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Completed Not applicable Interventional

A Multicenter, Prospective, Randomized, Double-Blind, Placebo-Controlled Trial of Three Preparations of Low-Dose Oral Alpha Interferon in HIV-Infected Patients With CD4+ Counts >= 50 and <= 350 Cells/mm3

ClinicalTrials.gov ID: NCT00000844

Public ClinicalTrials.gov record NCT00000844. 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 1, 2026, 11:11 PM 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 effects of three preparations of low-dose oral interferon alpha (i.e., Alferon LDO, Veldona, and Ferimmune) on HIV symptoms in HIV-infected patients. To evaluate differences in response to oral interferon alpha according to gender, race/ethnicity, and use of antiretrovirals. Previous or ongoing clinical trials to test the efficacy of low-dose oral interferon alpha have produced different results, and it is not clear whether the differences were due to the interferon alpha products used or to problems in the study design. Therefore, three preparations will be compared to evaluate their potential efficacies.

Study identification

NCT ID
NCT00000844
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
560 participants

Conditions and interventions

Conditions

Interventions

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
May 31, 2002
Last update posted
Nov 2, 2021

Ends 2002

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
King - Drew Med Ctr Los Angeles California 90059
AIDS Community Research Consortium Redwood City California 94063
Yale Univ / New Haven New Haven Connecticut 065102483
Med Ctr of Delaware / Wilmington Hosp Wilmington Delaware 19801
Georgetown Univ Med Ctr Washington D.C. District of Columbia 20007
Abundant Life Clinic Foundation Washington D.C. District of Columbia 20019
Howard Univ Hosp Washington D.C. District of Columbia 20059
Henry Ford Hosp Detroit Michigan 48202
Univ of Minnesota Hosp Minneapolis Minnesota 55455
SUNY / Health Sciences Ctr at Brooklyn Brooklyn New York 11203
Dr Barbara Justice New York New York 10031
Harlem AIDS Treatment Group / Harlem Hosp Ctr New York New York 10037
New York Med College / Westchester County Med Ctr Valhalla New York 10595
Univ of Pennsylvania Med Ctr Philadelphia Pennsylvania 19104
Meharry Med College Nashville Tennessee 37208

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 NCT00000844, 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 Nov 2, 2021 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00000844 live on ClinicalTrials.gov.

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