$IMTX earnings report

Immatics reports Q3 2026 net loss of €(76,022) thousand as R&D expense rises on SUPRAME Phase 3 activity. AlphAI read Immatics's Q3 2026 and nine months 2026 filing as mixed. 2 quarters are on record below.

Q3 2026 and nine months 2026

AlphAI · Earnings readIMTX · Q3 2026 and nine months 2026 · ended 2026-09-30

Immatics reports Q3 2026 net loss of €(76,022) thousand as R&D expense rises on SUPRAME Phase 3 activity

→Mixed quarter

Quarterly collaboration revenue rose to €6,923 thousand and the company completed a financing, but the net loss widened to €(76,022) thousand from €(50,545) thousand, R&D expense rose to €(70,270) thousand, and nine-month collaboration revenue fell to €23,679 thousand after the BMS agreement ended. The filing reports no guidance figures.

Revenue
€6.92M
increased by €1.7 million y/y
Moderna collaboration revenue, Q3 2026
€6.92M
EPS · other
(0.50)

Key metrics

shortened, hover for the filing’s print
MetricValueq/qy/y
Revenue from collaboration agreements, Q3 2026other€6.92M–increased by €1.7 million
Revenue from collaboration agreements, nine months 2026other€23.68M–decreased by €4.8 million
Research and development expenses, Q3 2026other−€70.27M––
Research and development expenses, nine months 2026other−€191.9M––
General and administrative expenses, Q3 2026other−€15.81M––
General and administrative expenses, nine months 2026other−€44.26M––
Other income, Q3 2026other€615K––
Other income, nine months 2026other€639K––
Operating result, Q3 2026other−€78.54M––
Operating result, nine months 2026other−€211.8M––
Change in liabilities for warrants, Q3 2026other−€3.26M––
Change in liabilities for warrants, nine months 2026other−€3.26M––
Other financial income, Q3 2026other€5.82M––
Other financial income, nine months 2026other€18.97M––
Other financial expenses, Q3 2026other−€440K––
Other financial expenses, nine months 2026other−€858K––
Financial result, Q3 2026other€2.11M––
Financial result, nine months 2026other€14.85M––
Loss before taxes, Q3 2026other−€76.43M––
Loss before taxes, nine months 2026other−€197.0M––
Taxes on income (benefit), Q3 2026other€407K––
Taxes on income (benefit), nine months 2026other€629K––
Net loss, Q3 2026other−€76.02M––
Net loss, nine months 2026other−€196.3M––
Net loss per share, basic and diluted, Q3 2026other(0.50)––
Net loss per share, basic and diluted, nine months 2026other(1.39)––
Net cash used in operating activities, nine months 2026other−€163.2M––
Net cash used in investing activities, nine months 2026other−€70.90M––
Net cash provided by financing activities, nine months 2026other€158.2M––

Segments

SegmentRevenueq/qy/y
Moderna collaboration revenue, Q3 2026Prior-year Q3 2025 figure printed as €4,231 thousand. Company attributes the increase to a received milestone payment of €1.1 million and a higher proportion of costs incurred relative to the overall project budget within the quarter.€6.92M––
Moderna collaboration revenue, nine months 2026Prior-year nine-month figure printed as €22,428 thousand. Company attributes the decrease to a lower proportion of costs incurred relative to the overall project budget, partially offset by received milestone payments of €1.6 million.€20.84M––
BMS collaboration revenue, Q3 2026Prior-year Q3 2025 figure printed as €956 thousand. The BMS collaboration agreement ended in August 2026, and the remaining deferred revenue was recognized in the second quarter of 2026.nil (dash in filing)––
BMS collaboration revenue, nine months 2026Prior-year nine-month figure printed as €6,077 thousand. Company states the BMS agreement ended in August 2026 and remaining deferred revenue was fully recognized during the nine months.€2.84M––

