- Net Sales: ¥395M
- Operating Income: ¥-1.55B
- Net Income: ¥-1.59B
- EPS: ¥-83.76
| Item | Current | Prior | YoY % |
|---|
| Net Sales | ¥395M | ¥487M | -18.9% |
| Cost of Sales | ¥123M | - | - |
| Gross Profit | ¥364M | - | - |
| SG&A Expenses | ¥1.94B | - | - |
| Operating Income | ¥-1.55B | ¥-1.58B | +1.7% |
| Non-operating Income | ¥25M | - | - |
| Non-operating Expenses | ¥26M | - | - |
| Ordinary Income | ¥-1.59B | ¥-1.58B | -0.7% |
| Income Tax Expense | ¥4M | - | - |
| Net Income | ¥-1.59B | - | - |
| Net Income Attributable to Owners | ¥-1.60B | ¥-1.59B | -0.8% |
| Total Comprehensive Income | ¥-1.62B | ¥-1.59B | -2.1% |
| Interest Expense | ¥2M | - | - |
| Basic EPS | ¥-83.76 | ¥-90.52 | +7.5% |
| Dividend Per Share | ¥0.00 | ¥0.00 | - |
| Item | Current End | Prior End | Change |
|---|
| Current Assets | ¥2.74B | - | - |
| Cash and Deposits | ¥2.11B | - | - |
| Accounts Receivable | ¥87M | - | - |
| Inventories | ¥108M | - | - |
| Non-current Assets | ¥34M | - | - |
| Item | Value |
|---|
| Net Profit Margin | -405.1% |
| Gross Profit Margin | 92.2% |
| Current Ratio | 1227.9% |
| Quick Ratio | 1179.4% |
| Debt-to-Equity Ratio | 0.34x |
| Interest Coverage Ratio | -646.25x |
| Item | YoY Change |
|---|
| Net Sales YoY Change | -18.8% |
| Item | Value |
|---|
| Shares Outstanding (incl. Treasury) | 19.15M shares |
| Treasury Stock | 11K shares |
| Average Shares Outstanding | 19.10M shares |
| Book Value Per Share | ¥45.14 |
| Item | Amount |
|---|
| Q2 Dividend | ¥0.00 |
| Year-End Dividend | ¥0.00 |
| Segment | Revenue | Operating Income |
|---|
| DrugDiscovery | - | ¥-1.49B |
| DrugDiscoverySupport | ¥395M | ¥-64M |
| Item | Forecast |
|---|
| Net Sales Forecast | ¥722M |
| Operating Income Forecast | ¥-2.13B |
| Ordinary Income Forecast | ¥-2.14B |
| Net Income Attributable to Owners Forecast | ¥-2.15B |
| Basic EPS Forecast | ¥-112.46 |
| Dividend Per Share Forecast | ¥0.00 |
This data was automatically extracted from XBRL files. Please refer to the original disclosure documents for accuracy.
Karuna BioScience (4572) reported FY2025 Q3 consolidated results under JGAAP showing a revenue decline to ¥395m (-18.8% YoY) and a substantial ordinary loss of ¥1,590m, consistent with a development-stage biotech cost structure. Net loss was ¥1,600m (EPS -¥83.76), translating to a deeply negative net margin of -405.1%. DuPont analysis indicates ROE of -185.2%, driven by severe negative profitability, modest asset turnover (0.257x), and moderate leverage (assets/equity ≈ 1.78x). The company posted operating loss of ¥1,551m, suggesting that R&D and SG&A expenses far outstrip current revenue capacity. Reported gross profit of ¥364m implies a gross margin of 92.2% on ¥395m of revenue, indicative of high-margin licensing, collaboration, or research service revenue; however, this conflicts with the disclosed cost of sales (¥123m), indicating possible classification or data extraction mismatches. Liquidity appears very strong at face value (current ratio 1,227.9%, quick ratio 1,179.4%), with working capital of ¥2,515m, though the balance sheet shows current assets (¥2,738m) exceeding total assets (¥1,535m), pointing to cross-period or taxonomy inconsistencies. Total liabilities are modest at ¥297m, implying low financial leverage in absolute yen terms, with a debt-to-equity ratio of 0.34x. Interest expense is minor (¥2.4m), and interest coverage is deeply negative (-646x) due to the operating loss. Cash flow statement items are unreported (zeros), limiting assessment of operating cash burn and runway. No dividends were paid (DPS ¥0), consistent with loss-making R&D-phase biopharma. Without cash and share data, per-share capital metrics and runway analysis cannot be precisely determined. The results profile is consistent with a pipeline-focused biotech relying on milestone or licensing revenue, with inherently volatile topline and structurally negative operating leverage until major value inflection points. Revenue contraction underscores dependency on limited, non-recurring streams and timing of contracts. While solvency risks appear muted near term given low liabilities, sustainability hinges on cash reserves and access to external funding. Overall, the financial picture reflects typical early/mid-stage biotech risks: heavy R&D spend, negative earnings, uncertain revenue cadence, and reliance on financing or partnerships.
ROE of -185.2% is explained by net margin of -405.1%, asset turnover of 0.257x, and financial leverage of 1.78x (DuPont). Gross margin based on reported gross profit and revenue is 92.2%, implying high-value, low-cost revenue (e.g., licensing or research services), though the cost of sales figure reported (¥123m) does not reconcile, suggesting categorization timing issues. Operating margin is -392.7% (operating loss ¥1,551m / revenue ¥395m), indicating heavy operating expenses, likely R&D-driven. Ordinary margin is -402.5%, with minimal impact from financing costs (interest ¥2.4m). Effective tax impact is negligible in the loss position (tax ¥3.9m). Operating leverage is acutely negative: small revenue base cannot absorb fixed R&D/SG&A, so incremental revenue growth would need to be sizable to approach breakeven. The negative interest coverage (-646x) is mechanical and reflects the operating loss rather than debt stress. EBITDA is unreported; given depreciation is unreported, EBIT approximates operating loss at -¥1,551m for directional analysis.
Revenue declined 18.8% YoY to ¥395m, consistent with variability in milestone/licensing or project-based revenue. The high implied gross margin suggests quality of revenue is favorable when booked, but sustainability is low due to lumpy recognition and limited recurring components. Profit deterioration is pronounced at the operating and net levels, with losses broadly flat YoY per disclosure commentary (+0.0% YoY notation). Near-term growth hinges on pipeline progress, new collaborations, and milestone triggers rather than volume expansion. With asset turnover at 0.257x, current asset intensity is high relative to revenue, typical for R&D businesses. Outlook: absent material partnership income or out-licensing events in Q4, FY breakeven is unlikely; risk to the topline remains timing-related. Watch for catalysts such as clinical data readouts, licensing deals, or technology-platform monetization to drive step-ups in revenue. Expense discipline and prioritization of programs will be key to moderating cash burn and improving operating leverage.
Liquidity appears robust on reported ratios: current assets ¥2,737.7m vs current liabilities ¥223.0m yields a current ratio of 12.28x and quick ratio of 11.79x, suggesting ample coverage of near-term obligations. Working capital stands at ¥2,514.8m, providing operational buffer. However, total assets are reported at ¥1,535.0m, which is below current assets, indicating reporting or extraction inconsistencies; interpretation should be cautious. Solvency: total liabilities are low at ¥296.8m against equity of ¥864.0m, implying a debt-to-equity ratio of ~0.34x and limited balance sheet leverage. Equity ratio is unreported; based on non-zero data, an indicative equity ratio would be equity/total assets ≈ 56% if total assets are correctly stated at ¥1,535m, but this cannot be confirmed due to inconsistencies. Interest burden is minimal (¥2.4m), and there is no sign of near-term refinancing pressure from the provided data. Overall capital structure is conservative in nominal debt terms, but sustainability depends on cash on hand and future funding access.
