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Not listed Phase 3 Interventional

Safety and Effectiveness of Three Anti-HIV Drugs Combined in One Pill (Trizivir)

ClinicalTrials.gov ID: NCT00004981

Public ClinicalTrials.gov record NCT00004981. 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 Jul 23, 2026, 3:41 PM EDT

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

Official title

A Phase IIIB Randomized, Multicenter Study of the Efficacy and Safety of Combivir 1 Tablet Po Bid Plus Ziagen 300mg Po Bid Versus an Abacavir 300mg/Lamivudine 150mg/Zidovudine 300mg Combination Tablet Po Bid, Administered for 24 Weeks in Subjects With HIV-1 Infection

Study identification

NCT ID
NCT00004981
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Glaxo Wellcome
Industry
Enrollment
230 participants

Conditions and interventions

Conditions

Interventions

  • Abacavir sulfate, Lamivudine and Zidovudine Drug
  • Lamivudine/Zidovudine Drug
  • Abacavir sulfate Drug

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
12
U.S. cities
21
Facility City State ZIP Site status
AIDS Healthcare Foundation Los Angeles California 900276069
Tower Infectious Disease Med Ctr Los Angeles California 90048
Robert Scott MD Oakland California 94609
St Lukes Medical Group San Diego California 92101
Georgetown Univ Med Ctr Washington D.C. District of Columbia 20007
Whitman Walker Clinic Washington D.C. District of Columbia 20009
Univ of Miami School of Medicine Miami Florida 33136
Specialty Med Care Ctrs of South Florida Inc Miami Florida 33142
Saint Josephs Comprehensive Research Institute Tampa Florida 33607
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612
New England Med Ctr Boston Massachusetts 02111
Research Med Ctr Kansas City Missouri 64111
Addiction Research and Treatment Corp Brooklyn New York 11201
Saint Vincent's Hosp and Med Ctr New York New York 10011
St Luke Roosevelt Hosp New York New York 10011
Lehigh Valley Hosp Allentown Pennsylvania 18105
Hahnemann Univ Hosp Philadelphia Pennsylvania 191021192
Anderson Clinical Research Pittsburgh Pennsylvania 15213
Burnside Clinic Columbia South Carolina 29206
Univ of Tennessee Memphis Tennessee 38163
Nashville Health Management Foundation / Vanderbilt Univ Nashville Tennessee 37203
Nicholas Bellos Dallas Texas 75246
Univ of Texas Med Branch Galveston Texas 77555
Therapeutic Concepts Houston Texas 77004

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 NCT00004981, 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 Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00004981 live on ClinicalTrials.gov.

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