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Clearside Biomedical (CLSDQ) investor relations material
Clearside Biomedical Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Focused on suprachoroidal space (SCS) drug delivery, with XIPERE as the first FDA-approved product for uveitic macular edema.
In July 2025, initiated a strategic review, including potential sale, licensing, or other transactions, and transitioned all employees to consulting roles.
Paused all internal R&D programs to conserve cash while seeking strategic alternatives.
Financial highlights
Net loss of $5.97 million for Q3 2025, improved from $7.69 million in Q3 2024; net loss of $18.69 million for the nine months ended September 30, 2025, versus $27.05 million in the prior year period.
License and other revenue was $0.2 million for Q3 2025, down from $1.0 million in Q3 2024; $3.0 million for the nine months, up from $1.4 million in 2024.
Cash and cash equivalents were $6.8 million as of September 30, 2025, down from $20.0 million at year-end 2024.
Operating cash outflow was $16.0 million for the nine months ended September 30, 2025.
Outlook and guidance
Current cash is insufficient to fund operations for the next 12 months; substantial doubt exists about the ability to continue as a going concern.
Exploring strategic alternatives; if unsuccessful, may need to file for bankruptcy or wind down operations.
All internal R&D paused; future activities depend on additional capital or successful strategic transaction.
- TimeTickerHeadlineOpen
- 6 FebWASH
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Net loss widened to 7.5m PLN in H1 2024 as revenue fell and R&D costs remained high.
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