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A Study to Evaluate the Efficacy and Safety of IBI302 in Subjects With nAMD

StatusActive, Not Recruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Start date: Aug 15, 2023 to Sep 21, 2023 Trial status: Recruiting to Active, Not Recruiting · Study site revisedv3 Show 2 more changesShow less
    • Trial status: Recruiting to Active, Not Recruiting
    • Study site revised

    See this version in full on ClinicalTrials.gov ↗

  2. Notable Trial status: Not Yet Recruiting to Recruiting Primary endpoint revised · Site details revisedv2 Show 2 more changesShow less
    • Primary endpoint revised
    • Site details revised

    See this version in full on ClinicalTrials.gov ↗

  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The study is designed for multi-center,randomized,double-masked,active-contralled study to evaluate effective and security of intravitreal injection of IBI302 in subjects with neovascular age-related macular degeneration.
Trial Details
NCT Number NCT05972473
Lead Sponsor Innovent Biologics (Suzhou) Co. Ltd.
Conditions Neovascular Age-related Macular Degeneration
Enrollment 600 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov