Disease · MONDO_0005417
wet macular degeneration
6 sourcesdiseases-2026-09-18-0.1.0
Cite this record
ConductScience Library. wet macular degeneration. Diseases, record MONDO_0005417. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0005417
On this page
Disease
Names and IDs as Open Targets gives them. Its IDs in MeSH, Orphanet, the Disease Ontology and the NCI Thesaurus are those Open Targets states for it.
- Other names
Kuhnt-Junius degeneration, choroidal neovascularization, exudative senile macular degeneration of retina, neovascular age-related macular degeneration, wet AMD, wet ARMD, wet age related macular degeneration, wet senile macular retinal degeneration
- Open Targets
- Highest stage of its drugs
- Approval, for 8 of its 55 drugs, from DailyMed, EMA Human Drugs, FDA and TTD
- Open Targets
Drugs55
The drugs Open Targets' clinical reports study for the disease, the highest stage first, then the most trial reports. The stage is Open Targets', the highest any of its sources reports for the pair, and each row names the sources that report it.
| Drug | ChEMBL ID | Type | Open Targets' stage | Stage reported by | Reports | Of them trials | Trials shown here | Source |
|---|---|---|---|---|---|---|---|---|
| AFLIBERCEPT | CHEMBL1742982 | Protein | Approval | DailyMed and EMA Human Drugs | 70 | 55 | 55 | Drugs and targets |
| RANIBIZUMAB | CHEMBL1201825 | Antibody | Approval | DailyMed and EMA Human Drugs | 46 | 35 | 32 | Drugs and targets |
| FARICIMAB | CHEMBL4297750 | Antibody | Approval | EMA Human Drugs, FDA and TTD | 18 | 14 | 14 | Drugs and targets |
| BEVACIZUMAB | CHEMBL1201583 | Antibody | Approval | EMA Human Drugs | 13 | 11 | 8 | Drugs and targets |
| BROLUCIZUMAB | CHEMBL3707357 | Antibody | Approval | EMA Human Drugs and TTD | 13 | 11 | 11 | Drugs and targets |
| PEGAPTANIB SODIUM | CHEMBL1201421 | Small molecule | Approval | DailyMed and TTD | 7 | 4 | 4 | Drugs and targets |
| PEGPLERANIB SODIUM | CHEMBL3301576 | Approval | TTD | 4 | 2 | 0 | Drugs and targets | |
| VERTEPORFIN | CHEMBL5314346 | Small molecule | Approval | DailyMed | 4 | 2 | 2 | Drugs and targets |
| ABICIPAR PEGOL | CHEMBL4297684 | Protein | Phase 3 | ClinicalTrials.gov | 4 | 3 | 3 | Drugs and targets |
| ALTEPLASE | CHEMBL1201593 | Enzyme | Phase 3 | ClinicalTrials.gov | 1 | 1 | 1 | Drugs and targets |
1 to 10 of 55
See all 55 drugsTargets52
The targets ChEMBL's mechanism records give for the disease's drugs, through Open Targets, the most drugs first. A mechanism record says what a drug acts on, not that the target causes the disease.
