Immatics Announces Second Quarter 2025 Financial Results and Business Update
Immatics (NASDAQ: IMTX) reported Q2 2025 financial results and provided updates on its PRAME-targeting therapies. The company's lead candidate, anzu-cel, demonstrated strong results in Phase 1b melanoma trials with a 56% confirmed objective response rate and 12.1 months median duration of response. The global Phase 3 SUPRAME trial is progressing with interim and final analyses expected in 2026.
Financial highlights include cash position of $560.5 million providing runway into 2H 2027, though Q2 showed increased net loss of $82.4 million versus $21.1 million year-over-year. R&D expenses rose to $52.9 million, reflecting advancement of clinical programs.
The company announced CFO Arnd Christ's planned departure and is searching for a replacement. Multiple clinical updates across its pipeline are expected in Q4 2025, including data from IMA203CD8, IMA402, and IMA401 programs.
Immatics (NASDAQ: IMTX) ha comunicato i risultati finanziari del 2° trimestre 2025 e fornito aggiornamenti sulle terapie mirate a PRAME. Il candidato principale, anzu-cel, ha mostrato risultati solidi nella fase 1b sul melanoma con un tasso di risposta obiettiva confermata del 56% e una durata mediana della risposta di 12,1 mesi. Lo studio globale di fase 3 SUPRAME è in corso, con analisi intermedie e finali previste per il 2026.
Tra i punti finanziari, una liquidità di 560,5 milioni di dollari che garantisce cassa fino alla seconda metà del 2027, sebbene nel 2° trimestre la perdita netta sia aumentata a 82,4 milioni di dollari rispetto a 21,1 milioni nell'anno precedente. Le spese di R&S sono salite a 52,9 milioni di dollari, a riflesso dell'avanzamento dei programmi clinici.
L'azienda ha annunciato l'uscita prevista del CFO Arnd Christ e sta cercando un sostituto. Sono attesi diversi aggiornamenti clinici nel 4° trimestre 2025, inclusi dati dai programmi IMA203CD8, IMA402 e IMA401.
Immatics (NASDAQ: IMTX) informó resultados financieros del 2T 2025 y dio novedades sobre sus terapias dirigidas a PRAME. El candidato principal, anzu-cel, mostró resultados sólidos en la fase 1b para melanoma con una tasa de respuesta objetiva confirmada del 56% y una mediana de duración de la respuesta de 12,1 meses. El ensayo global de fase 3 SUPRAME avanza y se esperan análisis intermedios y finales en 2026.
Entre los aspectos financieros, dispone de 560,5 millones de dólares en efectivo, lo que proporciona financiación hasta la segunda mitad de 2027, aunque en el 2T registró una pérdida neta mayor de 82,4 millones de dólares frente a 21,1 millones interanual. Los gastos en I+D aumentaron a 52,9 millones de dólares, reflejando el avance de los programas clínicos.
La compañía anunció la salida prevista del CFO Arnd Christ y está buscando un reemplazo. Se esperan múltiples actualizaciones clínicas en el 4T 2025, incluidos datos de los programas IMA203CD8, IMA402 e IMA401.
Immatics (NASDAQ: IMTX)는 2025년 2분기 재무실적을 발표하고 PRAME 표적 치료제의 최신 현황을 알렸습니다. 주력 후보물질 anzu-cel은 흑색종 대상 1b상에서 확증된 객관적 반응률 56%와 반응 지속기간 중앙값 12.1개월이라는 우수한 결과를 보였습니다. 글로벌 3상 SUPRAME 임상은 진행 중이며, 중간분석과 최종분석은 2026년에 예정되어 있습니다.
재무 하이라이트로는 현금 560.5 million 달러로 2027년 하반기까지 자금 여력이 확보되어 있으나, 2분기 순손실은 전년 동기 대비 증가하여 82.4 million 달러를 기록했습니다(전년 동기 21.1 million 달러). 연구개발비는 임상 프로그램 진전에 따라 52.9 million 달러로 늘었습니다.
회사는 최고재무책임자(CFO) 아른트 크리스트(Arnd Christ)의 퇴임 계획을 발표하고 후임자를 찾고 있습니다. IMA203CD8, IMA402, IMA401 프로그램을 포함한 다수의 임상 업데이트가 2025년 4분기에 예정되어 있습니다.
Immatics (NASDAQ: IMTX) a publié ses résultats financiers du 2T 2025 et fait le point sur ses thérapies ciblant PRAME. Le candidat principal, anzu-cel, a obtenu de bons résultats en phase 1b sur le mélanome avec un taux de réponse objective confirmé de 56% et une durée médiane de réponse de 12,1 mois. L'essai mondial de phase 3 SUPRAME est en cours, avec des analyses intermédiaire et finale prévues en 2026.
Parmi les points financiers, une trésorerie de 560,5 millions de dollars offrant une visibilité jusqu'au second semestre 2027, malgré une perte nette en hausse au 2T de 82,4 millions de dollars contre 21,1 millions un an plus tôt. Les dépenses de R&D ont augmenté à 52,9 millions de dollars, reflétant l'avancement des programmes cliniques.
La société a annoncé le départ prévu du directeur financier Arnd Christ et recherche son remplaçant. Plusieurs mises à jour cliniques du portefeuille sont attendues au 4T 2025, notamment des données sur les programmes IMA203CD8, IMA402 et IMA401.
Immatics (NASDAQ: IMTX) legte die Finanzergebnisse für Q2 2025 vor und informierte über Fortschritte bei PRAME-gerichteten Therapien. Der führende Kandidat anzu-cel zeigte in Phase-1b-Studien beim Melanom starke Ergebnisse mit einer bestätigten objektiven Ansprechrate von 56% und einer mediane Ansprechdauer von 12,1 Monaten. Die globale Phase-3-Studie SUPRAME läuft; Zwischen- und Abschlussanalysen sind für 2026 geplant.
Zu den finanziellen Kennzahlen zählt eine Barreserve von 560,5 Millionen US-Dollar, die Mittel bis in die zweite Hälfte 2027 sichern soll, obwohl im Q2 der Nettoverlust auf 82,4 Millionen US-Dollar gegenüber 21,1 Millionen im Vorjahreszeitraum gestiegen ist. Die F&E-Ausgaben stiegen auf 52,9 Millionen US-Dollar, was die Weiterentwicklung der klinischen Programme widerspiegelt.
Das Unternehmen kündigte den geplanten Weggang des CFO Arnd Christ an und sucht einen Nachfolger. Für Q4 2025 werden mehrere klinische Updates erwartet, darunter Daten zu den Programmen IMA203CD8, IMA402 und IMA401.
- Strong Phase 1b results for anzu-cel with 56% confirmed objective response rate
- Healthy cash position of $560.5 million with runway into 2H 2027
- Phase 3 SUPRAME trial progressing well with analyses expected in 2026
- Milestone payment received from Moderna collaboration
- Net loss increased significantly to $82.4 million from $21.1 million year-over-year
- R&D expenses increased to $52.9 million from $41.3 million year-over-year
- Revenue decreased to $5.5 million from $22.0 million year-over-year
- CFO departure announced, creating potential leadership transition uncertainty
Insights
Immatics shows promising clinical data for PRAME therapies with strong melanoma responses, though cash burn accelerates amid advancing trials.
Immatics' lead PRAME cell therapy anzu-cel continues to demonstrate compelling clinical data in melanoma patients. The 56% confirmed objective response rate with 12.1 months median duration of response in heavily pretreated melanoma patients stands out as particularly impressive compared to current standards of care. More notable is the 67% response rate in uveal melanoma, a notoriously difficult-to-treat cancer with few effective options.
The company is executing a comprehensive development strategy across their PRAME franchise. Their pivotal SUPRAME Phase 3 trial is advancing with interim and final analyses expected in 2026, positioning anzu-cel for potential BLA submission in 1H 2027 and commercial launch in 2H 2027. This timeline appears realistic given current enrollment rates.
Financially, Immatics reported
The quarterly net loss of
The announcement of CFO Arnd Christ's planned departure introduces some management uncertainty as Immatics approaches commercialization. This transition period will require careful management to maintain operational continuity during a critical development phase.
Immatics is building a comprehensive PRAME-targeted oncology platform with multiple modalities (cell therapies and bispecifics) addressing different patient populations. With four active clinical programs (anzu-cel, IMA203CD8, IMA402, and IMA401) and multiple data readouts expected in Q4 2025, the next six months will be pivotal in validating their approach across different cancer types.
- Anzu-cel (anzutresgene autoleucel, IMA203) PRAME Cell Therapy: One-time infusion continues to show favorable tolerability as well as strong anti-tumor activity and durability in 33 heavily pretreated patients with metastatic melanoma in data from a Phase 1b trial presented at the 2025 ASCO Annual Meeting:
56% cORR, 12.1 months mDOR at 13.4 months mFU, 6.1 months mPFS and 15.9 months mOS - Anzu-cel (IMA203) PRAME Cell Therapy: Global, randomized, controlled Phase 3 trial, SUPRAME, in previously treated advanced melanoma ongoing; interim and final analyses will occur in 2026
- IMA203CD8 PRAME Cell Therapy (GEN2): Phase 1a clinical trial ongoing with next data update, including dose escalation data in ovarian cancer, melanoma and synovial sarcoma, planned in 4Q 2025
- IMA402 PRAME Bispecific: Phase 1a clinical trial in solid tumors ongoing with next data update with a focus on melanoma at relevant dose levels planned in 4Q 2025
- IMA401 MAGEA4/8 Bispecific: Phase 1a clinical trial, including a checkpoint inhibitor combination, ongoing with next data update with a focus on head and neck cancer planned in 4Q 2025
- Cash and cash equivalents as well as other financial assets of
$560.5 million 1 (€478.2 million ) as of June 30, 2025; cash reach into 2H 2027
Houston, Texas and Tuebingen, Germany, August 13, 2025 – Immatics N.V. (NASDAQ: IMTX, “Immatics” or the “Company”), a clinical-stage biopharmaceutical company and the global leader in precision targeting of PRAME, today provided a business update and reported financial results for the quarter ended June 30, 2025.
“The presentation of positive and extended follow-up Phase 1b data at ASCO has further strengthened our conviction in the transformative therapeutic potential of our PRAME cell therapy, anzu-cel, in patients with advanced cutaneous and uveal melanoma,” said Harpreet Singh, Ph.D., Chief Executive Officer and Co-Founder of Immatics. “The advancement of the SUPRAME Phase 3 trial remains our top priority as we strive to bring anzu-cel to the market for patients with unmet medical need. In addition, Immatics is building the broadest PRAME franchise with the most PRAME indications and modalities. In the coming months, we look forward to delivering updates on our next-generation, half-life extended PRAME bispecific, IMA402, our second-generation PRAME cell therapy, IMA203CD8, as well as data beyond PRAME from IMA401, our bispecific targeting MAGEA4/8.”
Second Quarter 2025 and Subsequent Company Progress
PRAME Franchise
Anzu-cel (IMA203) PRAME Cell Therapy – Market Entry in Advanced Melanoma
Anzu-cel (anzutresgene autoleucel), previously called IMA203, is Immatics’ lead PRAME cell therapy and will be the Company’s first PRAME therapy to enter the market in advanced melanoma. The current addressable patient population for anzu-cel’s first target indications, second-line or later (2L) cutaneous melanoma as well as metastatic uveal melanoma, includes ~9,000 patients2.
Phase 3 trial, SUPRAME, for anzu-cel (IMA203) in previously treated, advanced cutaneous melanoma
- Immatics’ global, randomized, controlled, multi-center Phase 3 clinical trial, SUPRAME, is currently ongoing to evaluate the efficacy, safety and tolerability of anzu-cel PRAME cell therapy vs. investigator's choice in patients with unresectable or metastatic cutaneous melanoma who have received prior treatment with a checkpoint inhibitor.