Capital returns

  • No share repurchases or dividends are reported in the filing.
  • On August 26, 2026 the company closed an offering of 15,535,100 ordinary shares at €7.45 ($8.69) per share, with gross proceeds of €115.7 million ($135.0 million) less transaction costs of €7.3 million ($8.5 million).
  • On August 26, 2026 the company issued 4,315,304 pre-funded warrants at €7.446 ($8.689) per warrant share, with gross proceeds of €32.1 million ($37.5 million) less transaction costs of €2.0 million ($2.2 million).
  • On March 12, 2026 the company issued 2,500,000 ordinary shares under its ATM program with Leerink Partners LLC at €8.68 ($10.02) per share, for gross proceeds of €21.6 million ($25.0 million) less transaction costs of €0.5 million ($0.6 million).
  • There were no ATM sales during the three months ended September 30, 2026.

What drove it

  • Company explanation for TCR T-cell therapy direct external R&D increase: increased activities in clinical trials for anzu-cel (IMA203), predominantly for SUPRAME. Q3 2026 was €30,026 thousand versus €13,971 thousand in Q3 2025.
  • Company explanation for TCR bispecific direct external R&D increase: increased clinical trial activities related to development of IMA402. Q3 2026 was €7,333 thousand versus €5,970 thousand in Q3 2025.
  • Company explanation for personnel-related R&D increase: headcount growth from increased R&D activity, particularly clinical trials. Q3 2026 was €21,811 thousand versus €16,628 thousand in Q3 2025.
  • Company explanation for G&A increase: increased engagement in commercialization preparation activities for anzu-cel (IMA203), affecting personnel-related and professional and consulting fees.
  • Company explanation for other financial income increase in Q3 2026: higher foreign exchange gains, partially offset by lower interest income due to lower interest rates and lower balances of cash and cash equivalents and other financial assets.
  • Company explanation for lower nine-month other financial expenses: lower foreign exchange losses. Nine-month 2025 was €(36,151) thousand.
  • Change in liabilities for warrants in Q3 2026 of €(3,263) thousand includes a €1.3 million increase in the value of pre-funded warrant liabilities and €2.0 million of underwriting discount fully amortized, per the filing.
  • Company states the BMS collaboration agreement ended in August 2026 and remaining deferred revenue was recognized in Q2 2026.
  • Headcount was 721 full-time equivalent employees as of September 30, 2026, compared with 656 as of December 31, 2025, per the MD&A.

Concerns

  • Net loss widened to €(76,022) thousand in Q3 2026 from €(50,545) thousand in Q3 2025, and nine-month net loss was €(196,328) thousand versus €(160,749) thousand.
  • Operating result for nine months 2026 was €(211,809) thousand versus €(143,135) thousand in nine months 2025.
  • Nine-month collaboration revenue fell to €23,679 thousand from €28,505 thousand as the BMS agreement ended in August 2026.
  • Net cash used in operating activities rose to €(163,204) thousand for nine months 2026 from €(117,961) thousand.
  • Accumulated deficit reached €(982,316) thousand as of September 30, 2026.
  • Total shareholders' equity declined to €438,499 thousand from €484,099 thousand at December 31, 2025, despite equity raises.
  • Liabilities for warrants of €33,363 thousand are newly recognized and are measured at amortized cost, with the company noting judgments on pre-funded warrant classification and earnings per share calculation.
  • Accounts payables increased to €40,275 thousand from €18,832 thousand, including accrued liabilities of €31,087 thousand.

What to watch

  • SUPRAME Phase 3: the company states enrollment is on track to complete required randomizations by year-end 2026 to support the final primary endpoint analysis.
  • Company expects to disclose topline data from the final PFS analysis of SUPRAME in the first half of 2027, followed by a BLA submission in 2027.
  • Revenue from the Moderna collaboration, which is recognized over time on a cost-to-cost basis and includes remaining deferred revenue of €22,035 thousand in total.
  • Liabilities for warrants: changes in the valuation of pre-funded warrants flow through the statement of loss as change in liabilities for warrants.
  • IFRS 18 adoption from January 1, 2027 with restated presentation of the statement of loss and cash flow categories, per the filing.
  • Cash runway: company cites sufficiency through at least 12 months and holds €472.3 million in cash, cash equivalents and other financial assets.

