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Recruiting NCT05215704

NCT05215704 Ex Vivo Characterization and Targeting of the Latent HIV Infected Reservoir to Cure HIV

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Clinical Trial Summary
NCT ID NCT05215704
Status Recruiting
Phase
Sponsor Erasmus Medical Center
Condition HIV Infections
Study Type OBSERVATIONAL
Enrollment 40 participants
Start Date 2012-01-01
Primary Completion 2030-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 40 participants in total. It began in 2012-01-01 with a primary completion date of 2030-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Combination antiretroviral therapy (cART) blocks intracellular human immunodeficiency virus (HIV) replication in CD4+ T-lymphocytes, but fails to eliminate latent HIV infected CD4+ T-lymphocytes. About 7 (range \<1-100) in 106 of these cells are latently infected and can cause reactivation of proviral HIV when cART is stopped. These latently infected cells form the reservoir and must be targeted in order to cure HIV. We would like to further investigate this reservoir and assess potential interventions to eradicate it. One promising option is to further study the influence of HIV latency disruptors (latency reversing agents, LRA) on the HIV infected reservoir. These agents are used in shock and kill strategies that disrupt latency by LRA followed by the selective (induced) killing of the reservoir cell due to viro-pathogenic effects. For accurate assessment of the reservoir and potential cure strategies, including the impact of LRA on the reservoir, a large reservoir and sufficient cells for analysis are desirable. Our understanding on the reservoir comes from in vitro lymphocyte models and early ex vivo studies. Additional studies of patients with different clinical phenotypes including untreated versus treated versus the rare individuals that control HIV spontaneously are increasingly relevant to the field. Especially this last category represent biological examples of viral control without cART and are useful to study the factors that set them apart from those that need treatment for their HIV. This study aims to deepen our understanding of the HIV reservoir and cure strategies, foremost, shock and kill strategies. We will do this by setting up a durable ex vivo platform for HIV reservoir and cure studies of which the samples can be used for hypothesis generation for in-vivo studies. A project from the Erasmus MC HIV Eradication Group (EHEG).

Eligibility Criteria

Inclusion Criteria: 1. Age 18 years or older. 2. Confirmed HIV-1 or HIV-2 infection. Exclusion Criteria: 1. Inability to place 2.5 cm venous catheter or perform phlebotomy 2. Major comorbidities: A. Severe symptomatic anemia B. Recent symptomatic cardiovascular event (unstable angina pectoris, decompensated heart failure, myocardial infarction). 3. The inability to participate due to any other relevant medical, social, environmental, psychological, factors or according to the HIV treating physician's judgement

Contact & Investigator

Central Contact

Casper Rokx, MD PhD

✉ c.rokx@erasmusmc.nl
Principal Investigator

Casper Rokx, MD PhD

PRINCIPAL INVESTIGATOR

Erasmus Medical Center

Frequently Asked Questions

Who can join the NCT05215704 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying HIV Infections. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05215704 currently recruiting?

Yes, NCT05215704 is actively recruiting participants. Contact the research team at c.rokx@erasmusmc.nl for enrollment information.

Where is the NCT05215704 trial being conducted?

This trial is being conducted at Rotterdam, Netherlands.

Who is sponsoring the NCT05215704 clinical trial?

NCT05215704 is sponsored by Erasmus Medical Center. The principal investigator is Casper Rokx, MD PhD at Erasmus Medical Center. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology