Remigromig clinical trials
Remigromig is named as an intervention in 3 current clinical trials in our USA, UK, Germany, France, Spain, Italy, Poland, Austria, Czechia, Portugal, Turkey, Australia, Israel, Brazil, Mexico and Japan registers. 1 is recruiting patients now. The most common phase is Phase 2/3. The lead sponsor is EyeBiotech Ltd. The most-studied condition is Diabetic Macular Edema (DME).
Patient leaflets for Remigromig
The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.
- UKUnited Kingdom: Search MHRA ProductsPatient information leaflets and SmPCs for UK-licensed products.
- USUnited States: Search DailyMedFDA-approved labels, including patient and medication guides.
Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.
Trials by status
Trials by phase
Clinical trials of Remigromig
3 trials| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
A Dose-masked Study of Intravitreal Remigromig (EYE103) in Participants With NVAMD or Macular Edema Following BRVO
NCT07205887 · Neovascular Age-Related Macular Degeneration (NVAMD), Branch Retinal Vein Occlusion (BRVO)
|
Phase 2 | Recruiting | EyeBiotech Ltd | USA |
|
A Study to Evaluate the Efficacy and Safety of 2 Doses of Remigromig (EYE103) Compared With Ranibizumab (0.5 mg) in Participants With DME
NCT06571045 · Diabetic Macular Edema (DME)
|
Phase 2/3 | Active, closed | EyeBiotech Ltd | UK, USA, Germany, France, Spain, Italy, Poland, Austria, Czechia, Portugal, Turkey, Australia, Israel |
|
A Study of 2 Doses of Remigromig (EYE103) Compared With Ranibizumab (0.5 mg) in Participants With DME
NCT06957080 · Diabetic Macular Edema (DME)
|
Phase 2/3 | Active, closed | EyeBiotech Ltd | USA, Brazil, Mexico, Japan |
Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.
Conditions studied with Remigromig
3 conditionsSponsors
lead sponsor per trial| Lead sponsor | Trials |
|---|---|
| EyeBiotech Ltd | 3 |
By country register
A trial with sites in more than one country appears in each of those registers.
Related compounds
Questions about Remigromig trials
How many clinical trials are testing Remigromig?
3 current trials in our USA, UK, Germany, France, Spain, Italy, Poland, Austria, Czechia, Portugal, Turkey, Australia, Israel, Brazil, Mexico and Japan registers name Remigromig (also registered as EYE103) as a drug or biological intervention, as of the registry sync on 22 October 2026. Completed and withdrawn studies are not counted.
Are Remigromig trials recruiting patients?
Yes. 1 of the 3 trials is recruiting: 1 with sites in USA. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Who sponsors Remigromig clinical trials?
The lead sponsor is EyeBiotech Ltd. The number in brackets is how many trials each organisation leads.
Where does this information come from?
Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Remigromig works or whether it is effective, and it is not medical advice.
How this page is built
Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Remigromig works or whether it is effective. Each trial links to its own record so you can check it yourself.
- ClinicalTrials.gov (U.S. National Library of Medicine) ↗ Trial IDs, titles, intervention names and synonyms, phase, overall status, lead sponsor and conditions for every trial on this page
This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Remigromig (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 22 Oct 2026. How every register is built: methodology · fixes we have made: corrections log.