Eye scan showdown: faricimab vs ranibizumab in diabetic retinopathy
NCT ID NCT07520045
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two eye injections—faricimab and a biosimilar version of ranibizumab—in 100 adults with diabetic retinopathy. Researchers will use eye scans (OCT and OCT angiography) to see which drug leads to better early changes in the retina after three monthly doses. The goal is to find imaging markers that predict who responds best to each treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- faricimab and biosimilar ranibizumab (eye injections)
- What this could lead to
- If successful, this study could help doctors choose the best eye injection for each patient with diabetic retinopathy based on early imaging signs.
- What could go wrong
- This is a small, early-stage study (100 people) that only looks at imaging changes after three doses. It does not test long-term vision outcomes or safety, so results may not change practice directly.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Jun 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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18 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: * Adults aged ≥18 years * Diabetic retinopathy with or without central macular edema * Indication for intravitreal anti-VEGF therapy according to current clinical guidelines * Ability to provide written informed consent Exclusion Criteria: * Intravitreal anti-VEGF or corticosteroid treatment in the study eye within 5 months prior to enrollment * Any intraocular surgery (including cataract surgery) 3 months prior intraocular surgery to enrollment * Retinal laser photocoagulation in the study eye within 3 months prior to enrollment * Presence of other ocular, retinal or macular diseases that may affect OCT/OCTA findings or visual acuity (e.g., age-related macular degeneration, retinal vascular occlusions) * Retinal detachment, preretinal fibrosis, vitreomacular traction * Significant media opacities (e.g., dense cataract, vitreous hemorrhage) precluding reliable OCT/OCTA imaging * Uncontrolled glaucoma (intraocular pressure \> 30 mmHg in study eye) * Active ocular inflammation * Suspected active ocular infection in either eye * Any febrile illness within 1 week prior to first injection * History or presence of any clinically significant disease, non-diabetic metabolic disorder, abnormal physical examination finding, or laboratory abnormality that, in the opinion of the investigator, may contraindicate treatment with faricimab or biosimilar ranibizumab, interfere with the interpretation of study results, or place the participant at increased risk of treatment-related complications. * Women who are pregnant, breastfeeding, or planning pregnancy within the next 100 weeks * Known hypersensitivity to faricimab or biosimilar ranibizumab or any of its excipients * Participation in another clinical trial that may affect study outcomes * Inability to comply with study procedures or follow-up
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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
1 site. 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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University Hospital Osijek
RECRUITINGOsijek, 31000, Croatia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- High-Dose eye injection tested against stubborn diabetic swelling
- One eye injection, four targets: GenSci148 tested against retinal swelling
- Can one shot in the eye treat diabetic macular edema?
- Could a pill replace eye injections for diabetic vision loss?
- Can a One-Time gene therapy offer lasting protection for diabetic retinopathy?
- Can a new eye injection beat the current standard for diabetic vision loss?