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Artelo Biosciences (ARTL) investor relations material
Artelo Biosciences Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Clinical-stage biopharma focused on lipid-signaling therapeutics, with no revenue to date and continued operating losses; net loss of $5.6M for the six months ended June 30, 2025.
Pipeline includes ART27.13 (cancer-related anorexia, Phase 2a), ART26.12 (FABP5 inhibitor, Phase 1), and ART12.11 (CBD cocrystal); ART26.12 completed Phase 1 SAD study, MAD study planned for Q4 2025.
ART12.11 preclinical data showed efficacy in depression and cognitive function; first-in-human study planned for H1 2026.
Adopted a Digital Asset Treasury (DAT) strategy, allocating significant capital to Solana (SOL) cryptocurrency as a non-core treasury reserve asset.
Financial highlights
Net loss of $3.2M for Q2 2025, up from $2.4M in Q2 2024; net loss of $5.6M for the six months ended June 30, 2025.
Operating expenses for Q2 2025 were $3.2M, up from $2.5M year-over-year, driven by higher R&D and professional fees.
R&D expenses were $1.9M and G&A expenses $1.3M for Q2 2025, both increased year-over-year.
Cash and cash equivalents were $2.1M as of June 30, 2025, down from $2.3M at year-end 2024.
Working capital deficit of $3.5M as of June 30, 2025, compared to positive $0.8M at December 31, 2024.
Outlook and guidance
Substantial doubt exists about the ability to continue as a going concern within one year without additional funding.
Ongoing pursuit of equity or debt financing and licensing opportunities; no assurance of success.
R&D and G&A expenses expected to remain at or above current levels as clinical programs advance.
Multiple clinical data announcements anticipated in Q3 2025, including initial data from Phase 2 CARES study (ART27.13).
ART26.12 advancing to MAD study in Q4 2025; ART12.11 first-in-human trial expected in H1 2026.
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