- Net Sales: ¥2.31B
- Operating Income: ¥-344M
- Net Income: ¥-340M
- EPS: ¥-24.29
| Item | Current | Prior | YoY % |
|---|
| Net Sales | ¥2.31B | ¥2.37B | -2.4% |
| Operating Income | ¥-344M | ¥-27M | -1174.1% |
| Non-operating Income | ¥23M | - | - |
| Non-operating Expenses | ¥227M | - | - |
| Ordinary Income | ¥-426M | ¥-231M | -84.4% |
| Income Tax Expense | ¥113M | - | - |
| Net Income | ¥-340M | - | - |
| Net Income Attributable to Owners | ¥-568M | ¥-339M | -67.6% |
| Total Comprehensive Income | ¥-583M | ¥-494M | -18.0% |
| Depreciation & Amortization | ¥145M | - | - |
| Interest Expense | ¥29M | - | - |
| Basic EPS | ¥-24.29 | ¥-15.71 | -54.6% |
| Dividend Per Share | ¥0.00 | ¥0.00 | - |
| Item | Current End | Prior End | Change |
|---|
| Current Assets | ¥4.54B | - | - |
| Cash and Deposits | ¥3.34B | - | - |
| Non-current Assets | ¥5.12B | - | - |
| Property, Plant & Equipment | ¥529M | - | - |
| Intangible Assets | ¥3.90B | - | - |
| Item | Current | Prior | Change |
|---|
| Operating Cash Flow | ¥229M | - | - |
| Financing Cash Flow | ¥3.05B | - | - |
| Item | Value |
|---|
| Net Profit Margin | -24.6% |
| Current Ratio | 382.2% |
| Quick Ratio | 382.2% |
| Debt-to-Equity Ratio | 0.68x |
| Interest Coverage Ratio | -11.82x |
| EBITDA Margin | -8.6% |
| Item | YoY Change |
|---|
| Net Sales YoY Change | -2.5% |
| Item | Value |
|---|
| Shares Outstanding (incl. Treasury) | 24.46M shares |
| Treasury Stock | 181 shares |
| Average Shares Outstanding | 23.43M shares |
| Book Value Per Share | ¥247.04 |
| EBITDA | ¥-199M |
| Item | Amount |
|---|
| Q2 Dividend | ¥0.00 |
| Year-End Dividend | ¥0.00 |
| Item | Forecast |
|---|
| Net Sales Forecast | ¥3.89B |
| Operating Income Forecast | ¥118M |
| Ordinary Income Forecast | ¥73M |
| Net Income Attributable to Owners Forecast | ¥-71M |
| Basic EPS Forecast | ¥-3.25 |
| Dividend Per Share Forecast | ¥0.00 |
This data was automatically extracted from XBRL files. Please refer to the original disclosure documents for accuracy.
RaQualia Pharma (4579) reported FY2025 Q3 consolidated results under JGAAP showing revenue of ¥2,311 million, down 2.5% YoY, reflecting the inherently lumpy nature of drug discovery licensing and milestone income. Operating loss was ¥344 million, essentially flat YoY, indicating disciplined operating cost control amid modest top-line softness. Ordinary loss widened to ¥426 million, with interest expenses of ¥29 million weighing on financial income. Net loss was ¥568 million (EPS: -¥24.29), also flat YoY, suggesting that cost and tax effects broadly offset revenue headwinds. The DuPont framework indicates a negative ROE of -9.40%, driven by a net margin of -24.58% and low asset turnover of 0.243, partially cushioned by moderate financial leverage of 1.58x. EBITDA was negative at -¥199 million, and the EBITDA margin stood at -8.6%, consistent with a research-led business model without recurring product gross profit. Liquidity appears solid with current assets of ¥4,539 million and current liabilities of ¥1,187 million, yielding a current ratio of 382%, and working capital of ¥3,351 million. Total assets were ¥9,518 million, equity ¥6,042 million, and total liabilities ¥4,085 million, implying liabilities-to-equity of 0.68x and an indicative equity ratio around the mid-60% range based on the provided balance sheet figures. Operating cash flow was positive at ¥229 million despite the net loss, supported by non-cash charges (D&A of ¥145 million) and likely working capital movements. Financing cash inflow of ¥3,048 million suggests recent capital raising or debt drawdown to bolster liquidity for pipeline progress. Interest coverage is negative given negative EBITDA and operating loss, underscoring dependence on external funding until monetization events scale. The reported zero values for cost of sales, gross profit, inventories, investing cash flow, equity ratio, cash balance, and share data appear to reflect non-disclosure or different account classifications rather than actual zeros; analysis is therefore based only on the available non-zero datapoints. Revenue resilience with only a small YoY decline and stable operating loss point to relatively steady execution of licensing activities. However, profitability remains sensitive to timing of milestones and partner payments, and cost discipline remains critical until scale improves. With no dividends (DPS: ¥0.00) and continued losses, internal reinvestment and balance sheet strength are the near-term priorities. Overall, the company retains ample liquidity and an equity-heavy capital structure, but sustained progress in out-licensing, milestones, or optioned programs is essential to improve margins, cash generation, and ROE.
ROE of -9.40% decomposes into a net margin of -24.58%, asset turnover of 0.243x, and financial leverage of 1.58x. The negative net margin reflects the absence of recurring product gross profit and reliance on milestone/licensing revenue, with operating expenses exceeding revenue in the quarter-to-date period. Asset turnover at 0.243x is low, typical for R&D-centric models where assets are largely cash, intangibles, and preclinical/clinical investments rather than inventory-backed operations. Financial leverage is modest; liabilities-to-equity of 0.68x provides some cushion but does not materially enhance ROE due to negative margins. EBITDA of -¥199 million and an EBITDA margin of -8.6% indicate limited operating leverage at current revenue levels; incremental revenue from milestones can swing margins quickly given a largely fixed cost base. Operating loss of ¥344 million is flat YoY, suggesting effective cost containment despite a slight revenue decline. Ordinary loss of ¥426 million includes ¥29 million interest expense, evidencing some financial burden even with a conservative leverage profile. Effective tax outflow of ¥113 million alongside a net loss likely reflects non-income taxes or tax adjustments rather than current tax on profits. Interest coverage is negative (metrics indicate -11.8x), meaning current operating earnings do not cover interest; continued reliance on equity financing or non-dilutive upfronts/milestones is important. Overall margin quality is event-driven; with each large contract or milestone, operating leverage can improve sharply, but absent such events, losses persist. The stability of the operating loss despite lower revenue implies some flexibility in spending cadence, but sustained profitability requires higher and more recurring revenue.
Revenue of ¥2,311 million declined 2.5% YoY, a relatively modest contraction for a licensing-driven model, implying some continuity in partner payments or service revenue. Profitability metrics remained broadly stable YoY at the operating and net levels, indicating that cost discipline helped offset top-line softness. Given the business model, revenue sustainability depends on milestone timing, option exercises, and potential new out-licensing; quarter-to-quarter volatility is expected. The positive operating cash flow despite a net loss suggests that non-cash expenses and working capital management are supporting near-term cash conversion, but structural growth hinges on pipeline monetization. With financing cash inflows of ¥3,048 million, the company appears to have extended its runway to progress programs toward value-inflecting events. Depreciation of ¥145 million implies a tangible/intangible asset base that will continue to generate non-cash charges, supporting OCF if revenue normalizes. Outlook: if additional milestones are recognized or new agreements are signed, operating leverage could turn margins positive; absent such events, growth may remain muted and losses persist. The slight YoY decline does not point to a demand problem per se, but rather timing effects; monitoring contract backlog and milestone schedules will be key. Overall growth quality remains tied to external partnerships and regulatory/clinical progress, which are binary and timing-sensitive.
Liquidity is strong: current assets of ¥4,538,963 thousand against current liabilities of ¥1,187,495 thousand yield a current ratio of 382% and working capital of ¥3,351,468 thousand. Quick ratio matches the current ratio because inventories were not disclosed (reported as zero), suggesting a cash-and-receivables-heavy current asset mix typical of R&D entities. Total assets are ¥9,518 million and total equity ¥6,042 million; this implies an indicative equity ratio of approximately 63–64% and a liabilities-to-equity ratio of 0.68x, reflecting a conservative balance sheet. Interest expense is ¥29 million, and with negative operating earnings, interest coverage is negative; however, the absolute interest burden is modest relative to equity and total assets. Financing cash inflow of ¥3,048 million meaningfully strengthened the balance sheet in the period, likely through equity issuance or new borrowing; share data is undisclosed, so dilution cannot be quantified here. No cash and equivalents balance was reported (zero), which should be treated as undisclosed; nonetheless, the strong current ratio and positive OCF imply adequate near-term liquidity. Solvency is supported by the sizable equity base and moderate leverage, but sustained losses could erode equity over time if not offset by financing or improved revenue.
