Source document
Income flow
| Revenue — GREEN | $56.3M | +137.8% YoY |
|---|---|---|
| Gross margin — GREEN | 94.5% | |
| Net income — GREEN | -$123.0M | -56.0% YoY |
| Net margin — GREEN | -218.2% | |
| Operating margin — RED | -215.9% |
operating_cf_burnnet_margin_sharply_negativecash_conversion_weakcash_runway_lowaccumulated_deficit_highsbc_revenue_high| Metric | Value | Flag |
|---|---|---|
| EPS (diluted) | $-1.24 | GREEN |
| Gross Margin | 94.5% | GREEN |
| Net Income | -$123.0M | GREEN |
| Net Margin | -218.2% | GREEN |
| Operating Margin | -215.9% | RED |
| R&D % Revenue | 16.0% | GREEN |
| Revenue | $56.3M | GREEN |
| Revenue (quarter) | $33.7M | GREEN |
| Metric | Value | Flag |
|---|---|---|
| Broad Liquidity | $143.8M | GREEN |
| Cash | $8.2M | GREEN |
| Current Ratio | 3.48 | GREEN |
| Debt/Equity | 7.73 | GREEN |
| Total Assets | $249.5M | GREEN |
| Total Equity | $12.5M | GREEN |
| Metric | Value | Flag |
|---|---|---|
| Cash Conversion (CFO/Rev) | -1.88 | GREEN |
| Free Cash Flow | -$105.9M | GREEN |
| Operating CF | -$105.9M | GREEN |
| SBC % Revenue | 35.2% | GREEN |
Sections in this filing
MD&A
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations You should read the following discussion and analysis together with our unaudited condensed consolidated financial statements and related notes thereto included in “Item 1. Financial Statements (Unaudited)” of this Quarterly Report on Form 10-Q and the audited financial statements and related notes thereto as of and for the year ended December 31, 2025 included in our Annual Report on Form 10-K, filed with the Securities and Exchange Commission (“SEC”), on March 9, 2026. Some of the information contained in this discussion and analysis or set forth elsewhere in this Quarterly Report, including information with respect to our plans and strategy for our business, includes forward-looking statements that involve risks and uncertainties. For a complete discussion of forward-looking statements, see the section above entitled “Special Note Regarding Forward-Looking Statements.” As a result of many factors, including those factors set forth under the caption “Item 1A. Risk Factors” of this Quarterly Report, our actual results could differ materially from the results described in or implied by the forward-looking statements contained in the following discussion and analysis. You should carefully read the “Risk Factors” section of this Quarterly Report to gain an understanding of the various factors that could cause actual results to differ materially from our forward-looking statements. Overview We are a biopharmaceutical company focused on the commercialization of neffy ® (also identified in the European Union (“EU”) and United Kingdom (“UK”) by the trade name EURneffy and in China by the trade name 优敏速 ) needle-free intranasal delivery of epinephrine for emergency treatment of Type I allergic reactions, including anaphylaxis. neffy is the first and only needle-free epinephrine product approved by the U.S. Food and Drug Administration (“FDA”) and the European Commission, and also has approvals in the UK, Japan, Australia, China, and Canada. It is the first new delivery method for epinephrine in more than 35 years. neffy is a proprietary composition of epinephrine with an innovative absorption enhancer called Intravail, which allows neffy to safely provide intranasal delivery of epinephrine at a low dose within the exposures of approved injectable products across a range of