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Sol-Gel Technologies (SLGL) investor relations material
Sol-Gel Technologies Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Announced Q3 2025 results, highlighting progress in late-stage pipeline for rare dermatologic diseases and expansion of commercial partnerships for approved products.
Health Canada approved EPSOLAY for rosacea; new licensing agreements signed for EPSOLAY and TWYNEO in Australia and New Zealand.
Ongoing pivotal Phase 3 trial for SGT-610 in Gorlin syndrome, with top-line results expected Q4 2026; exploring high-frequency BCC as an additional indication.
Financial highlights
Q3 2025 revenue was $0.4 million, down from $5.4 million in Q3 2024, mainly due to lower licensing and royalty income.
Research and development expenses rose to $5.7 million from $4.8 million year-over-year, driven by SGT-610 development and clinical trial costs.
General and administrative expenses decreased to $1 million from $1.4 million, reflecting cost-saving measures.
Net loss for Q3 2025 was $5.9 million ($2.13 per share), compared to a net loss of $0.4 million ($0.13 per share) in Q3 2024.
Cash, cash equivalents, and marketable securities totaled $20.9 million as of September 30, 2025.
Outlook and guidance
TWYNEO and EPSOLAY expected to launch in most new territories in 2028 and 2027, respectively.
Anticipated annual royalty revenue from these launches could reach $10 million by 2031.
Cash resources projected to fund operations into Q1 2027.
Targeting $10 million EBITDA from ex-U.S. business by 2031.
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