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Clinical Trial Summary

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 IRIS Registry, and all results were based on the study period from 01/01/2019 to 12/31/2019.


Clinical Trial Description

This was a retrospective cohort study of eyes in adult patients with a diagnosis of wet AMD who were treated with anti-VEGF agents from 01/01/2019 to 12/31/2019. IRIS Registry data from 01/01/2019 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: 01/01/2019 to 12/31/2019 - Pre-index period: 01/01/2018 to 12/31/2018 - Post-index period: 01/01/2019 to 12/31/2019 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05110209
Study type Observational
Source Novartis
Contact
Status Completed
Phase
Start date July 15, 2020
Completion date November 20, 2020

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