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Priya Life Science Compound trial record
Compound · clinical trials

Lucentis clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 9 trials in our USA, Mexico, Germany, Spain, Austria, China, UK, France, Italy, Poland, Czechia, Portugal, Turkey, Australia, Israel, Brazil and Japan registers that name Lucentis as an intervention. Synced 9 Nov 2026
9Current trials
2Recruiting now
7Lead sponsors
17Country registers
At a glance

Lucentis is named as an intervention in 9 current clinical trials in our USA, Mexico, Germany, Spain, Austria, China, UK, France, Italy, Poland, Czechia, Portugal, Turkey, Australia, Israel, Brazil and Japan registers. 2 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is EyeBiotech Ltd (2). The most-studied condition is Diabetic Macular Edema (DME).

Patient leaflets for Lucentis

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-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

  • Recruiting222%
  • Active, closed667%
  • By invitation111%

Trials by phase

  • Phase 3444%
  • Phase 2/3333%
  • Phase 2111%
  • Phase 4111%
01

Clinical trials of Lucentis

9 trials
StudyPhaseStatusLead sponsorRegisters
Pharmacogenomics of antiVEGF in Patients With Age-Associated Macular Degeneration (AMD)
NCT06952452 · ClinicalTrials.gov ↗ · Wet Age-related Macular Degeneration
Phase 3 Recruiting Parc de Salut Mar Spain
Efficacy Evaluation Study of BAT5906 and Lucentis® in Patients With Diabetic Macular Edema
NCT07515079 · ClinicalTrials.gov ↗ · Diabetic Macular Edema (DME)
Phase 3 Recruiting Bio-Thera Solutions China
Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space for Participants With nAMD
NCT05210803 · Neovascular Age-Related Macular Degeneration (nAMD)
Phase 2 By invitation AbbVie USA, Mexico
A Study Assessing Corneal Endothelial Cells in Participants With Neovascular Age-related Macular Degeneration (nAMD) Treated With the Port Delivery System With Ranibizumab (PDS)
NCT04853251 · ClinicalTrials.gov ↗ · Neovascular Age-related Macular Degeneration
Phase 4 Active, closed Genentech, Inc USA
Combination of Ranibizumab and Targeted Laser Photocoagulation
NCT04444492 · ClinicalTrials.gov ↗ · Central Retinal Vein Occlusion With Macular Edema
Phase 3 Active, closed University of Giessen Germany, Austria
TAB014 Compared to Lucentis® in Patients with Neovascular Age-related Macular Degeneration
NCT05461339 · ClinicalTrials.gov ↗ · Neovascular Age-related Macular Degeneration
Phase 3 Active, closed BioDlink Biopharm Co., Ltd China
Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administered Via Subretinal Delivery One Time in Participants With nAMD
NCT04704921 · AMD, nAMD, Wet Age-related Macular Degeneration
Phase 2/3 Active, closed AbbVie USA, Mexico
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.

02

Conditions studied with Lucentis

8 conditions
Diabetic Macular Edema (DME)3Neovascular Age-related Macular Degeneration2Wet Age-related Macular Degeneration2Neovascular Age-Related Macular Degeneration (nAMD)1AMD1nAMD1wAMD1Central Retinal Vein Occlusion With Macular Edema1
05

Related compounds

06

Questions about Lucentis trials

How many clinical trials are testing Lucentis?

9 current trials in our USA, Mexico, Germany, Spain, Austria, China, UK, France, Italy, Poland, Czechia, Portugal, Turkey, Australia, Israel, Brazil and Japan registers name Lucentis as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are Lucentis trials recruiting patients?

Yes. 2 of the 9 trials are recruiting: 1 with sites in Spain and 1 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Lucentis clinical trials?

EyeBiotech Ltd (2), AbbVie (2), Genentech, Inc (1) and Bio-Thera Solutions (1), among 7 lead sponsors in total. 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 Lucentis works or whether it is effective, and it is not medical advice.

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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 Lucentis works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Lucentis (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 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.