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  1. pharmadog
  2. ›drugs
  3. ›EYLEA HD
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EYLEA HD

Marketedupdated 3mo ago
by $REGN REGENERON PHARMACEUTICALS, INC.🔗 ChEMBL
Approved
annual revenue · 2024–2024peak $9.4B
2024: $9.4B2024$9.4B
community read0 votes

🐶 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
$REGN826.64-1.69%
3y ago
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
→
Dec 14, 2023
approval
$REGN826.64-1.69%
3y ago
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
→
Oct 10, 2024
approval
$REGN826.64-1.69%
2y ago
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
→
Nov 19, 2025
approval
$REGN826.64-1.69%
9mo ago
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
→
Apr 2, 2026
approval
$REGN826.64-1.69%
5mo ago
EYLEA HD (AFLIBERCEPT) — FDA approval
EYLEA HD
→

Trials studying EYLEA HD

  • phase3A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degenerationrecruitingn=304
  • phase3Efficacy and Safety of LX102 Gene Therapy in Patients With Neovascular Age-related Macular Degeneration (nAMD) (STELLAR)recruitingn=388
  • phase3A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUCIA) Primary Efficacy Will be Determined at Week 56active not recruitingn=400
  • phase3CAPRI: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DMErecruitingn=240
  • phase3COMO: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DMErecruitingn=240
  • phase2A Study to Test Whether BI 764524 Helps People With an Eye Condition Called Diabetic Retinopathyactive not recruitingn=190
  • phase3A Clinical Trial of MK-8748 Compared to Aflibercept in Participants With Diabetic Macular Edema (MK-8748-005)not yet recruitingn=1,104
  • phase3A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-002)recruitingn=960
more trials →

News(10)

  • Regeneron to challenge Ipsen as FDA clears bone disease drug
    Pasatru’s approval sets up a market battle in a rare indication where the only available treatment has generated disappointing sales.
    biopharma_dive · 11h ago
  • EyePoint’s bid to compete with Eylea falls flat
    EyePoint’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 · 3d ago
  • EyePoint plummets on pivotal data for main drug
    Though 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 · 3d ago
  • EyePoint’s Phase 3 fail sends stock spiraling amid next-gen AMD race
    EyePoint’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 · 3d ago
  • Scholar Rock rejigs approval filing after FDA flags violations at Novo plant
    Despite earlier claims of improvement at the fill-finish plant, the FDA has classified the facility as Official Action Indicated based on inspection findings.
    biospace · 9d ago
  • Scholar Rock ditches Novo’s legacy Catalent plant in FDA refiling of SMA drug
    Scholar Rock has dropped Novo Nordisk’s troubled Catalent facility as a contract manufacturer in its FDA refiling for apitegromab, a spinal muscular atrophy candidate, after a recent inspection of…
    fiercebiotech · 10d ago
  • Regeneron’s ‘aversion’ to M&A questioned as bumper Q2 builds war chest
    Calls for Regeneron to step up dealmaking have intensified as the company has established an $18 billion cash pile and suffered clinical trial setbacks.
    biospace · 21d ago
  • FDA scientists question Capricor data; Legend CEO steps down
    Capricor shares lost much of their value ahead of a high-stakes advisory committee meeting. Elsewhere, Ying Huang’s resignation extended a stock slide for Legend and AstraZeneca disclosed more pipe…
    biopharma_dive · 24d ago
  • Roche drops TCE for lupus, but hasn’t given up on autoimmune cell therapies
    Roche may have scrapped work on a T-cell engager being evaluated for lupus, but the company’s head of pharma told Fierce that still has a strategy for developing cell therapies for autoimmune disea…
    fiercebiotech · 28d ago
  • ARPA-H puts $160M into bespoke drug therapies; Biohaven switches up scientific leadership
    The ARPA-H program could provide researchers with a roadmap to develop personalized gene editing drugs. Elsewhere, a Botox rival succeeded against migraines and two deals were struck.
    biopharma_dive · 1mo ago
view all news mentions →
brand
EYLEA HD
trade names
Eylea, Yesafili, Zaltrap
generic
AFLIBERCEPT
MOA
12.1 Mechanism of Action Vascular endothelial growth factor-A (VEGF-A) and placental growth factor (PlGF) are members of the VEGF family of angiogenic factors that can act as mitogenic, chemotactic, and vascular permeability factors for endothelial cells. VEGF acts via two receptor tyrosine kinases, VEGFR-1 and VEGFR-2, present on the surface of endothelial cells. PlGF binds only to VEGFR-1, which is also present on the surface of leucocytes. Activation of these receptors by VEGF-A can result in neovascularization and vascular permeability. Aflibercept acts as a soluble decoy receptor that binds VEGF-A and PlGF, and thereby can inhibit the binding and activation of these cognate VEGF receptors.
indication
wet AMD, diabetic macular edema, retinal vein occlusion
phase
marketed
approved
2011-11-18
Data sources
openFDA · ClinicalTrials.gov · OpenTargets
last refreshed 16m ago
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