Recruiting

Observational Study

Sponsor:

UCLA

Code:

NCT00187512

Conditions

HIV Infections

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

SCOPE is an observational, prospective study of HIV-1 infected volunteers designed to provide a specimen bank of samples with carefully characterized clinical data. SCOPE specimens will be used to examine multiple questions involving virologic, immunologic, and host factors involved in HIV-1 infection, progression, non-progression, response to treatment, control of HIV-1 virus, and evolution of drug resistance.

Conditions

HIV Infections

Study ID

NCT00187512

Start date

Mar, 2000

Status verified date

Sep, 2026

Completion date

Dec, 2033

Anticipated

Primary completion date

Dec, 2032

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

SCOPE is currently recruiting HIV-1 infected subjects with any of the following criteria:

1. Documented HIV viral load less than 2000 copies/ml WITHOUT taking antiretroviral therapy
2. Undetectable HIV viral load with CD4 T-cells consistently less than 350 for the last 12 months while taking a stable antiretroviral regimen.
3. Antiretroviral naive and planning to start an antiretroviral regimen - any CD4 or HIV viral load acceptable.
4. Long-term Non Progressors: HIV-positive at least 10 years, no antiretroviral therapy for the past 10 years or more, any viral load acceptable, CD4-T cell count always above 500.

Exclusion Criteria:

1. Active opportunistic infection or systemic treatment for opportunistic infection within the last 4 months (oral candidiasis acceptable)
2. Active treatment for cancer
3. Active treatment for hepatitis C requiring interferon based therapy
4. Immunosuppressive therapy taken within the last 4 months

Study Design

Enrollment

2500 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • The general theme of this core is to investigate the relationship between the virologic response to antiretroviral therapy and clinical outcome. [ Time Frame: Ongoing ]

Central Contacts and Locations

Central contacts

Locations

San Francisco General Hospital

Recruiting

San Francisco, California, United States, 94110

Contacts

Principal Investigator:

Steven G. Deeks, M.D.

More Information

Sponsor

University of California, San Francisco

Last update posted

Sep 8, 2026

Last verified

Sep, 2026

Keywords

  • HIV
  • Antiretroviral Agents
  • Drug Resistance, Multiple
  • Long Term Non Progression
  • Long Term Non Progressor
  • Elite Suppression
  • Elite Suppressor
  • Natural History
  • Observational

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of California, San Francisco on 2026-09-08.