Balance sheet and cash flow

  • Cash and cash equivalents: €276,614 thousand as of September 30, 2026, compared with €345,918 thousand as of December 31, 2025.
  • Cash, cash equivalents and other financial assets: €472.3 million as of September 30, 2026, per the MD&A.
  • Other financial assets (short-term deposits): €195,655 thousand as of September 30, 2026, compared with €123,419 thousand as of December 31, 2025.
  • Total assets: €565,723 thousand as of September 30, 2026, compared with €562,337 thousand as of December 31, 2025.
  • Total shareholders' equity: €438,499 thousand as of September 30, 2026, compared with €484,099 thousand as of December 31, 2025.
  • Liabilities for warrants: €33,363 thousand as of September 30, 2026, compared with nil as of December 31, 2025.
  • Accounts payables: €40,275 thousand as of September 30, 2026, compared with €18,832 thousand as of December 31, 2025.
  • Accumulated deficit: €(982,316) thousand as of September 30, 2026, compared with €(785,988) thousand as of December 31, 2025.
  • Deferred revenue (current plus non-current): €22,035 thousand as of September 30, 2026, compared with €34,357 thousand as of December 31, 2025.
  • Net cash used in operating activities for nine months 2026 is €163.2 million; the company cites a loss before tax of €197.0 million, offset by non-cash share-based compensation of €16.9 million and a working capital increase of €13.2 million.
  • Company states it believes existing cash, cash equivalents and other financial assets are sufficient to fund operations through at least the next 12 months, and the statements are prepared on a going concern basis.

Analysis

Immatics reported a net loss of €(76,022) thousand for the third quarter of 2026, against €(50,545) thousand a year earlier, and €(196,328) thousand for the nine months against €(160,749) thousand. The loss was driven by operating costs rather than by financial items. R&D expense for the quarter was €(70,270) thousand against €(47,176) thousand, with direct external TCR T-cell therapy spending rising to €30,026 thousand from €13,971 thousand. The company attributes this to clinical activity for anzu-cel (IMA203), predominantly SUPRAME. G&A rose to €(15,810) thousand from €(12,673) thousand, which the company links to commercialization preparation for anzu-cel.

Collaboration revenue moved in the opposite direction over the nine months. Revenue was €23,679 thousand against €28,505 thousand, following the end of the BMS agreement in August 2026. Quarterly revenue of €6,923 thousand was higher than the €5,187 thousand of Q3 2025, which the company explains by a €1.1 million milestone payment and a higher proportion of costs incurred relative to the project budget. Moderna remains the only revenue-generating collaboration as of September 30, 2026, and nine-month Moderna revenue fell to €20,836 thousand from €22,428 thousand.

Below the operating line, the financial result turned positive for the quarter at €2,113 thousand, against €3,961 thousand a year earlier, with other financial income of €5,816 thousand and a change in liabilities for warrants of €(3,263) thousand. The company explains the higher other financial income by foreign exchange gains, partly offset by lower interest income. Nine-month other financial expenses fell to €(858) thousand from €(36,151) thousand, which the company attributes to lower foreign exchange losses.

Capital allocation in the period was funded externally. The company closed an offering of 15,535,100 ordinary shares and issued 4,315,304 pre-funded warrants on August 26, 2026, and it issued 2,500,000 shares under its ATM program in March 2026. Net cash from financing was €158,196 thousand for nine months, while operating cash outflow was €(163,204) thousand. Cash and cash equivalents fell to €276,614 thousand from €345,918 thousand at year-end 2025. Including other financial assets of €195,655 thousand, the company reports €472.3 million in liquidity and states this is sufficient for at least 12 months. The filing contains no guidance figures, so no comparison to prior outlook is possible.

