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Clinical Trial Summary

Evaluate the effect of IONIS-FB-LRx on the rate of change of the area of geographic atrophy (GA) secondary to age-related macular degeneration (AMD) measured by fundus autofluorescence (FAF).


Clinical Trial Description

The study will assess the rate of change of the area of GA secondary to AMD by measuring FAF in up to 330 participants with GA due to AMD being treated with IONIS-FB-LRx. The study is a Phase 2, double-masked, randomized, stratified, placebo-controlled study conducted at multiple centers. It is an adaptive design in which three dose levels will be evaluated in a subset of participants (Stage 1) and, following an interim analysis, the number of participants in two of the dose cohorts will be expanded (Stage 2). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03815825
Study type Interventional
Source Ionis Pharmaceuticals, Inc.
Contact
Status Active, not recruiting
Phase Phase 2
Start date March 4, 2019
Completion date June 2024

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