Clinical Trials Directory

Trials / Completed

CompletedNCT02712489

A Roll-over Observational Study for the Extended Follow-up of the Volunteers of the ISS T-003 Trial

A Roll-over Observational Study for the Extended Follow-up of the Volunteers of the ISS T-003 Trial (ISS T-003 EF-UP)

Status
Completed
Phase
Study type
Observational
Enrollment
179 (actual)
Sponsor
Barbara Ensoli, MD, PhD · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

A roll-over observational study (ISS T-003 EF-UP) is being conducted to extend the follow-up of the volunteers of the ISS T-003 trial 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.

Detailed description

An open label, non-interventional study roll-over study (ISS T-003 EF-UP) is being conducted to follow-up the persistence of vaccine humoral responses as well as of the immunological and virological effects induced by the therapeutic immunization with Tat.To this aim volunteers of the ISS T-003 study are included in one year study, with visits at weeks 0 and 24 and 54. To assess the anti-Tat humoral immune response by the determination and titration of IgM, IgG and IgA anti-Tat antibodies (primary endpoint) and to evaluate CD4+ T cell counts and HIV-1 plasma viraemia (as secondary endpoint). In addition, depending on the availability of residual specimens (PBMC, serum and plasma), further laboratory tests (i.e. HIV DNA copies in blood) to investigate in-depth the immunological and virological profile of the volunteers is being performed. Physical examination is being performed to monitor the clinical status of the volunteers and to record the appearance of clinical signs and symptoms of disease progression as well as AIDS-defining events, data or records related to ARV treatment compliance. Pregnancy onset for female participants will also be recorded.

Conditions

Interventions

TypeNameDescription
OTHERNo intervention

Timeline

Start date
2015-01-01
Primary completion
2016-04-01
Completion
2016-10-01
First posted
2016-03-18
Last updated
2016-12-29

Locations

1 site across 1 country: South Africa

Source: ClinicalTrials.gov record NCT02712489. Inclusion in this directory is not an endorsement.