- SUPRAME is designed as a well-controlled clinical trial evaluating anzu-cel as a monotherapy in a late-stage cutaneous melanoma patient population and is intended to generate robust data to support regulatory approval of anzu-cel as Immatics advances this PRAME cell therapy towards the market.
- Primary endpoint for seeking full approval will be blinded independent central review (“BICR”)-assessed (RECIST v1.1) progression-free survival (PFS). Secondary endpoints include overall survival (OS), objective response rate (ORR), safety and patient-reported outcomes about quality of life.
- Pre-specified interim and final data analyses will be triggered upon the occurrence of a defined number of events for PFS (progressive disease or death). Data from the interim analysis is not intended to be published to protect the integrity of the ongoing clinical trial.
- The Company remains on track for planned BLA submission in 1H 2027 and launch of anzu-cel in 2H 2027. Given the event-driven nature of the clinical trial design and based on the clinical site activation timelines, the target number of clinical trial sites and the current strong enrollment rate, Immatics estimates that the interim and final analyses will occur in 2026.
- Patient recruitment is currently ongoing in the US and Germany. The SUPRAME trial is planned to be conducted in more than 65 sites across North America and Europe, including the US, Germany, France, the Netherlands, the UK and Canada.
Phase 1b trial for anzu-cel (IMA203) PRAME cell therapy in patients with metastatic melanoma
- On May 31, 2025, extended follow-up data from the Phase 1b trial of anzu-cel in metastatic melanoma were presented by Martin Wermke, MD, in an oral presentation at the 2025 ASCO Annual Meeting. The data further substantiate Immatics’ global leadership in precision targeting of PRAME and the potential of anzu-cel to be the Company’s first PRAME product to enter the market. A one-time infusion of anzu-cel PRAME cell therapy in all melanoma patients demonstrated favorable tolerability and promising clinical activity: cORR of
56% ; mDOR of 12.1 months at mFU of 13.4 months; mPFS of 6.1 months; mOS of 15.9 months- Cutaneous melanoma subgroup, all post-checkpoint inhibitor, showed cORR of
50% , mDOR not reached at mFU of 16.7 months; mPFS of 6.0 months - Uveal melanoma subgroup, majority post-tebentafusp and checkpoint inhibitor, showed cORR of
67% , mDOR of 11.0 months at mFU of 13.4 months; mPFS of 8.5 months
- Cutaneous melanoma subgroup, all post-checkpoint inhibitor, showed cORR of
Anzu-cel (IMA203) PRAME cell therapy in patients with uveal melanoma
- Immatics will continue to evaluate anzu-cel in patients with uveal melanoma through the ongoing Phase 1b clinical trial. In addition, a Phase 2 cohort for ~30 patients with uveal melanoma is planned to commence in 4Q 2025.
- Uveal melanoma data from the Phase 1b trial that support the Phase 2 cohort will be presented by Sapna Patel, MD, in a proffered paper presentation at the European Society for Medical Oncology (ESMO) Congress 2025 on October 20, 2025.
IMA203CD8 PRAME Cell Therapy (GEN2) – Expansion to all Advanced PRAME Cancers
IMA203CD8 is the Company’s second-generation PRAME cell therapy product candidate being developed with the goal of expanding into all advanced PRAME cancers. Given its enhanced pharmacology profile, once the target dose is reached, the Company intends to pursue the clinical development of this product with a tumor-agnostic approach, starting with gynecologic cancers.
- Phase 1a dose escalation in solid tumors is ongoing to evaluate higher doses of IMA203CD8 with and without IL-2.
- The next clinical trial update, which will report on the continued dose escalation in multiple PRAME cancers, including ovarian cancer, melanoma and synovial sarcoma treated at relevant doses, is planned for 4Q 2025.
