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Anebulo Pharmaceuticals (ANEB) investor relations material
Anebulo Pharmaceuticals Q4 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Q4 2025 earnings summary29 Sep, 2025
Executive summary
Initiated Phase 1 SAD study of IV selonabant for acute cannabis-induced toxicity in children, with FDA clearance and NIDA grant support.
Prioritized IV selonabant for pediatric use over adult oral formulation, aiming for faster approval due to higher risk in children.
Board approved a proposed reverse stock split as part of a potential going private transaction, pending shareholder approval.
Financial highlights
Q4 FY25 operating expenses rose to $2.3M from $1.3M year-over-year; net loss was $2.1M ($0.05/share) vs. $1.3M ($0.05/share) prior year.
FY25 operating expenses increased to $9.2M from $8.3M; net loss was $8.5M ($0.25/share) vs. $8.2M ($0.32/share) in FY24.
Cash and equivalents stood at $11.6M as of June 30, 2025, with access to an additional $3M via a loan agreement.
Grant income of $0.9M from NIDA partially offset increased R&D expenses.
Outlook and guidance
Research and development expenses expected to rise as current IV selonabant study completes and further clinical trials are prepared.
Strategic review process ongoing; no set deadline or assurance of outcome.
What supports faster IV pediatric approval?
Future strategy post-reverse stock split?
Scope of FDA collaboration for selonabant?
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Next Anebulo Pharmaceuticals earnings date
Q1 202612 Nov, 2025
Next Anebulo Pharmaceuticals earnings date
Q1 202612 Nov, 2025
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Frequently asked questions
Anebulo Pharmaceuticals, Inc. is a clinical-stage biotechnology company focused on developing treatments for acute cannabinoid intoxication (ACI) and substance abuse. Its primary product candidate, ANEB-001, is a cannabinoid receptor antagonist aimed at rapidly reversing the effects of cannabinoid overdose. The company is headquartered in Lakeway, Texas, and its shares are listed on the Nasdaq.
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