Infographic: efficacy and safety of intravitreal siRNA therapy for acute NAION (QRK207 trial)

Fig. 1 Full size image QPI-1007 is a short-interfering RNA molecule that inhibits the expression of caspase 2, an endopeptidase that is involved in retinal ganglion cell death [ 1 ]. This infographic summarises the design and results of the phase II/III multicentre trial, which evaluated the efficacy and safety of QPI-1007 in patients with acute non-arteritic anterior ischemic optic neuropathy (NAION) [ 1 ]. QPI-1007 was well-tolerated. There was no statistically significant difference between the active treatment cohorts (QPI-1007) and the sham (placebo) group in the proportion of patients who lost ≥15 ETDRS letters of BCVA at 6 months [ 1 ]. Over 30% of participants experienced vision deterioration within the first three weeks of the study (from screening day to intervention) [ 2 ]. Frequency of traditional vascular risk factors for NAION development among participants were found to be similar to that of the general population [ 3 ].

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Journal
Eye
Published
2026-06-24
DOI
https://doi.org/10.1038/s41433-026-04670-3
Primary Topic
Intraoperative Neuromonitoring and Anesthetic Effects
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article
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article

Infographic: efficacy and safety of intravitreal siRNA therapy for acute NAION (QRK207 trial)

Shreyas Bhat, Susan P. Mollan, Gabriele Berman, Michael Lowe
Eye
Intraoperative Neuromonitoring and Anesthetic Effects
article

Infographic: efficacy and safety of intravitreal siRNA therapy for acute NAION (QRK207 trial)

Shreyas Bhat, Susan P. Mollan, Gabriele Berman, Michael Lowe
article en

Abstract

Fig. 1 Full size image QPI-1007 is a short-interfering RNA molecule that inhibits the expression of caspase 2, an endopeptidase that is involved in retinal ganglion cell death [ 1 ]. This infographic summarises the design and results of the phase II/III multicentre trial, which evaluated the efficacy and safety of QPI-1007 in patients with acute non-arteritic anterior ischemic optic neuropathy (NAION) [ 1 ]. QPI-1007 was well-tolerated. There was no statistically significant difference between the active treatment cohorts (QPI-1007) and the sham (placebo) group in the proportion of patients who lost ≥15 ETDRS letters of BCVA at 6 months [ 1 ]. Over 30% of participants experienced vision deterioration within the first three weeks of the study (from screening day to intervention) [ 2 ]. Frequency of traditional vascular risk factors for NAION development among participants were found to be similar to that of the general population [ 3 ].

Eye
University Hospitals Birmingham NHS Foundation Trust (GB), Queen's University (CA), Queen Elizabeth University Hospital (GB), University of Birmingham (GB), McMaster University (CA)
Good health and well-being
Openalex Percentile: Top 6%
Intraoperative Neuromonitoring and Anesthetic Effects
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