Operating cash flow was positive at ¥229,303 thousand despite a net loss of ¥568,000 thousand, yielding an OCF/Net Income ratio of -0.40 (positive OCF over negative NI), which suggests supportive non-cash items and/or favorable working capital. D&A of ¥144,670 thousand is a key driver of non-cash add-backs and will continue to support OCF if capex remains contained. Free cash flow is not determinable from the disclosed data because investing cash flows were not reported (shown as zero); thus, FCF listed as zero should be treated as undisclosed, not actual zero. Working capital increased on a net basis given the strong current asset position versus current liabilities, supporting liquidity. Interest outflows of ¥29,112 thousand are manageable in size, though not covered by operating profit; they are covered by OCF in the period. The positive OCF in the face of operating losses suggests that earnings quality, from a cash conversion standpoint, is reasonable for a milestone-driven model, but recurring cash generation remains unproven without consistent revenue. Financing inflows of ¥3,048,283 thousand reduced reliance on internal cash generation in the period.
The company paid no dividend (DPS: ¥0.00) and recorded losses (EPS: -¥24.29), implying a payout ratio of 0%. With negative net income and undetermined free cash flow (investing CF undisclosed), there is no basis for dividend initiation in the near term from an earnings coverage perspective. Even though OCF was positive, sustainable FCF coverage cannot be assessed without capex data; prudence suggests retained earnings and cash should fund R&D and partnering activities. Given the financing inflow of ¥3,048 million and the strategic focus on R&D, a no-dividend policy remains consistent with capital allocation priorities. Future dividend capacity would hinge on achieving sustained profitability and positive, recurring FCF from licensing streams or product royalties.
Business Risks:
- Revenue volatility due to milestone and licensing timing
- Dependence on external partners for development, option exercises, and payments
- Clinical and regulatory binary risk inherent in drug discovery programs
- Potential delays in R&D timelines affecting cash receipts
- Concentration risk if a small number of agreements drive the majority of revenue
Financial Risks:
- Negative operating earnings leading to ongoing reliance on external financing
- Negative interest coverage; exposure to higher interest costs if leverage increases
- Equity dilution risk given recent ¥3.0 billion financing inflow
- Potential erosion of equity if losses persist
- Uncertainty around cash balance and capex due to undisclosed items
Key Concerns:
- Sustained negative ROE (-9.40%) driven by weak margins and low asset turnover
- Event-driven revenue model with limited visibility
- Limited disclosure on cash, investing activities, and share count complicates runway analysis
Key Takeaways:
- Revenue modestly declined 2.5% YoY to ¥2,311 million, while operating loss remained flat at ¥344 million, signaling cost control.
- ROE is negative at -9.40%, with net margin of -24.58% and low asset turnover of 0.243x.
- Liquidity is strong: current ratio 382% and working capital ¥3.35 billion.
- Operating cash flow positive at ¥229 million despite losses, supported by ¥145 million D&A.
- Financing inflow of ¥3.05 billion extends runway but may imply dilution; share details undisclosed.
- Interest coverage negative; profitability inflection requires larger or more frequent milestones.
Metrics to Watch:
- New out-licensing deals and milestone schedules (timing and size)
- Operating expense trajectory versus revenue realization
- Operating cash flow and any disclosed capex to infer true FCF
- Equity and cash balances once disclosed; runway length
- Ordinary income trend and interest burden relative to OCF
Relative Positioning:
Among domestic drug discovery peers, the company exhibits a typical profile of negative operating earnings, event-driven revenue, and strong liquidity bolstered by financing; positive OCF in the period is a relative strength, but sustained profitability remains contingent on incremental milestone/royalty scale.
This analysis was auto-generated by AI. Please note the following:
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