
Part I: Financial Information Financial Statements The unaudited condensed consolidated financial statements for Q1 2025 reflect a net loss, increased revenue, and decreased assets and cash, indicating continued reliance on financing Condensed Consolidated Balance Sheets As of April 30, 2025, total assets decreased to $6.15 million from $7.47 million, primarily due to reduced cash, while liabilities remained stable and equity decreased Condensed Consolidated Balance Sheet Highlights (in USD) | Account | April 30, 2025 (Unaudited) | January 31, 2025 | | :--- | :--- | :--- | | Assets | | | | Cash and cash equivalents | $2,964,097 | $4,311,719 | | Total Current Assets | $3,429,647 | $4,794,265 | | Goodwill | $1,719,535 | $1,719,535 | | Total Assets | $6,152,181 | $7,469,955 | | Liabilities & Equity | | | | Total Current Liabilities | $925,051 | $982,845 | | Total Liabilities | $1,048,795 | $1,041,050 | | Total Stockholders' Equity | $5,103,386 | $6,428,905 | Condensed Consolidated Statements of Operations For the three months ended April 30, 2025, revenue increased by 63% to $667,432, with the net loss improving to $1.39 million due to lower operating expenses Consolidated Statements of Operations (in USD) | Metric | Three Months Ended April 30, 2025 | Three Months Ended April 30, 2024 | | :--- | :--- | :--- | | Revenue | $667,432 | $408,532 | | Cost of revenues | $415,451 | $243,746 | | Research and development | $683,426 | $974,535 | | Selling, general and administrative | $982,052 | $1,079,728 | | Loss from operations | $(1,413,497) | $(1,889,477) | | Net loss | $(1,388,869) | $(1,898,077) | | Net loss per share (basic and diluted) | $(0.12) | $(0.21) | Condensed Consolidated Statements of Cash Flows For the three months ended April 30, 2025, net cash used in operating activities increased, resulting in a $1.35 million net decrease in cash, ending the period with $2.96 million Consolidated Statements of Cash Flows (in USD) | Cash Flow Activity | Three Months Ended April 30, 2025 | Three Months Ended April 30, 2024 | | :--- | :--- | :--- | | Net Cash Used In Operating Activities | $(1,336,972) | $(833,926) | | Net Cash Used in Investing Activities | $(5,324) | $(6,195) | | Net Cash Provided by Financing Activities | $(5,326) | $8,694,919 | | Net change in cash | $(1,347,622) | $7,854,798 | | Cash and cash equivalents - End of period | $2,964,097 | $8,347,740 | Notes to Unaudited Condensed Consolidated Financial Statements The notes detail the company's business structure, accounting policies, and financial components, covering transdermal products, going concern, revenue recognition, and legal contingencies - The company's primary business is the development of transdermal pharmaceutical products, focusing on its Aversa abuse-deterrent technology, with revenue generated through Pocono Pharmaceuticals and 4P Therapeutics2123107 - Management believes recent equity financing of $8.4 million in April 2024 and a $5 million related-party credit line alleviate substantial doubt about the company's ability to continue as a going concern, despite historical operating losses2829 - All revenue for the three months ended April 30, 2025 and 2024, was generated from the sale of goods within the United States39 - The company is a defendant in a lawsuit with Joseph Gunnar, LLC, and Lucosky Brookman LLP, who are seeking over $500,000 in damages, with the company denying allegations and filing counterclaims; a $100,000 settlement offer from plaintiffs has not been responded to99100101 - The company signed an amended agreement with Kindeva Drug Delivery for Aversa Fentanyl, reducing labor rates in exchange for a $3.0 million milestone payment upon FDA approval96 Management's Discussion and Analysis of Financial Condition and Results of Operations Management attributes Q1 2025 revenue growth to increased demand, with a narrowed net loss due to reduced expenses, and believes recent financing alleviates going concern doubts Results of Operations Comparison (in USD) | Metric | Three Months Ended April 30, 2025 | Three Months Ended April 30, 2024 | | :--- | :--- | :--- | | Revenue | $667,432 | $408,532 | | Gross Profit | $251,981 | $164,786 | | R&D Expenses | $683,426 | $974,535 | | SG&A Expenses | $982,052 | $1,079,728 | | Net Loss | $(1,388,869) | $(1,898,077) | - Revenue increase was driven by the Pocono Pharmaceuticals segment due to new equipment meeting increased demand, while the 4P Therapeutics segment generated no revenue117 - The decrease in R&D expenses is primarily due to a reduction in labor costs for the Aversa Fentanyl product development119 - The company's cash and cash equivalents decreased from $4.31 million at Jan 31, 2025, to $2.96 million at April 30, 2025, with working capital also decreasing from $3.81 million to $2.50 million121 - In April 2024, the company completed an $8.4 million equity financing with European investors to fund operations and development111116 Quantitative and Qualitative Disclosures about Market Risk This section is not applicable for the company at the time of filing - The company has indicated that this item is not applicable152 Controls and Procedures Management concluded that disclosure controls and procedures were not effective due to material weaknesses, but remediation efforts are underway - The CEO and CFO concluded that disclosure controls and procedures are not effective154 - Material weaknesses identified include the absence of segregation of duties and lack of qualified accounting personnel155 - Remediation efforts include adding qualified accounting personnel to reduce reliance on third-party consultants and improving internal controls for transaction reviews155 Part II: Other Information Legal Proceedings The company is a defendant in a lawsuit seeking over $500,000 in damages, denies all allegations, has filed counterclaims, and has not responded to a settlement offer - The company is a defendant in a lawsuit filed by Joseph Gunnar, LLC and Lucosky Brookman LLP in New York160 - Allegations include breach of contract, fraudulent activities, and tortious interference, with Gunnar seeking over $500,000 in damages and LB seeking reimbursement of legal fees160 - Nutriband denies all allegations and has filed counterclaims for intentional interference and breach of fiduciary duty, seeking $1,000,000 for each claim161 - The plaintiffs proposed a settlement offer of $100,000 in early 2024, to which the company has not responded162 Risk Factors The company highlights key risks including economic uncertainty, its pre-market development stage, stock price volatility, potential dilution, and the need to keep pace with technological change - The company faces risks from economic uncertainty and U.S. administration policies that could affect costs and FDA approval timelines164 - As a development-stage company with no marketable product in the U.S., there is no assurance of achieving profitability, and the company has a history of substantial losses165166 - The company's stock price has been and is expected to remain volatile, and future equity offerings may cause significant dilution to existing stockholders169170 - The drug delivery industry is subject to rapid technological change, and a failure to keep pace could render the company's products obsolete171 Exhibits This section lists the exhibits filed with the Form 10-Q, including CEO and CFO certifications and Inline XBRL data files Filed Exhibits | Exhibit Number | Description | | :--- | :--- | | 31.1 | Section 302 Certification of Chief Executive Officer | | 31.2 | Section 302 Certification of Chief Financial Officer | | 32.1 | Section 906 Certification of Chief Executive Officer | | 32.2 | Section 906 Certification of Chief Financial Officer | | 101 | Inline XBRL Documents (Instance, Schema, Calculation, etc.) |