IMA402 PRAME Bispecific – Expansion to Early-Stage PRAME Cancers
To expand the PRAME opportunity to early-stage PRAME cancers, the Company is developing its off-the-shelf, next-generation, half-life extended TCR Bispecific, IMA402. Upon delivering clinical proof-of-concept (“PoC”) in last-line melanoma, Immatics plans to explore its potential in gynecologic cancers, non-small cell lung cancer (NSCLC), breast cancer and other solid tumor indications as well as earlier treatment lines of solid cancers, such as first-line (1L) cutaneous melanoma.
- Phase 1a dose escalation is ongoing, and the next update with clinical data at relevant dose levels with a focus on second-line or later (2L) melanoma is planned for 4Q 2025.
Beyond the PRAME Franchise
IMA401 MAGEA4/8 Bispecific – Driving Innovation Beyond PRAME
Immatics is driving innovation beyond PRAME by evaluating its off-the-shelf, next-generation, half-life extended TCR Bispecific, IMA401, targeting MAGEA4/8 in patients with NSCLC, head & neck cancer, bladder cancer and other solid tumor indications, with the primary goal of developing this product candidate in earlier treatment lines.
- Dose refinement in the Phase 1a trial evaluating IMA401 as a monotherapy and in combination with a checkpoint inhibitor is ongoing with a focus on indications with high MAGEA4/8 target expression, such as lung and head and neck cancer.
- The Company expects to report updated data with a focus on head and neck cancer in 4Q 2025. Data with a focus on NSCLC are expected in 2026.
Corporate Development
- The Company’s Chief Financial Officer, Arnd Christ, has informed the Company that he intends to transition out of the Company to pursue other opportunities. Arnd Christ has served as Chief Financial Officer of Immatics since 2020 and has been instrumental in driving the Company’s maturation as a publicly listed entity. He will be stepping down as Immatics enters its next phase of development and transitions to become a commercial-stage organization. The Company is commencing a search for his replacement. Arnd Christ will remain as the Company’s CFO to ensure a smooth transition until the earlier of the appointment of his successor or the end of 1Q 2026.
- Moderna Collaboration: Immatics generated regulatory support data for one of Moderna’s mRNA product candidates that leveraged Immatics’ XPRESIDENT® and its bioinformatics and AI platform XCUBE™. Pursuant to the 2023 Collaboration Agreement under the Database/Vaccine Program, Immatics received a milestone payment triggered by the initiation of the first Phase 1 clinical trial for the Moderna product candidate.
- International Nonproprietary Name: The International Nonproprietary Names (INN) Expert Committee of the World Health Organization selected anzutresgene autoleucel (anzu-cel) as the INN for Immatics’ PRAME cell therapy, previously known as IMA203. Each INN, often called a generic name, is a distinct and globally recognized designation used to identify pharmaceutical substances or active ingredients.
Second Quarter 2025 Financial Results
Cash Position: Cash and cash equivalents as well as other financial assets total
Revenue: Total revenue, consisting of revenue from collaboration agreements, was
Research and Development Expenses: R&D expenses were
General and Administrative Expenses: G&A expenses were
Net Profit and Loss: Net loss was
Full financial statements can be found in our Report on 6-K filed with the Securities and Exchange Commission (SEC) on August 13, 2025, and published on the SEC website under www.sec.gov.
Upcoming Investor Conferences
- Cantor Global Healthcare Conference, New York (NY) – September 3 - 5, 2025
- Jefferies Global Healthcare Conference, London, United Kingdom – November 17 - 20, 2025
To see the full list of events and presentations, visit: https://investors.immatics.com/events-presentations.
About PRAME
PRAME is a target expressed in more than 50 cancers. Immatics is the global leader in precision targeting of PRAME and has the broadest PRAME franchise with the most PRAME indications and modalities. The Immatics PRAME franchise currently includes three product candidates, two therapeutic modalities and a combination therapy that target PRAME: anzu-cel (anzutresgene autoleucel, IMA203) PRAME cell therapy, IMA203CD8 PRAME cell therapy (GEN2), IMA402 PRAME bispecific and anzu-cel in combination with Moderna’s PRAME adaptive immune modulating therapy.
