Study of Switching to Aflibercept 8 mg in Patients With Refractory or Dependent Exudative Age-related Macular Degeneration

Recruiting Observational Study
Exudative Age-Related Macular Degeneration
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
100 (estimated)
Sponsor
Nantes University Hospital · Other
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About This Trial
Age-related macular degeneration is a leading cause of visual impairment in older adults. In its exudative form, repeated intravitreal injections of anti-VEGF agents are required to control disease activity. A new formulation of aflibercept at a higher dose (8 mg) has been developed with the aim of extending the interval between injections. This multicenter retrospective real-world observational …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adults (≥18 years) with exudative (neovascular) age-related macular degeneration * Treated with intravitreal anti-VEGF therapy for more than 1 year * Switched to aflibercept 8 mg before July 31, 2025 * Injection interval strictly less than 12 weeks prior to switch Exclusion C…
Contacts

Jean Baptiste DUCLOYER, MD, PhD

02 40 08 34 01

jeanbaptiste.ducloyer@chu-nantes.fr

CONTACT

Alexandra Poinas, PhD

+33 2 53 48 28 57

alexandra.poinas@chu-nantes.fr

CONTACT