| Target | Protein | Its drugs that act on it | Mechanisms | Highest stage of those drugs | Gene in Genes | Source |
|---|---|---|---|---|---|---|
| VEGFA | VEGF-A mRNA | 10 | VEGF-A mRNA RNAi inhibitor; Vascular endothelial growth factor A antagonist; Vascular endothelial growth factor A inhibitor | Approval | https://conductscience.org/library/genes/7422 | Drugs and targets |
| FLT1 | VEGFR1 mRNA | 4 | VEGFR1 mRNA rnai inhibitor; Vascular endothelial growth factor receptor inhibitor | Phase 3 | https://conductscience.org/library/genes/2321 | Drugs and targets |
| KDR | Vascular endothelial growth factor receptor | 4 | Vascular endothelial growth factor receptor 2 inhibitor; Vascular endothelial growth factor receptor inhibitor | Phase 3 | https://conductscience.org/library/genes/3791 | Drugs and targets |
| FLT4 | Vascular endothelial growth factor receptor | 3 | Vascular endothelial growth factor receptor inhibitor | Phase 3 | https://conductscience.org/library/genes/2324 | Drugs and targets |
| PDGFRB | Platelet-derived growth factor receptor | 3 | Platelet-derived growth factor receptor beta inhibitor; Platelet-derived growth factor receptor inhibitor | Phase 2 | https://conductscience.org/library/genes/5159 | Drugs and targets |
| KIT | Mast/stem cell growth factor receptor Kit | 2 | Stem cell growth factor receptor inhibitor | Phase 2 | https://conductscience.org/library/genes/3815 | Drugs and targets |
| NR3C1 | Glucocorticoid receptor | 2 | Glucocorticoid receptor agonist | Phase 2 | https://conductscience.org/library/genes/2908 | Drugs and targets |
| PDGFRA | Platelet-derived growth factor receptor | 2 | Platelet-derived growth factor receptor inhibitor | Phase 2 | https://conductscience.org/library/genes/5156 | Drugs and targets |
| PGF | Placenta growth factor | 2 | Placenta growth factor inhibitor | Approval | https://conductscience.org/library/genes/5228 | Drugs and targets |
| TLR3 | Toll-like receptor 3 | 2 | Toll-like receptor 3 activator | Phase 2 | https://conductscience.org/library/genes/7098 | Drugs and targets |
1 to 10 of 52
See all 52 targetsTrials134
Trials an Open Targets clinical report links to the disease, posted results first, then the largest. A trial is shown when the release's checks confirm its link to the disease and Drugs and targets shows its link to one of the disease's drugs. 6 more are not shown, since the checks do not confirm them.
| Trial | Title | Phase | Participants | Results first posted | Conditions | Drugs | Linked by | Source |
|---|---|---|---|---|---|---|---|---|
| NCT01245387 | Observational Study Of The Long-Term Effect Of Macugen In Patients With Wet Age-Related Macular Degeneration | 1,001 | 2011-01-07 | Macular Degeneration, Age-related Macular Degeneration, Neovascular Macular Degeneration | PEGAPTANIB SODIUM | Its record names the disease | ClinicalTrials.gov | |
| NCT02462928 | A Safety and Efficacy Study of Abicipar Pegol in Participants With Neovascular Age-related Macular Degeneration | Phase 3 | 939 | 2020-07-28 | Macular Degeneration | ABICIPAR PEGOL | Its record names the disease | ClinicalTrials.gov |
| NCT04005352 | Study to Assess the Efficacy and Safety of Brolucizumab 6mg Compared to Aflibercept 2 mg in a Treat-to-control Regimen (TALON) | Phase 3 | 734 | 2024-01-30 | Age-related Macular Degeneration | BROLUCIZUMAB | Its record names the disease | ClinicalTrials.gov |
| NCT03823287 | A Study to Evaluate the Efficacy and Safety of Faricimab in Participants With Neovascular Age-Related Macular Degeneration (TENAYA) | Phase 3 | 671 | 2022-05-04 | Wet Macular Degeneration | AFLIBERCEPT, FARICIMAB | Its record names the disease | ClinicalTrials.gov |
| NCT03823300 | A Study to Evaluate the Efficacy and Safety of Faricimab in Participants With Neovascular Age-Related Macular Degeneration (LUCERNE) | Phase 3 | 658 | 2022-05-04 | Wet Macular Degeneration | AFLIBERCEPT, FARICIMAB | Its record names the disease | ClinicalTrials.gov |
