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NASDAQ:IRD

Opus Genetics Q4 2024 Earnings Report

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$5.41 -0.41 (-7.04%)
Closing price 09/16/2026 04:00 PM Eastern
Extended Trading
$5.52 +0.11 (+2.11%)
As of 07:42 AM Eastern
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Opus Genetics EPS Results

Actual EPS
-$1.27
Consensus EPS
-$0.34
Beat/Miss
Missed by -$0.93
One Year Ago EPS
N/A

Opus Genetics Revenue Results

Actual Revenue
$3.40 million
Expected Revenue
$11.10 million
Beat/Miss
Missed by -$7.70 million
YoY Revenue Growth
N/A

Opus Genetics Announcement Details

Quarter
Q4 2024
Time
Before Market Opens
Conference Call Date
Monday, March 31, 2025
Conference Call Time
7:00AM ET

Upcoming Earnings

Opus Genetics' Q3 2026 earnings is estimated for Wednesday, November 11, 2026, based on past reporting schedules, with a conference call scheduled on Thursday, November 12, 2026 at 12:30 PM ET. Check back for transcripts, audio, and key financial metrics as they become available.

Opus Genetics Earnings Headlines

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About Opus Genetics

Opus Genetics (NASDAQ:IRD) is a clinical-stage biotechnology company focused on developing gene therapies for inherited retinal diseases (IRDs), a group of rare genetic disorders that can cause progressive vision loss or blindness. The company aims to address conditions for which treatment options are limited or unavailable by developing therapies designed to correct or replace disease-causing genetic defects in retinal cells.

Opus Genetics’ pipeline includes investigational programs for genetically defined retinal disorders, including rhodopsin-associated autosomal dominant retinitis pigmentosa and BEST1-related retinal disease. Its programs are intended to use gene therapy approaches to deliver functional genetic material to affected retinal tissues. The company’s assets remain in the research and clinical-development stages and are not broadly marketed commercial products.

Opus Genetics was established in 2021 and has pursued the development of treatments for rare ophthalmic diseases through internal research and collaborations. The company is headquartered in the United States and focuses primarily on advancing potential therapies through preclinical and clinical testing for patients with inherited retinal diseases.

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