Enveric Biosciences Inc Dossier
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SectorHealth Care IndustryBiotechnology Beta (adjusted)1.09 Intrinsic Value Insufficient data for a value estimateNot enough reliable inputs to publish a fair value for this company yet. Market Price $1.46Price as of 1 Oct 2026 Data confidenceNot applicable Market Cap $6.5M Enterprise Value $2.3M Shares Outstanding 4.5M diluted Next Earnings Date13 Nov 2026 Last ex-dividend23 Apr 2008 All prices and values are periodic snapshots, not live quotes. Source dates are shown for reference. ThesisStreet consensus, scenarios, merits, risks, and invalidation triggers Thesis Summary Enveric Biosciences is a pre-revenue biotechnology company focused on developing next-generation, non-hallucinogenic neuroplastogenic small-molecule therapeutics (such as lead asset EB-003) for neuropsychiatric disorders. While the company has successfully extended its cash runway into Q1 2027 through recent private placements and ATM offerings, it remains a highly speculative micro-cap with ongoing going-concern risks. The streamlined regulatory path recommended by the FDA for EB-003 and strong IP protection are positive drivers, but investors should maintain a Hold stance until the IND is formally cleared and Phase 1 clinical trials begin. This section is the 12-month view: analyst targets and the probability-weighted scenarios built from them. The intrinsic value at the top of this page answers a different question: what the business is worth today. Our research · scenarios, merits, risks, and invalidation triggersResearch as of 20 Jun 2026 Scenarios · 12-month scenario targets Bear CaseDownside scenario $0.5020% IND-enabling genotoxicity studies reveal safety concerns, or the FDA places a clinical hold on the EB-003 application. Capital markets tighten, preventing Enveric from raising additional funds, which accelerates going-concern distress and forces highly dilutive equity issuances or a reverse stock split. Base CaseCentral scenario $2.0055% Enveric completes remaining IND-enabling studies for EB-003 and submits the IND application to the FDA in late 2026. The company continues to fund operations through incremental dilution via its ATM facility, maintaining its speculative profile as it prepares for Phase 1 clinical entry. Bull CaseUpside scenario $5.0025% The FDA clears the IND for EB-003 without delay, allowing Enveric to initiate Phase 1 trials by late 2026. The non-hallucinogenic profile of EB-003 is clinically validated, attracting a major pharmaceutical out-licensing partner and securing non-dilutive upfront milestone payments that resolve going-concern issues. Scenarios reflect our research view at the research date. Key Investment Merits
Key Investment Risks
Thesis Invalidation Triggers
All scenarios are estimates and subject to change. Past performance is not indicative of future results. Quality Pillars MembersThis section is available to registered members. Create a free account or sign in to unlock the full breakdown. Explore this dossierValuationIntrinsic value, the six-method breakdown, peer medians, and your assumptions sandbox.Financial SnapshotRevenue, profitability, returns, balance sheet, dividends, and the filing-level detail.Qualitative AnalysisBusiness overview, strategic initiatives, and mergers, acquisitions & partnerships.Outlook & Key DatesForward estimates, reporting calendar, and the monitoring framework. |