Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
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RecruitingNot a traditional drug phaseobservationalRules rewrite

Not a traditional drug phase: testing Lenacapavir Injection for HIV I Infection

For most people with HIV (PWH), an effective antiretroviral regimen can be devised. However, some PWH have multiple treatment failures due to viral resistance or unacceptable side effects to medication and no longer have durable viral suppression.

Official registry: https://clinicaltrials.gov/study/NCT06799338 · Centre de Recherches et d'Etude sur la Pathologie Tropicale et le Sida · enrollment listed as 80

What this phase means

This is an observational study. You are not assigned a new experimental drug. Researchers measure what already happens in your care or in daily life.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

This listing is observational (StudyType). The registry does not assign a new experimental drug as the study intervention.

They plan to enroll about 80 people at Paris. Taking part typically means taking a study drug (or dummy pill) plus check-ins.

Official title (unrewritten)

Real World Use of Lenacapavir, as an add-on to an Optimized Background Regimen in France: a Retrospective Observational Study (LENAddOn)

Interventions: Lenacapavir Injection

Primary outcome (registry wording): Measure the number of participants who received lenecapavir injection

Who it is for (from inclusion criteria)

  • Ages 18 Years to any
  • Adults (≥18 years);
  • With HIV-1 infection;
  • Who received a first dose of LEN (oral or injectable) with and OBR from the ending of the French national early access program (20 June 2023) to 30 June 2024;
  • Who did not refuse the collection and use of their data

Public study contact (from the registry)

Yasmine DUDOIT

+33 (0)1 42 16 41 81

yasmine.dudoit@aphp.fr

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

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FAQ about this NCT record

Is NCT06799338 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT06799338?

Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT06799338?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary