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DELCATH SYSTEMS, INC. (DCTH) stock intrinsic value fair value estimate & owner earnings analysis

Margin of safety$3.00 ComplexityAverage Updated
$2.16 $9.74
bear $2.16 base $5.75 bull $9.74 margin of safety $3.00 market price* $14.08
Delcath makes HEPZATO KIT, a system that isolates the liver's blood supply so a high dose of the chemotherapy drug melphalan can be pumped straight into liver tumours and filtered out before it reaches the rest of the body. The FDA approved it in August 2023 for liver-dominant metastatic uveal melanoma, a rare eye cancer that spreads to the liver; a European version, CHEMOSAT, has been sold for longer. HEPZATO is the only approved treatment for the roughly 55% of these patients who cannot receive Immunocore's KIMMTRAK. Revenue went from $2.1 million in 2023 to $37.2 million in 2024 and $85.2 million in 2025 ($78.8 million HEPZATO, $6.4 million CHEMOSAT), with 24 US centers treating patients in 2025 against 14 a year earlier. The first half of 2026 brought $54.1 million of revenue, up 23%, and the second quarter alone was $29.1 million. What the business earns for owners. We start from operating cash flow, strip out the timing effect of working capital, and charge stock compensation as the real cost it is, because Delcath pays a large part of its staff in shares. In 2025 the business generated $25.6 million of cash before working-capital swings, but stock compensation was $24.2 million, and maintenance spending on equipment was about $0.6 million. That leaves owner earnings of about $0.8 million, or 2 cents a share: the first positive year in the company's history, after losses of $35 million in 2022, $39 million in 2023 and $13 million in 2024. Every earlier year described a company that was still trying to get approved, so it tells us nothing about the earning power of today's business. That leaves one barely positive year and two quarters, which is far too little to set a normal earnings level with any confidence. Our previous figures understated 2025 slightly because they did not separate out working-capital movements; the business has not changed for that reason. How we built the cases. We credit only revenue the company has already reached. No further growth is assumed in any case, because expansion to more centers, more patients per center and new indications have not happened yet. The second-quarter 2026 revenue rate of about $116 million a year is the starting level. Gross margin runs about 86-88%. The big swing item is the cost structure: selling and administration of about $52 million and research of about $29 million in 2025, now rising as the company runs Phase 2 trials in colorectal and breast cancer liver metastases. We treat those trials as optional spending that ends once they read out, not as a source of value, since no result exists yet. Delcath has about $101 million of usable federal tax losses (another $195 million will expire unused because of past ownership changes), so it pays little federal tax for several years. Orphan exclusivity for the uveal melanoma indication runs seven years from the 2023 approval, to about 2030, and the device is protected by 13 US utility patents plus trade secrets in manufacturing the filter and catheter. Base case: revenue holds at about $116 million and costs stay near today's level while the trials run through 2028, so the business throws off only $5-7 million a year after stock compensation. Once the trial spending ends, research falls back toward $22 million and owner earnings settle around $24 million a year. Exclusivity lapses around 2030, and IDEAYA's darovasertib combination and Replimune's RP2 are already in registration-stage trials in the same disease. On that evidence we assume the franchise holds through about 2036 and then fades to nothing by 2040 instead of running forever, because nothing proven yet replaces it. The business is worth about $143 million. Delcath has no debt and held $95.9 million of cash and short-term investments at June 30, 2026. Setting aside about $10 million for day-to-day needs, the shares are worth about $229 million, or $5.75 each on 39.8 million diluted shares. The diluted count includes the Series E and F convertible preferred, which convert into common stock at $3.30-$10.00 a share. Bear case: this is a one-product, one-indication business with a hospital customer base and a competitor pipeline, and that is the risk we model. Revenue holds near $110 million through 2028 while trial spending absorbs almost all the cash. In 2030 orphan exclusivity ends and a newly approved drug from the current pipeline takes share, so revenue falls toward $72 million, the business runs at a small loss after stock compensation, and we assume management cuts the business back by 2033 rather than burning the cash. The operating business is worth roughly nothing, and the shares are worth roughly the cash, about $2.16. The case does not include a product recall or a safety-driven label change. These have not happened, but they are the outcomes most likely to be worse than this case. Bull case: centers already treating patients keep growing usage as they did in 2025, revenue reaches about $150 million by 2028, and once trial spending ends owner earnings reach about $47 million a year and fade from 2036 to 2042. The business is worth about $302 million, or $9.74 a share with the cash. A positive colorectal or breast cancer trial would add value beyond this, but that is not in hand and is not counted. Margin-of-safety price. We are not confident in the earnings level. There is one barely positive year, stock compensation is as large as operating cash flow, and the whole business depends on one product in one rare cancer, sold to a few dozen hospitals; one customer was 15% of 2025 revenue. If the next registration-stage drug in uveal melanoma succeeds around 2029-2030, much of this business could go away. The balance sheet provides protection: no debt and about $2.40 a share of cash and investments, partly shrunk by a $25 million buyback authorised in November 2025. If we are wrong about cost discipline or about competition, the shares are worth about the cash. If we are wrong in the other direction, they are worth $8-10. The price assumes a three-to-four-year holding period, through the trial readouts and the 2030 exclusivity date, with no dividend while waiting. At $3.00 the price is about 60 cents a share beyond the cash for a business already selling at a $116 million annual rate. If the base case plays out, from $3.00 it implies about 20% a year toward $5.75 over roughly 3.5 years, and the bear case implies a decline of about 28% if the business proves worth only its cash. That is the highest price at which we think the odds support a 20% return.
Fiscal yearOwner's earningsMethodology
2025 $0.02 ▼
RECOMPUTED on current basis (prior row omitted the working-capital adjustment and deducted total rather than maintenance capex). OE = CFO - dWC - SBC - maintenance capex. CFO=$22,516K; dWC (cash-flow lines: prepaids -3,421, receivables -854, inventory -3,319, payables/accrued +4,766, other non-current liabilities -241) = $(3,069)K, so CFO ex-WC = $25,585K; SBC=$24,232K; capex=$1,547K, capex/revenue ratio (2023-2025 mean) 2.04% x revenue growth $48,026K = growth capex $981K, maintenance capex=$566K; OE = 25,585 - 24,232 - 566 = $787K; diluted shares=39,919,557; OE/sh=$0.0197. Reconciliation: NI 2,700 + SBC 24,232 + depreciation 238 + ROU amort 111 - marketable-securities accretion 1,696 = 25,585 ex-WC, matches exactly. Source: FY2025 10-K, accession 0001628280-26-012019.
2024 -$0.45 ▼
RECOMPUTED on current basis (prior row omitted the working-capital adjustment and deducted total capex). OE = CFO - dWC - SBC - maintenance capex. CFO=$(18,681)K; dWC (prepaids -1,639, receivables -10,649, inventory -3,611, payables/accrued +479, other non-current -101) = $(15,521)K, so CFO ex-WC = $(3,160)K; SBC=$9,767K; capex=$559K, growth capex = 2.04% x revenue growth $35,140K = $718K (exceeds capex) so maintenance capex=$0; OE=$(12,927)K; diluted shares=28,511,393; OE/sh=$(0.4534). Reconciliation: NI (26,386) + SBC 9,767 + depreciation 134 + warrant fair-value loss 14,071 + ROU 95 + debt discount 460 + accrued note interest 133 - note interest paid 847 - securities accretion 587 = (3,160), exact. First commercial year of HEPZATO KIT. Source: FY2025 10-K comparative column, accession 0001628280-26-012019.
2023 -$2.38 ▼
RECOMPUTED on current basis (prior row omitted the working-capital adjustment). OE = CFO - dWC - SBC - maintenance capex. CFO=$(31,251)K; dWC (prepaids +1,029, receivables +125, inventory -1,324, payables/accrued -199, other non-current -537, deferred revenue 0) = $(906)K, so CFO ex-WC = $(30,345)K; SBC=$8,151K; capex=$58K, revenue declined (2,065 vs 2,719) so growth capex=$0, maintenance capex=$58K; OE=$(38,554)K; diluted shares=16,229,931; OE/sh=$(2.3755). Reconciliation: NI (47,678) + SBC 8,151 + depreciation 128 + warrant fair-value loss 7,998 + lease 271 + debt discount 776 + accrued note interest 160 - securities accretion 151 = (30,345), exact. HEPZATO KIT FDA approval year. Source: FY2023 10-K, accession 0001628280-24-013008.
2022 -$3.97 ▼
RECOMPUTED on current basis (prior row omitted the working-capital adjustment). OE = CFO - dWC - SBC - maintenance capex. CFO=$(24,950)K; dWC (prepaids +774, receivables -322, inventory -587, payables/accrued +1,798, other non-current +621, deferred revenue -170) = +$2,114K, so CFO ex-WC = $(27,064)K; SBC=$7,941K; capex=$209K, revenue declined (2,719 vs 3,555) so maintenance capex=$209K; OE=$(35,214)K; diluted shares=8,864,615; OE/sh=$(3.9724). Reconciliation: NI (36,508) + SBC 7,941 + depreciation 132 + lease 443 + debt discount 768 + accrued note interest 160 = (27,064), exact. Source: FY2023 10-K comparative column, accession 0001628280-24-013008 (agrees with FY2022 10-K 0001193125-23-079836).
2021 -$3.45 ▼
RECOMPUTED: prior row omitted SBC (untagged) and the working-capital adjustment and used period-end shares; SBC and weighted diluted shares are now taken from the FY2022 10-K cash-flow statement. OE = CFO - dWC - SBC - maintenance capex. CFO=$(22,604)K; dWC (prepaids +813, receivables +13, inventory -557, payables/accrued -3,284, other liabilities -322, deferred revenue -2,427) = $(5,764)K, so CFO ex-WC = $(16,840)K; SBC (stock option compensation) = $7,832K; capex=$143K, growth capex = 19.6% (2020-22 mean capex/revenue) x revenue growth $1,899K = $373K, exceeds capex, so maintenance capex=$0; OE=$(24,672)K; weighted diluted shares=7,145,754; OE/sh=$(3.4527). Reconciliation: NI (25,649) + SBC 7,832 + depreciation 146 + ROU 322 + debt discount 323 + accrued note interest 186 = (16,840), exact. Revenue 2021 includes $1.7M one-time recognition of deferred license revenue. Source: FY2022 10-K, accession 0001193125-23-079836 (comparative column) and FY2021 10-K 0001193125-22-090104.
2020 -$7.51 ▼
OE = CFO - dWC - SBC - maintenance capex. CFO=$(22,868)K; dWC (prepaids -910, receivables -36, inventory -201, payables/accrued -4,396, deferred revenue -263) = $(5,806)K, so CFO ex-WC = $(17,062)K; SBC = stock options 3,505 + restricted stock 406 = $3,911K; capex=$782K, revenue 1,656 (no prior-year comparable used; treated as no growth) so maintenance capex=$782K; OE=$(21,755)K; weighted diluted shares=2,897,827 (after 1:700 reverse split of Dec 2019); OE/sh=$(7.5073). Reconciliation: NI (24,156) + SBC 3,911 + depreciation 167 + ROU 25 + warrant fair-value loss 2,832 - non-cash interest 1 + accrued note interest 160 = (17,062), exact. Pre-approval, pre-commercial company. Source: FY2020 10-K, accession 0001564590-21-016962.
2019 -$711.51 ▼
OE = CFO - dWC - SBC - maintenance capex. CFO=$(23,689)K; dWC (prepaids -807, receivables +497, inventory +204, payables/accrued -4,350, deferred revenue -479, other liabilities -627) = $(5,562)K, so CFO ex-WC = $(18,127)K; SBC = options 273 + restricted 4 = $277K; capex=$24K, maintenance capex=$24K; OE=$(18,428)K; weighted diluted shares=25,900 (restated for 1:700 reverse split effected 24 Dec 2019; per-share figure is extreme because of near-total dilution since); OE/sh=$(711.51). Reconciliation: NI (8,879) + SBC 277 + depreciation 212 + ROU 37 + warrant fair-value gain (17,493) - non-cash interest 11 + equitization of expenses 1,474 + loss on financial instruments 1,715 + accrued note interest 74 + debt discount 4,467 = (18,127), exact. Source: FY2020 10-K comparative column, accession 0001564590-21-016962.

