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A Randomized, Double Masked, Active Controlled, Phase 3 Study of the Efficacy, Safety, and Tolerability of Repeated Doses of Intravitreal VEGF Trap in Subjects With Neovascular Age-related Macular Degeneration (AMD)

Trial Profile

A Randomized, Double Masked, Active Controlled, Phase 3 Study of the Efficacy, Safety, and Tolerability of Repeated Doses of Intravitreal VEGF Trap in Subjects With Neovascular Age-related Macular Degeneration (AMD)

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 23 Jul 2019

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At a glance

  • Drugs Aflibercept (Primary) ; Ranibizumab
  • Indications Wet age-related macular degeneration
  • Focus Registrational; Therapeutic Use
  • Acronyms VIEW-2
  • Sponsors Bayer
  • Most Recent Events

    • 31 Aug 2018 Biomarkers information updated
    • 17 Aug 2018 According to Regeneron Pharmaceuticals media release, Based on the second year data from trials (VIEW-1 and VIEW-2) U.S. Food and Drug Administration (FDA) has approved a supplemental Biologics License Application (sBLA) for EYLEA (aflibercept) Injection in patients with wet age-related macular degeneration (wet AMD).
    • 13 Aug 2018 According to Regeneron Pharmaceuticals media release, Based on the second year data from trials (VIEW-1 and VIEW-2) U.S. Food and Drug Administration (FDA) has issued a complete response letter (CRL) regarding the supplemental Biologics License Application (sBLA) for EYLEA (aflibercept) Injection in patients with wet age-related macular degeneration (wet AMD). The company expects to complete these discussions and receive a final FDA action within approximately two months.
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