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An Open-label, Single-arm, Multicenter Study in Patients With Neovascular Age-related Macular Degeneration to Evaluate the Safety of SOK583A1 (40 mg/mL), a Proposed Aflibercept Biosimilar Product, Provided in a Prefilled Syringe

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An Open-label, Single-arm, Multicenter Study in Patients With Neovascular Age-related Macular Degeneration to Evaluate the Safety of SOK583A1 (40 mg/mL), a Proposed Aflibercept Biosimilar Product, Provided in a Prefilled Syringe

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 21 Nov 2022

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At a glance

  • Drugs Aflibercept (Primary)
  • Indications Wet age-related macular degeneration
  • Focus Adverse reactions; Registrational
  • Sponsors Sandoz

    • Most Recent Events

    • 25 Jul 2022 Status changed from not yet recruiting to completed.
    • 01 Mar 2022 Planned End Date changed from 30 May 2022 to 20 Jun 2022.
    • 01 Mar 2022 Planned primary completion date changed from 30 May 2022 to 20 Jun 2022.

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