MARKET

CLSD

CLSD

Clearside Biomed
NASDAQ
1.130
-0.020
-1.74%
Closed 17:55 07/25 EDT
OPEN
1.150
PREV CLOSE
1.150
HIGH
1.190
LOW
1.120
VOLUME
191.37K
TURNOVER
0
52 WEEK HIGH
2.120
52 WEEK LOW
0.6501
MARKET CAP
84.45M
P/E (TTM)
-2.0810
1D
5D
1M
3M
1Y
5Y
1D
Clearside Biomedical Price Target Maintained With a $4.00/Share by Needham
Dow Jones · 1d ago
Clearside Biomedical’s Promising CLS-AX Treatment in the ODYSSEY Trial: A Buy Rating Based on Safety and Potential Market Impact
TipRanks · 2d ago
Buy Rating Affirmed: Clearside Biomedical’s Innovative Drug Delivery and Promising Clinical Trials
TipRanks · 2d ago
Clearside Biomedical Hosts Suprachoroidal Delivery Webinar
TipRanks · 2d ago
Clearside Biomedical Opens Registration for Suprachoroidal Delivery KOL Webinar to Be Held on Wednesday, July 24, 2024 at 8:00 am ET
Clearside Biomedical, Inc. Has opened registration for its virtual key opinion leader event on July 24, 2024. The company is revolutionizing the delivery of therapies to the back of the eye through the suprachoroidal space. The event will be held in Atlanta, Georgia.
Barchart · 4d ago
Weekly Report: what happened at CLSD last week (0715-0719)?
Weekly Report · 4d ago
Weekly Report: what happened at CLSD last week (0708-0712)?
Weekly Report · 07/15 09:51
CLEARSIDE BIOMEDICAL APPOINTS DR. GLENN YIU TO ITS SCIENTIFIC ADVISORY BOARD
Reuters · 07/11 11:05
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About CLSD
Clearside Biomedical, Inc. is a biopharmaceutical company focused on the delivery of therapies to the back of the eye through the suprachoroidal space (SCS). The Company's SCS injection platform, utilizing its patented SCS Microinjector, enables an in-office, repeatable, non-surgical procedure for the targeted and compartmentalized delivery of a variety of therapies to the macula, retina, or choroid to potentially preserve and improve vision in patients with sight-threatening eye diseases. The Company is developing its own pipeline of small molecule product candidates for administration via its SCS Microinjector. The Company's lead program, CLS-AX (axitinib injectable suspension), for the treatment of neovascular age-related macular degeneration (wet AMD), is in Phase 2b clinical testing. It developed and gained approval for its product, XIPERE (triamcinolone acetonide injectable suspension) for suprachoroidal use, which is available in the United States through a commercial partner.

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