About Immatics
Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets. This deep know-how is the foundation for our pipeline of Adoptive Cell Therapies and TCR Bispecifics as well as our partnerships with global leaders in the pharmaceutical industry. We are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer.
Immatics intends to use its website www.immatics.com as a means of disclosing material non-public information. For regular updates you can also follow us on LinkedIn and Instagram.
Forward-Looking Statements
Certain statements in this press release may be considered forward-looking statements. Forward-looking statements generally relate to future events or the Company’s future financial or operating performance. For example, statements concerning timing of data read-outs for product candidates, the timing, outcome and design of clinical trials, the nature of clinical trials (including whether such clinical trials will be registration-enabling), the timing of IND, CTA or BLA filings, estimated market opportunities of product candidates, the Company’s focus on partnerships to advance its strategy, and other metrics are forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as “may”, “should”, “expect”, “plan”, “target”, “intend”, “will”, “estimate”, “anticipate”, “believe”, “predict”, “potential” or “continue”, or the negatives of these terms or variations of them or similar terminology. Such forward-looking statements are subject to risks, uncertainties, and other factors which could cause actual results to differ materially from those expressed or implied by such forward-looking statements. These forward-looking statements are based upon estimates and assumptions that, while considered reasonable by Immatics and its management, are inherently uncertain. New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. Factors that may cause actual results to differ materially from current expectations include, but are not limited to, various factors beyond management's control including general economic conditions and other risks, uncertainties and factors set forth in the Company’s Annual Report on Form 20-F and other filings with the Securities and Exchange Commission (SEC). Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements, which speak only as of the date they are made. The Company undertakes no duty to update these forward-looking statements. All the scientific and clinical data presented within this press release are – by definition prior to completion of the clinical trial and a clinical study report – preliminary in nature and subject to further quality checks including customary source data verification.
For more information, please contact:
Media
Trophic Communications
Phone: +49 151 74416179
immatics@trophic.eu
Immatics N.V.
Jordan Silverstein
Head of Strategy
Phone: +1 346 319-3325
InvestorRelations@immatics.com
Immatics N.V. and subsidiaries
Condensed Consolidated Statement of Loss of Immatics N.V.
| | | Three months ended June 30, | | | | Six months ended June 30, | | ||||||||||
| | | 2025 | | | 2024 | | | | 2025 | | | 2024 | | ||||
| | | (Euros in thousands, except per share data) | | | | (Euros in thousands, except per share data) | | ||||||||||
| Revenue from collaboration agreements | | | 4,737 | | | | 18,755 | | | | | 23,318 | | | | 49,024 | |
| Research and development expenses | | | (45,106 | ) | | | (35,216 | ) | | | | (87,014 | ) | | | (67,324 | ) |
| General and administrative expenses | | | (12,780 | ) | | | (10,128 | ) | | | | (24,847 | ) | | | (21,770 | ) |
| Other income | | | 22 | | | | 25 | | | | | 41 | | | | 37 | |
| Operating result | | | (53,127 | ) | | | (26,564 | ) | | | | (88,502 | ) | | | (40,033 | ) |
| Change in fair value of liabilities for warrants | | | 133 | | | | (648 | ) | | | | 1,730 | | | | 395 | |
| Other financial income | | | 4,421 | | | | 9,665 | | | | | 10,685 | | | | 20,580 | |
| Other financial expenses | | | (22,776 | ) | | | (305 | ) | | | | (36,113 | ) | | | (515 | ) |
| Financial result | | | (18,222 | ) | | | 8,712 | | | | | (23,698 | ) | | | 20,460 | |
| Loss before taxes | | | (71,349 | ) | | | (17,852 | ) | | | | (112,200 | ) | | | (19,573 | ) |
| Taxes on income | | | 1,001 | | | | (140 | ) | | | | 1,996 | | | | (660 | ) |
| Net loss | | | (70,348 | ) | | | (17,992 | ) | | | | (110,204 | ) | | | (20,233 | ) |
| Net loss per share: | | | | | | | | | | | | | | ||||
| Basic | | | (0.58 | ) | | | (0.17 | ) | | | | (0.91 | ) | | | (0.20 | ) |
| Diluted | | | (0.58 | ) | | | (0.17 | ) | | | | (0.91 | ) | | | (0.20 | ) |
Immatics N.V. and subsidiaries
Condensed Consolidated Statement of Comprehensive Loss of Immatics N.V.
