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Anebulo Pharmaceuticals (ANEB) investor relations material
Anebulo Pharmaceuticals Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Focused on developing selonabant, a cannabinoid receptor antagonist, for cannabis-induced toxicity, prioritizing pediatric IV formulation due to unmet medical need and regulatory feedback.
Initiated Phase 1 single ascending dose (SAD) study of IV selonabant for acute cannabis-induced toxicity in children, with FDA clearance and NIDA grant support; ongoing observational study in emergency departments.
No product revenue to date; operations funded by equity raises, grants, and a loan facility.
Board approved a proposed reverse stock split as part of a potential going private transaction; process impacted by government shutdown and SEC delays.
Financial highlights
Net loss for the quarter ended September 30, 2025 was $2.16 million, compared to $2.20 million for the same quarter last year; Q1 FY2026 net loss was $2.2 million on $2.3 million in expenses.
Operating expenses decreased to $2.26 million from $2.41 million year-over-year, driven by lower R&D costs.
Cash and cash equivalents were $10.4 million as of September 30, 2025, with access to an additional $3.0 million via a loan agreement.
No revenue recognized; grant income of $809,991 recognized in Q1 FY2026, down from $245,000 year-over-year.
Outlook and guidance
Cash and equivalents, plus available loan facility, expected to fund operations for at least 12 months from the report date.
Ongoing focus on developing selonabant IV for pediatric cannabis toxicity, with support from NIDA and collaboration with FDA.
Anticipates continued operating losses and need for additional capital to advance clinical programs; R&D expenses expected to increase as clinical studies progress.
Board expects to provide further updates on strategic alternatives and the reverse stock split by year-end.
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