The figures that deserve attention are the widening operating loss, the €33,363 thousand liability for warrants recognized on the pre-funded warrants, and the trajectory of R&D headcount and clinical spend ahead of SUPRAME topline data expected in the first half of 2027.

Not in the filing

stated, not guessed
  • No guidance, outlook or forward-looking financial targets are provided in the filing; guidance field is null.
  • No prior-quarter (Q2 2026) income statement columns are printed, so prior_quarter and qoq_change fields are null.
  • Prior-year percentage changes for most income statement lines are not printed; yoy_change fields are null unless the MD&A states the change in euro amounts.
  • Prior-year comparison for cash and cash equivalents and total assets is the December 31, 2025 balance rather than a prior-year period; prior_year fields for these balance sheet items are null.
  • No executive quotes are included in the document.
  • No gross margin, cost of sales or non-GAAP measures are reported.
  • Operating cash flow prior-period comparison exists but no percentage change is printed.
  • Share price reaction, consensus estimates and analyst expectations are not provided in the document.

Written by an AI language model from the company’s SEC earnings filing (Form 8-K Item 2.02, or Form 6-K for a foreign private issuer). Every figure is checked against the filing text, and a metric the filing does not print, or whose value, prior period and change do not add up, is dropped from the metrics. The model can still misread a table, in the metrics or in the text, so check a number in the filing before you rely on it. Consensus estimates, price targets and share-price reactions are not shown because they are not in the filing. AI-generated research, not investment advice.

H1 2026

AlphAI · Earnings readIMTX · H1 2026 · ended June 30, 2026

H1 2026 collaboration revenue declined to €16,756 thousand while research and development expense rose to €121,597 thousand, resulting in a net loss of €120,306 thousand; cash, cash equivalents and other financial assets were €393.4 million.

→Mixed half-year

Second-quarter collaboration revenue increased versus the prior-year quarter and financial-result volatility eased sharply, but H1 collaboration revenue declined while clinical-development spending, operating cash use and the net loss increased. The company funded the period with an ATM issuance and stated that its existing capital resources are sufficient for at least the next 12 months.

Revenue
€16.8M
Moderna, United States
€13.9M
EPS · other
€(0.89)

Key metrics

shortened, hover for the filing’s print
MetricValueq/qy/y
Revenue from collaboration agreementsother€16.76M––
Revenue from collaboration agreements, three months ended June 30other€9.14M––
Moderna collaboration revenueother€13.91M––
BMS collaboration revenueother€2.84M––
Research and development expensesother−€121.6M––
Direct external research and development expenses, TCR T-cell therapy Programsother−€47.93M––
Direct external research and development expenses, TCR Bispecific Programsother−€8.24M––
Direct external research and development expenses, Other programsother−€1.14M––
Personnel-related research and development expenses excluding share-based compensationother−€41.24M––
Research and development share-based compensation expensesother−€6.19M––
Facility and depreciation research and development expensesother−€7.39M––
General and administrative expensesother−€28.45M––
Operating resultother−€133.3M––
Other financial incomeother€13.34M––
Other financial expensesother−€602K––
Financial resultother€12.74M––
Loss before taxesother−€120.5M––
Taxes on incomeother€222K––
Net lossother−€120.3M––
Net loss, three months ended June 30other−€62.49M––
Basic loss per shareother€(0.89)––
Diluted loss per shareother€(0.89)––
Basic loss per share, three months ended June 30other€(0.46)––
Diluted loss per share, three months ended June 30other€(0.46)––
FTEsother704––

Segments

SegmentRevenueq/qy/y
Moderna, United StatesRevenue decreased because of a lower proportion of costs incurred relative to the overall project budget during the six months ended June 30, 2026.€13.91M––
BMS, United StatesRevenue decreased because of a lower proportion of costs incurred relative to the overall project budget during the six months ended June 30, 2026.€2.84M––

Forward-looking disclosures as of August 18, 2026 outlook

  • NoteEnrollment in SUPRAME remains on track to complete required randomizations by year-end.
  • NoteThe Company expects to disclose topline data from the final PFS analysis in the first half of 2027, followed by a BLA submission in 2027.
  • NoteExisting Cash, cash equivalents and Other financial assets will be sufficient to fund operating expenses and capital expenditure requirements through at least the next 12 months.
  • NoteThe Company intends to increase the statistical power for the secondary endpoint of OS by enrolling approximately 90 additional patients, bringing the total trial size to approximately 450 patients.

What drove it

  • Second-quarter collaboration revenue increased to €9,144 thousand from €4,737 thousand. Moderna revenue was €6,488 thousand and BMS revenue was €2,656 thousand during the three months ended June 30, 2026.
  • The company received a €0.5 million Moderna milestone during the three and six months ended June 30, 2026.
  • The increase in TCR T-cell therapy direct external expense was primarily driven by increased anzu-cel clinical-trial activities, predominantly SUPRAME and to a lesser extent uveal melanoma.
  • The increase in TCR Bispecific Programs expense was driven by continued clinical-trial activities for IMA402 and IMA401.
  • Personnel-related R&D costs increased with headcount growth supporting research and development activities, particularly clinical trials.
  • General and administrative personnel costs and professional and consulting fees increased primarily with commercialization-preparation activities for anzu-cel.
  • Other financial income increased principally from higher foreign-exchange gains, partly offset by lower interest income resulting from lower interest rates and lower cash, cash equivalents and other financial-asset balances.
  • Other financial expenses decreased primarily because of lower foreign-exchange losses.

Concerns

  • H1 collaboration revenue was €16,756 thousand versus €23,318 thousand in the prior-year period, and the company has not generated revenue from sales of pharmaceutical products.
  • The net loss was €(120,306) thousand and net cash used in operating activities was €(102,504) thousand for H1 2026.
  • SUPRAME PFS events are occurring more slowly than originally modeled. The company intends to replace previously planned interim and final PFS analyses with a single final analysis based on a lower prespecified number of PFS events.
  • The company does not have any products approved for sale and states that additional financing may be needed to achieve its business objectives.
  • The company issued 2,500,000 ordinary shares under its ATM program during H1 2026.

What to watch

  • Completion of required SUPRAME randomizations by year-end.
  • Topline data from the SUPRAME final PFS analysis expected in the first half of 2027.
  • The planned BLA submission for anzu-cel in 2027.
  • The protocol amendments to increase SUPRAME enrollment by approximately 90 patients to approximately 450 patients.
  • Recognition of deferred revenue, which was €23,199 thousand as of June 30, 2026.
  • Future Moderna milestone recognition following the first patient dosed in Moderna's clinical trial in July 2026.

Balance sheet and cash flow

  • Cash and cash equivalents were €232,459 thousand as of June 30, 2026, compared with €345,918 thousand as of December 31, 2025.
  • Other financial assets were €160,891 thousand as of June 30, 2026, compared with €123,419 thousand as of December 31, 2025.
  • Cash, cash equivalents and other financial assets were €393.4 million as of June 30, 2026.
  • Net cash used in operating activities was €(102,504) thousand for the six months ended June 30, 2026, compared with €(73,261) thousand for the six months ended June 30, 2025.
  • Net cash used in investing activities was €(36,237) thousand for the six months ended June 30, 2026, compared with net cash provided by investing activities of €111,056 thousand for the six months ended June 30, 2025.
  • Net cash provided by financing activities was €20,305 thousand for the six months ended June 30, 2026, compared with €(1,464) thousand for the six months ended June 30, 2025.
  • The Group issued 2,500,000 ordinary shares on March 12, 2026 at €8.68 ($10.02) per ordinary share, receiving gross proceeds of €21.6 million ($25.0 million) less transaction costs of €0.5 million ($0.6 million).
  • Total lease liabilities were €14,606 thousand as of June 30, 2026, compared with €15,635 thousand as of December 31, 2025.
  • Accumulated deficit was €(906,294) thousand as of June 30, 2026, compared with €(785,988) thousand as of December 31, 2025.
  • Total shareholders' equity was €399,625 thousand as of June 30, 2026, compared with €484,099 thousand as of December 31, 2025.

