OCUL
Ocular Therapeutix, Inc.14.39
+0.22+1.55%
Dec 16, 4:00:00 PM EST
Earnings Call Transcripts
This Quarter (Q1 '26)
No earnings call transcript available yet
Last Quarter (Q4 '25)
No earnings call transcript available
Key Stats
Market Cap
3.07BP/E (TTM)
-Basic EPS (TTM)
-1.43Dividend Yield
0%Recent Filings
8-K
NDA shift on single Phase 3
10-Q
Q3 FY2025 results
Ocular Therapeutix posted Q3 revenue of $14.5M, down 5% y/y from $15.4M yet with in-market DEXTENZA units up 6,000 to 48,000 amid Medicare reimbursement pressures. R&D surged 41% y/y to $52.4M, driven by $34.7M on AXPAXLI wet AMD trials (SOL-1, SOL-R), fueling a $68.7M operating loss—wider than $46.0M y/y—while net loss hit $69.4M versus $36.5M, the gap due to fair-value changes in derivative liabilities. Cash sits at $344.8M with $70.6M net debt (Barings term loan due 2029); October's $445M offering bolsters runway. SOL-1 nears Q1 2026 readout. Clinical trial delays loom large.
8-K
Q3 results: revenue dips, trials advance
Ocular Therapeutix reported Q3 net revenue of $14.5M, down 5.8% from $15.4M last year due to DEXTENZA reimbursement headwinds, yet unit sales rose 9.7% sequentially. R&D expenses jumped to $52.4M from $37.1M amid SOL-1/SOL-R trials; SOL-R hit 555-subject target with topline data on track for 1H 2027. Cash stands at $344.8M plus ~$445M from October offering. Runway extends into 2028.
8-K
OCUL prices $446M stock offering
Ocular Therapeutix priced an underwritten offering of 37,909,018 common shares at $12.53 each on September 30, 2025, expecting to close October 1 and raise net proceeds of $445.9 million. The funds will support AXPAXLI's open-label extension for wet AMD, Phase 3 trials for NPDR, manufacturing investments, and pre-commercialization efforts. Cash runway extends into 2028, yet excludes full AXPAXLI launch costs. Assumptions may falter.
8-K
AXPAXLI program updates announced
Ocular Therapeutix announced updates on September 30, 2025, for its AXPAXLI program targeting wet AMD and NPDR. The SOL-1 Phase 3 trial completed randomization of 344 subjects and boasts over 95% retention with no new safety signals; topline data expected Q1 2026. SOL-R enrollment finished, results due first half 2027. Plans for HELIOS-2 and HELIOS-3 Phase 3 trials in NPDR secured FDA SPA agreements. A new U.S. patent allowance extends IP to 2044. Trials advance, but outcomes remain uncertain.
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