Can blocking rogue immune cells stop a leading cause of blindness?
NCT ID NCT04697095
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
This study tests whether immune cells called monocytes from people with the atrophic form of age-related macular degeneration (AMD) survive longer on retinal cells than monocytes from healthy people. Researchers will collect blood samples from 80 participants, extract monocytes, and culture them on retinal pigment epithelial cells in the lab. The goal is to understand why these cells accumulate in the retina and whether targeting them could lead to future treatments for atrophic AMD, which currently has no therapy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Blood sample collection for monocyte extraction and laboratory analysis
- What this could lead to
- If monocytes from atrophic AMD patients survive longer on retinal cells, it could point to new therapies that block this harmful accumulation.
- What could go wrong
- This is an early laboratory study with a small sample, so findings may not translate to treatments. The research only observes cells, not living patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2022
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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15 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: General criteria: * Male or female older than 50, * Provide written informed consent, * Patient affiliated to French social security, * Maximum sampling volume (care + research) per 30-day period to be adapted according to the weight of the patient Specific criteria: Patient presenting in both eyes: * Either the same type of AMD defined according to the modified international AREDS study (Ferris et al. 2013), * or early AMD in one eye and atrophic AMD in the other eye, the patient will therefore be defined as being atrophic * or early AMD in one eye and exudative AMD in the other eye, the patient will therefore be defined as exudative, * or no retinal pathology (control group). Exclusion Criteria: General criteria: * Patient whose weight is less than 50kg, * Adult patient under guardianship or curatorship or unable to express consent, * Person deprived of liberty, * Patient participating in an ongoing clinical trial during the inclusion visit, Specific criteria: * Patient with atrophic AMD in one eye and exudative AMD in the other eye, * Patient presenting with chronic retinal pathologies other than AMD, defined according to the modified international AREDS study (Ferris et al. 2013) , in the included eye, * Patient taking systemic drugs with an immunomodulatory action: immunosuppressants, immunomodulators, chemotherapy or corticosteroids, * Patient with systemic pathologies modifying their immune status, * Patient with a history of diabetes, * Patient who had dynamic phototherapy on the included eye.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hôpital Edouard Herriot
RECRUITINGLyon, 69003, France
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Service d'ophtalmologie-HOSPICES CIVILS DE LYON - Hôpital de la Croix-Rousse
RECRUITINGLyon, 69004, France
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