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Completed Phase 2 Interventional

A Randomized, Parallel Arm, Comparative, Open Label, Multicenter Study of the Activity and Safety of Two Formulations of Saquinavir in Combination With Other Antiretroviral Drugs

ClinicalTrials.gov ID: NCT00002162

Public ClinicalTrials.gov record NCT00002162. 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 7, 2026, 11:21 PM 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
NCT00002162
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
140 participants

Conditions and interventions

Conditions

Interventions

  • Didanosine Drug
  • Lamivudine Drug
  • Saquinavir Drug
  • Stavudine Drug
  • Zalcitabine Drug
  • Zidovudine 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
23
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Phoenix Body Positive Phoenix Arizona 85016
UCLA AIDS Clinical Research Ctr / Dept of Medicine Los Angeles California 90024
AIDS Research Ctr Palo Alto California 94304
UCD Med Ctr Sacramento California 95817
UCSD Treatment Ctr San Diego California 921036329
Mount Zion Hosp of UCSF San Francisco California 94115
San Francisco Veterans Adm Med Cntr San Francisco California 94121
Univ of Colorado Health Sciences Ctr Denver Colorado 80262
Whitman Walker Clinic Washington D.C. District of Columbia 20009
Miami Veterans Administration Med Ctr Miami Florida 33125
Saint Joseph's Hosp Tampa Florida 33614
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
Cook County Hosp Chicago Illinois 60612
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612
Tulane Univ / Tulane / LSU Clinical Trials Unit New Orleans Louisiana 70122
New England Med Ctr Boston Massachusetts 02111
Harvard Univ / Massachusetts Gen Hosp Boston Massachusetts 02114
Beth Israel Med Ctr New York New York 10003
St Vincents Hosp and Med Ctr / AIDS Cntr Progrm New York New York 10011
Univ of Oklahoma Oklahoma City Oklahoma 73117
Univ of Pennsylvania / Division of Infectious Disease Philadelphia Pennsylvania 19104
Univ of Texas Med Branch Galveston Texas 775550835
Infectious Diseases Association of Houston Houston Texas 77030

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002162, 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 7, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002162 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →