Active clinical trials
Dry / Atrophic AMD
Dry AMD is a chronic, progressive disease that can affect both eyes or asymmetrically. It causes blurred vision or reduced central vision.
Study for the Treatment of Geographic Atrophy Secondary to Dry AMD
- Phase : 3
- Duration: 2 and a half years
- Impact: International
- Treatment: Human immunoglobulin monoclonal antibody
- Cost to the patient: € 0
- Travel expenses: Covered
Recruitment open
Study for the treatment of GEOGRAPHIC ATROPHY associated with DRY AMD
- Phase: 2
- Duration: 18 months
- Impact: International
- Treatment: Intravitreal solution of avacincaptad pegol
- Cost to the patient: € 0
- Travel expenses: Covered
Recruitment open
Study for the treatment of Geographic Atrophy associated with dry AMD
- Phase 2
- Duration: 5 years (from the 1st year onwards, biannual follow-ups)
- Impact: International
- Treatment: single intravitreal dose
- Cost for the patient: €0
- Travel expenses: Covered
Planned activation: July 2026
Diabetic macular oedema
This is a condition that occurs in diabetic patients due to the accumulation of fluid in the retina.
Study for the treatment of Diabetic Macular Oedema (DMO)
- Phase 3
- Duration: 2 years
- Impact: International
- Treatment: Intravitreal
- Cost to the patient: 0 €
- Travel expenses: Covered
Planned activation: July 2026
Dry Eye
Study on the treatment of Moderate and Severe Dry Eye
- Duration: 3 months
- Impact: National
- Treatment: Oral treament
- Cost for the patient: €0
Planned activation: July 2026
Neurotrophic keratopathy
Clinical Trial in Patients with Persistent Corneal Epithelial Defect (PCED)
Treatments for these patients are often limited to lubrication and protection, as there are no approved treatments available for PCED, and in many cases, patients do not respond to standard therapy.
Study for the treatment of moderate to severe PCED due to neurotrophic keratopathy
Phase: 2/3
- Duration: 56 to 84 days
- Impact: International
- Treatment: Ophthalmic gel
- Cost to patient: €0
- Travel expenses: Covered
Open recruitment
Intracorneal Rings
Prospective study to assess the clinical outcome of the Intrastromal Corneal Ring implanted in patients with Keratoconus.
- Duration: 3 years
- Impact: International
- Treatment: Corneal ring implanted using femtosecond laser
- Cost of lenses for the patient: €0
- Travel expenses: Covered
Open recruitment
Intraocular Lenses
Post-market clinical follow-up (PMCF) study with a presbyopia-correcting intraocular lens in adults over 55 years of age.
- Duration: 3 years
- Impact: International
- Treatment: Implantation of a presbyopia-correcting intraocular lens for patients with cataracts
- Cost of lenses for the patient: €0
- Travel expenses: Covered
Recruitment closed
Wet / Neovascular AMD
Clinical trial for the treatment of WET Age-Related Macular Degeneration (AMD)
Phase: 3 – B
- Duration: 18 months
- Impact: International
- Treatment: Gene therapy with recombinant viral vector. Administration via the subretinal route.
- Cost to the patient: €0
- Travel expenses: Covered
Recruitment open
Study for the treatment of POLYPOIDAL CHOROIDAL VASCULOPATHY (PCV)
Phase: 4
- Duration: 2 years
- Impact: International
- Treatment: Intravitreal solution of faricimab
- Cost to the patient: €0
- Travel expenses: Covered
Recruitment open
Pivotal study for the treatment of wet AMD
Phase 2/3
- Duration: 24 months
- Impact: International
- Treatment: Intravitreal
- Cost for the patient: €0
- Travel expenses: Covered
Planned activation: June 2026
Trial for the treatment of wet Age-related Macular Degeneration (AMD)
Phase: 3
- Duration: 12 months
- Impact: International
- Tratamiento: Intravítreo
- Cost for the patient: €0
- Travel expenses: Covered
Planned activation: September 2026
Study for patients with subretinal hyperreflective material associated with neovascular membranes
Phase 4
- Duration: 30 months
- Impact: Nacional
- Treatment: Intravitreal
- Cost for the patient: €0
Planned activation: July 2026
Application form
Please complete the form and select the clinical study that interests you the most. After receiving your application, we will contact you to start the participation process.