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Completed Phase 2 Interventional

An Open-Label, Multicenter Study to Evaluate the Safety and Tolerability of Dideoxycytidine (ddC) in Patients With AIDS or Advanced ARC Who Previously Demonstrated Intolerance to Zidovudine (AZT) in Protocol N3300 or N3492

ClinicalTrials.gov ID: NCT00002265

Public ClinicalTrials.gov record NCT00002265. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 19, 2026, 6:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT00002265
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
Not listed

Conditions and interventions

Conditions

Interventions

  • Zalcitabine Drug

Drug

Eligibility (public fields only)

Age range
13 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 23, 2005

United States locations

U.S. sites
9
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
Davies Med Ctr San Francisco California 94114
Mount Zion Med Ctr San Francisco California 94115
Ctr for Special Immunology Fort Lauderdale Florida 33308
Dr Robert Swartz Fort Myers Florida 33901
Med Service Miami Florida 33125
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
Henry Ford Hosp Detroit Michigan 48202
Graduate Hosp Philadelphia Pennsylvania 19146
Humana Hosp / Med City Dallas Dallas Texas 75230

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002265, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 23, 2005 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002265 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →