Real-world Evaluation of Prevalence of Ocular Adverse Events in Patients With Neovascular (Wet) Age-related Macular Degeneration (AMD) Who Received Anti-vascular Endothelial Growth Factor (VEGF) Agents (Komodo Health)

Age-related Macular Degeneration (AMD) Clinical Trial

Official title: Real-world Evaluation of Prevalence of Ocular Adverse Events in Patients With Neovascular (Wet) Age-related Macular Degeneration (AMD) Who Received Anti-vascular Endothelial Growth Factor (VEGF) Agents (Komodo Health)

Status Completed

Clinical Trial Summary

This was the cross-sectional study to assess the period prevalence of IOI in patients with wet AMD who were treated with anti- VEGF agents (excluding brolucizumab) over a one-year period in 2019.

Clinical Trial Description

In this cross-sectional study of patients with wet AMD who received ≥1 anti-VEGF injection (excluding brolucizumab), evidence was generated to describe the period prevalence of specific ocular AEs. The study was conducted using the Komodo Healthcare Map, and all results were based on the study period from 01/01/2018 to 12/31/2019.

Komodo Healthcare Map data from 01/01/2018 to 12/31/2019 for patients with a diagnosis of wet AMD who were treated with ≥1 anti-VEGF agent (excluding brolucizumab) were included.

• Identification period: Patients fulfilling the selection criteria during the period from 01/01/2019 to 12/31/2019 were identified

• Index date: 01/01/2019

• Study Period: 01/01/2018 to 12/31/2019

• Pre-index period: 01/01/2018 to 12/31/2018

• Post-index period: 01/01/2019 to 12/31/2019 ;

Related Conditions & MeSH terms

• Age-related Macular Degeneration (AMD)
• Macular Degeneration

• NCT number: NCT05146687
• Study type: Observational
• Source: Novartis
• Status: Completed
• Start date: July 15, 2020
• Completion date: December 11, 2020