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NASDAQ:CLSD

Clearside Biomedical Q2 2024 Earnings Report

Clearside Biomedical logo
$0.88 +0.01 (+1.07%)
Closing price 07/11/2025 04:00 PM Eastern
Extended Trading
$0.88 -0.01 (-1.12%)
As of 07/11/2025 07:06 PM Eastern
Extended trading is trading that happens on electronic markets outside of regular trading hours. This is a fair market value extended hours price provided by Polygon.io. Learn more.

Clearside Biomedical EPS Results

Actual EPS
-$0.10
Consensus EPS
-$0.14
Beat/Miss
Beat by +$0.04
One Year Ago EPS
-$0.15

Clearside Biomedical Revenue Results

Actual Revenue
$0.09 million
Expected Revenue
$0.25 million
Beat/Miss
Missed by -$160.00 thousand
YoY Revenue Growth
N/A

Clearside Biomedical Announcement Details

Quarter
Q2 2024
Time
After Market Closes
Conference Call Date
Monday, August 12, 2024
Conference Call Time
4:00PM ET

Upcoming Earnings

Clearside Biomedical's Q2 2025 earnings is scheduled for Monday, August 11, 2025, with a conference call scheduled at 4:00 PM ET. Check back for transcripts, audio, and key financial metrics as they become available.

Clearside Biomedical Earnings Headlines

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About Clearside Biomedical

Clearside Biomedical (NASDAQ:CLSD) is a clinical-stage biopharmaceutical company focused on developing and commercializing therapies that leverage its proprietary suprachoroidal space (SCS) drug delivery platform to treat eye diseases. The company’s SCS Microinjector™ enables targeted administration of small molecule and biologic therapies directly to the back of the eye, offering potential benefits in efficacy and safety over conventional intravitreal or systemic approaches. Clearside’s research and development efforts are concentrated on retinal and choroidal disorders that represent significant unmet medical needs, including macular edema, age-related macular degeneration and diabetic retinopathy.

The company’s first approved product, Xipere® (triamcinolone acetonide injectable suspension), is designed for suprachoroidal administration to address macular edema associated with uveitis. In addition to this commercial offering, Clearside maintains a robust pipeline of product candidates, including CLS-AX (axitinib suprachoroidal injectable suspension) for the treatment of neovascular age-related macular degeneration and CLS-301, an anti-VEGF therapy in preclinical development for diabetic macular edema. These programs exemplify the versatility of Clearside’s delivery technology in accommodating both small molecules and larger biologics within the same targeted anatomical space.

Founded in 2009 and headquartered in Alpharetta, Georgia, Clearside has built strategic collaborations and licensing agreements to advance its technology into new markets. The company conducts clinical trials across the United States and in select international locations, fostering partnerships with contract research organizations and academic medical centers. Clearside’s intellectual property portfolio includes multiple issued patents covering the SCS delivery method, as well as key formulation and device innovations that underpin its therapeutic platform.

Under the leadership of Chief Executive Officer Jeff S. Boyer and supported by a management team with deep expertise in ophthalmology, pharmacology and medical device development, Clearside is positioned to address a broad spectrum of posterior segment diseases. The company’s strategic plan emphasizes advancing late-stage clinical candidates, expanding global regulatory submissions and fostering commercial readiness to bring next-generation ocular therapies to physicians and patients worldwide.

View Clearside Biomedical Profile

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