Cash flow disclosure items are unreported (Operating, Investing, and Financing CF all shown as 0), preventing a direct assessment of earnings-to-cash conversion, burn rate, and free cash flow. The OCF/Net Income ratio and FCF figures are therefore not interpretable for quality analysis. Given the large operating loss (¥1,551m), underlying operating cash outflow is likely significant, driven by R&D and SG&A, but the magnitude and working capital effects are unknown. Working capital appears positive and large on paper, but with cash and equivalents unreported, liquidity composition is unclear (e.g., cash vs. receivables vs. marketable securities). Without depreciation data, the gap between EBITDA and operating income cannot be assessed. In sum, earnings quality cannot be validated, and FCF cannot be computed with the available data.
No dividend was paid (DPS ¥0), which is consistent with a loss-making R&D-focused profile and capital preservation needs. Payout ratio is effectively 0% due to negative earnings, but this is not informative for sustainability. With FCF unreported and operating losses substantial, any prospective dividends would not be covered by internally generated cash. Typical policy for development-stage biopharma is to refrain from dividends until sustained profitability or stable cash inflows from marketed products/licensing. Near- to medium-term dividend initiation appears unlikely absent a significant shift in cash generation from partnerships or asset monetization.
Business Risks:
- Clinical development and regulatory risk across the pipeline affecting timing and probability of success
- Revenue concentration and lumpiness from milestones, licensing, or limited customers
- Dependence on partner decisions and contract timing for revenue recognition
- Competitive dynamics in target indications and kinase/inhibitor or platform spaces
- IP protection and freedom-to-operate uncertainties
- Talent retention and specialized R&D capability requirements
Financial Risks:
- Sustained operating losses requiring ongoing external financing or dilution
- Uncertainty around cash balance and runway due to unreported cash flow and cash data
- Potential covenant or liquidity risks if contingent liabilities or off-balance items exist (not observable)
- Foreign exchange exposure if partnerships or trials involve foreign currency cash flows
- Budget overrun risk in clinical trials leading to higher-than-planned cash burn
Key Concerns:
- Large operating loss (¥1,551m) versus small revenue base (¥395m)
- Data inconsistencies: current assets (¥2,738m) exceed total assets (¥1,535m); gross profit does not reconcile with cost of sales
- Lack of disclosed cash and cash flow details, limiting runway assessment
- High negative ROE (-185.2%) and net margin (-405.1%)
- Dependence on non-recurring or milestone-type revenue to meet near-term targets
Key Takeaways:
- Business model remains R&D-centric with structurally negative operating leverage at current scale
- Liquidity ratios suggest near-term obligations are covered, but true cash position is undisclosed
- Low leverage in yen terms reduces immediate solvency risk, but funding dependence persists
- Revenue volatility is likely to continue given partnership/milestone dynamics
- Path to profitability requires substantial revenue step-up or material cost reprioritization
Metrics to Watch:
- Cash and equivalents balance and quarterly operating cash burn (once disclosed)
- New licensing deals, upfronts, and milestone receipts
- R&D expense trajectory and program prioritization decisions
- Clinical and regulatory milestones that can unlock partnership value
- Backlog or visibility on collaboration revenue
- Equity issuance or other financing activities and resulting dilution
Relative Positioning:
Within Japan-listed development-stage biopharma, Karuna BioScience exhibits a typical profile of high gross margin, low recurring revenue, and substantial R&D-driven losses, with relatively low balance sheet leverage but elevated funding reliance compared to diversified peers and commercial-stage companies.
This analysis was auto-generated by AI. Please note the following:
- No Guarantee of Accuracy: The accuracy and completeness of this analysis are not guaranteed. For accurate financial data, please refer to the original disclosure documents published on TDnet or other official sources
- Not Investment Advice: This analysis is for general informational purposes only and does not constitute investment advice under applicable securities laws. It is not a recommendation to buy or sell any specific securities
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