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A Single-arm, Non-randomized and Open-label Phase 3 Study Evaluating the Efficacy, Safety and Tolerability of Intravitreal Aflibercept in Japanese Patients With Neovascular Glaucoma (NVG)

Trial Profile

A Single-arm, Non-randomized and Open-label Phase 3 Study Evaluating the Efficacy, Safety and Tolerability of Intravitreal Aflibercept in Japanese Patients With Neovascular Glaucoma (NVG)

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 07 Jan 2022

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At a glance

  • Drugs Aflibercept (Primary)
  • Indications Neovascular glaucoma
  • Focus Therapeutic Use
  • Acronyms VENERA
  • Sponsors Bayer
  • Most Recent Events

    • 16 Dec 2020 Results published in the Advances in Therapy
    • 27 Mar 2020 According to a Bayer media release, the company announced that Bayer Yakuhin has received approval for the additional indication of neovascular glaucoma for the intravitreal VEGF inhibitor EYLEAsolution for intravitreal injection 40 mg/mL. This approval is based on the data from two Phase III studies (VEGA and VENERA).
    • 18 Feb 2020 Primary endpoint (Change in IOP (intraocular pressure) from baseline to Week 1) has been met as per results published in the ClinicalTrials.gov Trial Registry

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