Evaluating intermittent triple therapies for HIV

Evaluation of Intermittent Triple Therapies in Real Life

University Hospital, Strasbourg, France · NCT06578702

This study is testing how well intermittent triple therapy works and how safe it is for adults living with HIV at the University Hospital in Strasbourg.

Quick facts

Study typeObservational
Enrollment200 (estimated)
Ages18 Years and up
SexAll
SponsorUniversity Hospital, Strasbourg, France (other)
Locations1 site (Strasbourg)
Trial IDNCT06578702 on ClinicalTrials.gov

What this trial studies

This observational study aims to assess the effectiveness and safety of intermittent triple therapy in adults living with HIV who are monitored at the University Hospital in Strasbourg. Following the validation of this treatment strategy in France through the QUATUOR trial, the study seeks to gather real-life data on its efficacy and tolerance. Participants will include those who have received intermittent treatment between January 2017 and January 2024, contributing to a better understanding of this therapeutic approach.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 and older living with HIV who have received intermittent triple therapy at the Trait d'Union/Infectious Diseases department in Strasbourg.

Not a fit: Patients who have not undergone intermittent triple therapy or those who oppose the reuse of their data for research purposes may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could provide valuable insights into a potentially effective treatment strategy for managing HIV.

How similar studies have performed: While the intermittent triple therapy approach has shown promise in previous trials in France, this study aims to provide real-world data, making it a novel contribution to the field.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion criteria:

* Adult subject (≥ 18 years old)
* Living with HIV monitored at the Trait d'Union/Infectious Diseases department in Strasbourg
* Having benefited from intermittent triple therapy between 01/01/2017 and 31/01/2024

Exclusion criteria:

* Subject (and/or their legal representative if applicable) having expressed their opposition to the reuse of their data for scientific research purposes.

Where this trial is running

Strasbourg

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: HIV Infections, Intermittent Triple Therapy

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.