Analysis

Immatics reported H1 2026 collaboration revenue of €16,756 thousand, compared with €23,318 thousand in H1 2025. Moderna contributed €13,913 thousand and BMS contributed €2,843 thousand. The company attributed the H1 decline at both partners to a lower proportion of costs incurred relative to overall project budgets. In contrast, second-quarter revenue was €9,144 thousand, compared with €4,737 thousand in the prior-year quarter, aided by higher cost-to-cost revenue recognition and a €0.5 million Moderna milestone.

Development spending accelerated. Research and development expenses were €(121,597) thousand, compared with €(87,014) thousand, led by direct external TCR T-cell therapy program expense of €(47,931) thousand versus €(20,976) thousand. Management attributed that increase primarily to anzu-cel activity, predominantly the SUPRAME study and, to a lesser extent, uveal melanoma. General and administrative expenses rose to €(28,450) thousand from €(24,847) thousand, reflecting commercialization-preparation activities for anzu-cel, professional and consulting fees, personnel costs and software expenses.

The operating result was €(133,267) thousand, compared with €(88,502) thousand. The financial result improved to €12,739 thousand from €(23,698) thousand as other financial expenses declined to €(602) thousand from €(36,113) thousand, principally due to lower foreign-exchange losses. Net loss nevertheless increased to €(120,306) thousand from €(110,204) thousand, while basic and diluted loss per share were each €(0.89), compared with €(0.91).

Liquidity included €232,459 thousand of cash and cash equivalents and €160,891 thousand of other financial assets as of June 30, 2026. Operating cash use was €(102,504) thousand for H1 2026. Financing cash inflow of €20,305 thousand included an ATM issuance of 2,500,000 ordinary shares on March 12, 2026, which generated gross proceeds of €21.6 million ($25.0 million). The company stated that cash, cash equivalents and other financial assets of €393.4 million are sufficient to fund operations through at least the next 12 months.

Operationally, SUPRAME enrollment remains on track to complete required randomizations by year-end, but PFS events are occurring more slowly than originally modeled. Immatics plans a single streamlined final PFS analysis with a lower prespecified number of events, while increasing planned enrollment by approximately 90 patients to approximately 450 patients to raise statistical power for overall survival. The company expects final PFS topline data in the first half of 2027 and a BLA submission in 2027. A Moderna-sponsored clinical trial dosed its first patient in July 2026, triggering a milestone payment to Immatics.

Not in the filing

stated, not guessed
  • Product revenue was not reported because the company has not generated revenue from the sale of pharmaceutical products.
  • Gross profit, cost of revenue and gross margin were not reported.
  • Non-GAAP or adjusted financial metrics were not reported.
  • Forward revenue, gross-margin, operating-expense and tax-rate guidance was not reported.
  • A formal debt balance other than lease liabilities was not reported.
  • Share repurchases and dividends were not reported.
  • Percentage year-over-year and quarter-over-quarter changes for the reported metrics were not printed.
  • Named executive quotes were not included in the filing.

Written by an AI language model from the company’s SEC earnings filing (Form 8-K Item 2.02, or Form 6-K for a foreign private issuer). Every figure is checked against the filing text, and a metric the filing does not print, or whose value, prior period and change do not add up, is dropped from the metrics. The model can still misread a table, in the metrics or in the text, so check a number in the filing before you rely on it. Consensus estimates, price targets and share-price reactions are not shown because they are not in the filing. AI-generated research, not investment advice.

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