| | | Three months ended June 30, | | | | Six months ended June 30, | | ||||||||||
| | 2025 | | | 2024 | | | | 2025 | | | 2024 | | |||||
| | (Euros in thousands) | | | | (Euros in thousands) | | |||||||||||
| Net loss | | | (70,348 | ) | | | (17,992 | ) | | | | (110,204 | ) | | | (20,233 | ) |
| Other comprehensive income/(loss) | | | | | | | | | | | | | | ||||
| Items that may be reclassified subsequently to profit or loss | | | | | | | | | | | | | | ||||
| Currency translation differences from foreign operations | | | (5,833 | ) | | | 462 | | | | | (8,544 | ) | | | 798 | |
| Total comprehensive loss for the period | | | (76,181 | ) | | | (17,530 | ) | | | | (118,748 | ) | | | (19,435 | ) |
Immatics N.V. and subsidiaries
Condensed Consolidated Statement of Financial Position of Immatics N.V.
| | | As of | | |||||
| | June 30, 2025 | | | December 31, 2024 | | |||
| | (Euros in thousands) | | ||||||
| Assets | | | | | | | ||
| Current assets | | | | | | | ||
| Cash and cash equivalents | | | 256,635 | | | | 236,748 | |
| Other financial assets | | | 221,551 | | | | 367,704 | |
| Accounts receivables | | | 1,962 | | | | 5,857 | |
| Other current assets | | | 23,788 | | | | 19,246 | |
| Total current assets | | | 503,936 | | | | 629,555 | |
| Non-current assets | | | | | | | ||
| Property, plant and equipment | | | 46,306 | | | | 50,380 | |
| Intangible assets | | | 1,598 | | | | 1,629 | |
| Right-of-use assets | | | 14,462 | | | | 13,332 | |
| Other non-current assets | | | 1,000 | | | | 1,250 | |
| Total non-current assets | | | 63,366 | | | | 66,591 | |
| Total assets | | | 567,302 | | | | 696,146 | |
| Liabilities and shareholders’ equity | | | | | | | ||
| Current liabilities | | | | | | | ||
| Provisions | | | 4,391 | | | | — | |
| Accounts payables | | | 18,701 | | | | 20,693 | |
| Deferred revenue | | | 24,389 | | | | 35,908 | |
| Liabilities for warrants | | | — | | | | 1,730 | |
| Lease liabilities | | | 3,004 | | | | 2,851 | |
| Other current liabilities | | | 6,762 | | | | 6,805 | |
| Total current liabilities | | | 57,247 | | | | 67,987 | |
| Non-current liabilities | | | | | | | ||
| Deferred revenue | | | 27,561 | | | | 34,161 | |
| Lease liabilities | | | 14,112 | | | | 13,352 | |
| Deferred tax liability | | | 3,808 | | | | 5,804 | |
| Total non-current liabilities | | | 45,481 | | | | 53,317 | |
| Shareholders’ equity | | | | | | | ||
| Share capital | | | 1,216 | | | | 1,216 | |
| Share premium | | | 1,170,616 | | | | 1,162,136 | |
| Accumulated deficit | | | (699,745 | ) | | | (589,541) | |
| Other reserves | | | (7,513 | ) | | | 1,031 | |
| Total shareholders’ equity | | | 464,574 | | | | 574,842 | |
| Total liabilities and shareholders’ equity | | | 567,302 | | | | 696,146 | |
Immatics N.V. and subsidiaries
Condensed Consolidated Statement of Cash Flows of Immatics N.V.
