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NCT05680948Completed

Extended Follow-Up of the ISS T-003 Trial Volunteers (ISS T-003 EF-UP2020)

A Roll-Over Observational Study for the Extended Follow-Up of the Volunteers of the ISS T-003 Trial (ISS T-003 EF-UP2020)

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

A further extension of the follow-up of the volunteers of the ISS T-003 trial is being conducted in order to evaluate the persistence of vaccine immunogenicity as well as of the immunological and virological effects induced by the therapeutic immunization with Tat after about 10 years from vaccination.

Status (registry)
Completed
Study type
Observational
Enrollment
179 (actual)
First submitted
5 Dec 2022
Start date
25 Jan 2023
Primary completion date
31 Dec 2023
Lead sponsor
Istituto Superiore di Sanità
Diseases
HIV
NCT number
NCT05680948

What you commit to

  • Study type: Observational
  • Participants enrolled: 179
  • From 25 Jan 2023 to the primary completion date, 31 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • The absence of any of the above criteria will exclude the participants from the study.

Who the study is looking for

  • previous participation in the ISS T-003 EF-UP study without withdrawal of consent;
  • availability to participate in the ensuing extended follow-up study;
  • signed informed consent.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mecru Clinical Research Unit (MeCRU)
Coordinator of this site? Confirm its status
MedunsaSouth AfricaUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.