enrollment target is 600 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00002118, a NA study, has completed, sponsored by Hoffmann-La Roche.

COMPLETED
Registry status
NA
Development phase
600 participants
Enrollment target

Study Summary

To allow, on a compassionate use basis, zalcitabine (ddC) for pediatric patients with symptomatic HIV disease who have failed treatment or who are intolerant to zidovudine (AZT), or who have completed other ddC protocols, or who are ineligible for ongoing clinical trials.

Interventions

  • DRUG Zalcitabine

Trial Details

FieldValue
Enrollment Target 600 participants
Phase NA
Hoffmann-La Roche

909 total trials

What the finished NCT00002118 record still lists

NCT00002118 is an interventional study that assigns participants to a tested intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (57% lower).

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

NCT00002118 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00002118 about?

NCT00002118 is a clinical study titled "An Open-Label Safety Program for the Use of Zalcitabine (Dideoxycytidine; ddC) in Pediatric Patients With Symptomatic HIV Infection Who Have Failed or Are Intolerant to AZT Monotherapy, or Who Have Completed Other ddC Protocols, or Are Ineligible for Other Ongoing Clinical Studies". To allow, on a compassionate use basis, zalcitabine (ddC) for pediatric patients with symptomatic HIV disease who have failed treatment or who are intolerant to zidovudine (AZT), or who have completed other ddC protocols, or who are ineligible for ongoing clinical trials.

What is the current status of trial NCT00002118?

This trial is currently completed. It is a NA study. The enrollment target is 600 participants.

What interventions are being tested in trial NCT00002118?

The interventions under investigation include: Zalcitabine (DRUG).

Who is sponsoring clinical trial NCT00002118?

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 NCT00002118's enrollment target sits among peer trials

600 162nd of 2000 higher than 1,827 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

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Source: ClinicalTrials.gov NCT00002118, the US trial registry maintained by the National Library of Medicine. NCT00002118 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.