| NCT01948830 | Randomized Study for Efficacy and Safety of Ranibizumab 0.5mg in Treat-extend and Monthly Regimens in Patients With nAMD | Phase 3 | 650 | 2016-12-15 | Age-related Macular Degeneration, Choroidal Neovascularization | RANIBIZUMAB | Its record names the disease | ClinicalTrials.gov |
| NCT03805100 | Comparing the Efficacy and Safety of Biosimilar Candidate Xlucane Versus Lucentis® in Patients With nAMD | Phase 3 | 582 | 2023-11-13 | Macular Degeneration | RANIBIZUMAB | Its record names the disease | ClinicalTrials.gov |
| NCT03710564 | Study of Safety and Efficacy of Brolucizumab 6 mg Dosed Every 4 Weeks Compared to Aflibercept 2 mg Dosed Every 4 Weeks in Patients With Retinal Fluid Despite Frequent Anti-VEGF Injections | Phase 3 | 535 | 2022-07-22 | Age-Related Macular Degeneration | AFLIBERCEPT, BROLUCIZUMAB | Its record names the disease | ClinicalTrials.gov |
| NCT00460408 | Ocular Safety Of Patients Receiving Macugen For Neovascular Age Related Macular Degeneration | 501 | 2012-12-11 | Macular Degeneration | PEGAPTANIB SODIUM | Its record names the disease | ClinicalTrials.gov | |
| NCT01006538 | Macular EpiRetinal Brachytherapy Versus Lucentis® Only Treatment (MERLOT) | Phase 4 | 363 | 2019-07-22 | Macular Degeneration | BEVACIZUMAB, RANIBIZUMAB | Its record names the disease | ClinicalTrials.gov |
1 to 10 of 134
See all 134 trialsComparisons in its trials30
Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.
| Comparison | Group 1, with the outcome | Group 2, with the outcome | Participants | Trial | Source |
|---|---|---|---|---|---|
| Brolucizumab 6 mg vs Aflibercept 2 mg: Number of Participants With Treatment Emergent Non-ocular Adverse Events (Greater Than or Equal to 2% in Any Treatment Arm) - Summary Table | 182 of 366 | 185 of 368 | 734 | NCT04005352 | Trial comparisons |
| Arm A: Faricimab vs Arm B: Aflibercept: deaths from any cause | 13 of 333 | 7 of 336 | 669 | NCT03823287 | Trial comparisons |
| Arm A: Faricimab vs Arm B: Aflibercept: serious adverse events | 80 of 333 | 93 of 336 | 669 | NCT03823287 | Trial comparisons |
| Arm A: Faricimab vs Arm B: Aflibercept: deaths from any cause | 10 of 331 | 14 of 326 | 657 | NCT03823300 | Trial comparisons |
| Arm A: Faricimab vs Arm B: Aflibercept: serious adverse events | 91 of 331 | 101 of 326 | 657 | NCT03823300 | Trial comparisons |
| Group I Ranibizumab 0.5 mg TER vs Group II Ranibizumab 0.5 mg Monthly: serious adverse events | 39 of 323 | 42 of 326 | 649 | NCT01948830 | Trial comparisons |
| Xlucane (Proposed Ranibizumab Biosimilar) vs Lucentis (Ranibizumab): deaths from any cause | 8 of 292 | 3 of 290 | 582 | NCT03805100 | Trial comparisons |
| Xlucane (Proposed Ranibizumab Biosimilar) vs Lucentis (Ranibizumab): serious adverse events | 33 of 292 | 35 of 290 | 582 | NCT03805100 | Trial comparisons |
| Arm A: Epimacular Bracytherapy + Lucentis® vs Arm B: Lucentis® Only: Percentage of Subjects Gaining ≥ 15 ETDRS Letters | 3 of 244 | 6 of 119 | 363 | NCT01006538 | Trial comparisons |
| Arm A: Epimacular Bracytherapy + Lucentis® vs Arm B: Lucentis® Only: Percentage of Subjects Gaining ≥ 0 ETDRS Letters | 91 of 244 | 55 of 119 | 363 | NCT01006538 | Trial comparisons |
1 to 10 of 30
See all 30 comparisons in its trialsPapers from its trials133
The papers the trials shown here list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.
Data dates
The date of each source this release read.
Sources 6
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- NLM's MeSHNLM's terms
- Open TargetsCC0 1.0
- PubMedNLM's terms
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- NLM's MeSHNLM's
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this disease from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/diseases/v1/MONDO_0005417
GET https://conductscience.org/api/diseases/v1/MONDO_0005417/drugs?page=2