Owner's earnings per share by fiscal year, most recent first. Tap a row to see how that figure was calculated, including the source filing.

Sales geography
United States (about 92% of 2025 revenue, from HEPZATO KIT sold to hospitals and cancer treatment centers nationwide); Europe (about 8%, CHEMOSAT sold through European hospitals, distributed from Galway, Ireland).
Historical growth strategy
Single-platform development company that spent two decades and repeated equity raises (five reverse splits since its 2000 IPO) to win FDA approval of its liver-perfusion system, then grew by activating more US treatment centers (14 in 2024, 24 in 2025) for its one approved indication; now funding Phase 2 trials to extend the same device into colorectal and breast cancer liver metastases rather than acquiring products.
Chart analysis
A chartist would describe a long history of collapse followed by a base and breakout: decades of decline and repeated reverse splits, then a strong multi-year uptrend after the 2023 FDA approval and 2024 commercial launch, with the stock trading well above its 2023 lows. More recently momentum has stalled, with the shares pulling back from their highs into a choppy range. A trend follower would want to see the shares reclaim prior highs on rising volume before calling the uptrend intact, and would treat a break below the recent range lows as confirmation of a deeper correction.
Competitors

Companies we consider competitors of DCTH. Tap a ticker to open our analysis of that company in a new tab.

Circle of competence

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