drug · protein
EYLEA HD
Marketedupdated 5mo agoby $REGN REGENERON PHARMACEUTICALS, INC.🔗 ChEMBL
Approvedannual revenue · 2024–2024peak $9.4B
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🐶 often sniffed alongside
top 8- tagApproval44 co-mentions · 15 sources
- drugEylea32 co-mentions · 15 sources
- drugYESAFILI18 co-mentions · 7 sources
- drugaflibercept biosimilar17 co-mentions · 10 sources
- drugOPUVIZ8 co-mentions · 4 sources
- drugENZEEVU6 co-mentions · 3 sources
- companySamsung Bioepis Co Ltd4 co-mentions · 4 sources
- companyBiocon Biologics Ltd4 co-mentions · 2 sources
Protein drug with a maximum clinical stage of Approval (across all indications), with 16 approved and 39 investigational indications.
indications
investigational
Diabetic Macular Edema
targets
Placenta growth factorVascular endothelial growth factor A, long form
all catalysts(5)
approval · 5
Aug 18, 2023
approval
$REGN757.53-3.87%
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
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Dec 14, 2023
approval
$REGN757.53-3.87%
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
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Oct 10, 2024
approval
$REGN757.53-3.87%
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
→
Nov 19, 2025
approval
$REGN757.53-3.87%
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
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Apr 2, 2026
approval
$REGN757.53-3.87%
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
→
Trials studying EYLEA HD
- —An Observational Study to Collect Data on How Aflibercept (Eylea) Given Using a Paediatric Dosing Device is Used in Preterm Babies With Retinopathy of Prematurity in the United Kingdom (UK)
- phase3A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-002)
- phase2A Study to Test Whether BI 764524 Helps People With an Eye Condition Called Diabetic Retinopathy
- phase2Study of AR-14034 in Participants With Neovascular Age-Related Macular Degeneration (nAMD)
- phase3A Study to Evaluate the Efficacy and Safety of Tabirafusp Tedromer Compared to Aflibercept in Participants With DME - ALTO
- phase3A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degeneration
- phase3Efficacy and Safety of LX102 Gene Therapy in Patients With Neovascular Age-related Macular Degeneration (nAMD) (STELLAR)
- phase3A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUCIA) Primary Efficacy Will be Determined at Week 56
News(10)
- Kodiak skyrockets on positive study data for 2 eye drugsThe Phase 3 findings suggested Kodiak might have multiple threats to Regeneron’s Eylea and added more than $3 billion to the company’s market value.biopharma_dive · 4h ago
- Kodiak's stock soars as it clinches crucial Phase 3 win for Eylea competitorKodiak Sciences appears to have an Eylea successor on its hands. The Silicon Valley biotech said its experimental drug Zenkuda performed as well as Eylea in a progressive eye disease known as wet a…endpoints · 5h ago
- Kodiak Sciences’ stock soars 166% after 2 assets match Eylea in Phase 3 trialKodiak Sciences will head to regulators with one of the candidates, an anti-VEGF antibody called zenkuda, after the late-stage results.biospace · 5h ago
- STAT+: AbbVie wins FDA nod for Parkinson’s pillThe FDA has approved AbbVie’s once-daily Parkinson’s pill for sales, based on a late-stage study that showed the drug helped improve symptoms.stat · 6h ago
- Kodiak's stock doubles as resurrected eye disease drug matches Eylea in phase 3Two of Kodiak Sciences’ drug candidates have matched aflibercept in a phase 3 clinical trial, positioning the biotech to seek FDA approval of one of the eye disease assets this year.fiercebiotech · 12h ago
- Merck sees pivotal victory for $3B eye disease prospectMerck & Co.’s Brunello trial has hit its primary endpoint, shedding light on the effects of a trispecific diabetic macular edema (DME) drug candidate that the Big Pharma bought in a $3 billion take…fiercebiotech · 4d ago
- Regeneron to challenge Ipsen as FDA clears bone disease drugPasatru’s approval sets up a market battle in a rare indication where the only available treatment has generated disappointing sales.biopharma_dive · 1mo ago
- EyePoint’s bid to compete with Eylea falls flatEyePoint’s experimental eye treatment came up short of Eylea, the current go-to option for wet age-related macular degeneration, according to results of a Phase 3 trial. The company’s shares {$EYPT…endpoints · 1mo ago
- EyePoint plummets on pivotal data for main drugThough its drug missed the key goal of a wet AMD study, EyePoint — as well as analysts — see a path toward approval. Investors may be harder to win over, however.biopharma_dive · 1mo ago
- EyePoint’s Phase 3 fail sends stock spiraling amid next-gen AMD raceEyePoint’s quest to reduce treatment burden for patients with age-related macular degeneration has hit a bump in the road, with a clinical miss driving the biotech’s stock down by 70%.biospace · 1mo ago
Data sources
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