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Completed Phase 3 Interventional

Phase III Randomized Double-Blind Placebo Controlled Study To Evaluate the Safety and Efficacy of Betaseron in AIDS and Advanced ARC Patients Receiving a Reduced-Dose AZT Regimen

ClinicalTrials.gov ID: NCT00002238

Public ClinicalTrials.gov record NCT00002238. 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 Sep 5, 2026, 9:03 AM EDT

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the safety and efficacy of interferon beta (Betaseron) in AIDS and advanced AIDS related complex (ARC) patients receiving a reduced-dose zidovudine (AZT) regimen.

Study identification

NCT ID
NCT00002238
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
Not listed

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
25
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Alta Bates / Herrick Hosp Berkeley California 94704
USC School of Medicine / Norris Cancer Hosp Los Angeles California 90033
Cedars Sinai Med Ctr Los Angeles California 90048
UCLA CARE Ctr Los Angeles California 90095
Summitt Med Ctr / San Francisco Gen Hosp Oakland California 94609
UCI Med Ctr Orange California 92668
Davies Med Ctr San Francisco California 94114
Santa Clara Valley Med Ctr San Jose California 95128
Dr William Davis Washington D.C. District of Columbia 20016
George Washington Univ Med Ctr Washington D.C. District of Columbia 20037
Univ of South Florida Tampa Florida 33612
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
Northwestern Univ Med School Chicago Illinois 60611
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612
Johns Hopkins Hosp Baltimore Maryland 21205
Boston Med Ctr Boston Massachusetts 02118
Beth Israel Med Ctr / Peter Krueger Clinic New York New York 10003
Chelsea Village Med Ctr New York New York 10014
Dr Douglas Dieterich New York New York 10016
Mem Sloan - Kettering Cancer Ctr New York New York 10021
Univ Hosp of Cleveland / Case Western Reserve Univ Cleveland Ohio 44106
Thomas Jefferson Med College Philadelphia Pennsylvania 19107
Saint Christopher's Hosp for Children Philadelphia Pennsylvania 191341095
Graduate Hosp Philadelphia Pennsylvania 19146
Univ TX Galveston Med Branch Galveston Texas 77550

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 NCT00002238, 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 Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002238 live on ClinicalTrials.gov.

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