Biomarkers for Post-treatment Control in HIV: International Study of the EU2Cure Research Consortium (Phase I)

NCT07692295 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-07-09

No results posted yet for this study

Summary

Antiretroviral therapy (ART) has transformed HIV from a deadly disease into a lifelong infection that can be controlled. Nevertheless, in the majority of people living with HIV (PWH), discontinuation of ART results in viral rebound due to a latent proviral reservoir. Rarely, individuals known as post-treatment controllers (PTC) demonstrate prolonged viral control even after ceasing ART. Investigating the underlying mechanisms driving this sustained viral control has been a goal for the HIV research community. However, previous studies have been hindered by the scarcity of PTC cases, thereby restricting the potential for associative and translational research. Consequently, the aim of this study is to collect and meta-analyse the data from prior trials where PTC have been identified, as well as to retrospectively identify PTC from the routine care outside trials in a multicentre, multinational study called EU2Control. The aggregated clinical data, and the already collected material from trials where PWH consented for use in additional studies on HIV, will be analyzed with the goal to identify predictive biomarkers for sustained viral control. This study will be part of the research line on HIV cure from an ongoing collaborative consortium (EU2Cure). The first phase of this research line involves a retrospective cohort for meta-analysis and establishment of a biobank.

Conditions

Interventions

OTHER

No Intervention: Observational Cohort

No intervention (observational cohort)

Sponsors & Collaborators

  • EU2Cure consortium

    collaborator UNKNOWN
  • Radboud University Medical Center

    collaborator OTHER
  • European Aids Treatment Group (EATG), Brussels, Belgium

    collaborator UNKNOWN
  • University Hospital, Ghent

    collaborator OTHER
  • University Ghent

    collaborator OTHER
  • Oslo University Hospital

    collaborator OTHER
  • Charite University, Berlin, Germany

    collaborator OTHER
  • Institut Pasteur

    collaborator INDUSTRY
  • University of Aarhus

    collaborator OTHER
  • IrsiCaixa

    collaborator OTHER
  • Fundació Lluita contra les Infeccions

    collaborator UNKNOWN
  • IRCCS San Raffaele

    collaborator OTHER
  • Imperial College London

    collaborator OTHER
  • University of Oxford

    collaborator OTHER
  • Guy's and St Thomas' NHS Foundation Trust

    collaborator OTHER
  • Chelsea and Westminster NHS Foundation Trust

    collaborator OTHER
  • Pomeranian Medical University Szczecin

    collaborator OTHER
  • Hospital Universitari Vall d'Hebron Research Institute

    collaborator OTHER
  • Medical University of Warsaw

    collaborator OTHER
  • Centre Hospitalier Universitaire Vaudois

    collaborator OTHER
  • Erasmus Medical Center

    lead OTHER

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-10-31
Primary Completion
2027-10-31
Completion
2027-12-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07692295 on ClinicalTrials.gov