| | | Six months ended June 30, | | |||||
| | 2025 | | | 2024 | | |||
| | (Euros in thousands) | | ||||||
| Cash flows from operating activities | | | | | | | ||
| Net loss | | | (110,204 | ) | | | (20,233 | ) |
| Taxes on income | | | (1,996 | ) | | | 660 | |
| Loss before tax | | | (112,200 | ) | | | (19,573 | ) |
| Adjustments for: | | | | | | | ||
| Interest income | | | (9,719 | ) | | | (12,660 | ) |
| Depreciation and amortization | | | 6,166 | | | | 6,116 | |
| Interest expenses | | | 493 | | | | 420 | |
| Equity-settled share-based payment | | | 8,471 | | | | 8,605 | |
| Net foreign exchange differences and expected credit losses | | | 34,241 | | | | (7,723 | ) |
| Change in fair value of liabilities for warrants | | | (1,730 | ) | | | (395 | ) |
| Gains from disposal of fixed assets | | | 40 | | | | 1 | |
| Changes in: | | | | | | | ||
| Decrease in accounts receivables | | | 3,894 | | | | 1,283 | |
| (Increase)/decrease in other assets | | | (277 | ) | | | 766 | |
| Decrease in deferred revenue, accounts payables and other liabilities | | | (15,534 | ) | | | (48,493 | ) |
| Interest received | | | 18,012 | | | | 8,260 | |
| Interest paid | | | (493 | ) | | | (420 | ) |
| Income tax paid | | | (5,445 | ) | | | (2,012 | ) |
| Income tax refunded | | | 820 | | | | — | |
| Net cash used in operating activities | | | (73,261 | ) | | | (65,825 | ) |
| Cash flows from investing activities | | | | | | | ||
| Payments for property, plant and equipment | | | (4,503 | ) | | | (11,797 | ) |
| Payments for intangible assets | | | (190 | ) | | | (148 | ) |
| Proceeds from disposal of property, plant and equipment | | | 47 | | | | — | |
| Payments for investments classified in Other financial assets | | | (280,651 | ) | | | (356,596 | ) |
| Proceeds from maturity of investments classified in Other financial assets | | | 396,353 | | | | 196,548 | |
| Net cash provided by/(used in) investing activities | | | 111,056 | | | | (171,993 | ) |
| Cash flows from financing activities | | | | | | | ||
| Net proceeds from issuance of shares to equity holders | | | 9 | | | | 174,476 | |
| Payments of lease liabilities | | | (1,473 | ) | | | (397 | ) |
| Net cash provided by/(used in) financing activities | | | (1,464 | ) | | | 174,079 | |
| Net increase/(decrease) in cash and cash equivalents | | | 36,331 | | | | (63,739 | ) |
| Cash and cash equivalents at the beginning of the period | | | 236,748 | | | | 218,472 | |
| Effects of exchange rate changes and expected credit losses on cash and cash equivalents | | | (16,444 | ) | | | 3,410 | |
| Cash and cash equivalents at the end of the period | | | 256,635 | | | | 158,143 | |
Immatics N.V. and subsidiaries
Condensed Consolidated Statement of Changes in Shareholders’ Equity of Immatics N.V.
| (Euros in thousands) | | Share capital | | | Share premium | | | Accumulated deficit | | | Other reserves | | | Total share- holders’ equity | | |||||
| Balance as of January 1, 2024 | | | 847 | | | | 823,166 | | | | (604,759 | ) | | | (1,636 | ) | | | 217,618 | |
| Other comprehensive income | | | — | | | | — | | | — | | | | 798 | | | | 798 | | |
| Net loss | | | — | | | | — | | | | (20,233 | ) | | | — | | | | (20,233 | ) |
| Comprehensive income/(loss) for the period | | | — | | | | — | | | | (20,233 | ) | | | 798 | | | | (19,435 | ) |
| Equity-settled share-based compensation | | | — | | | | 8,605 | | | | — | | | | — | | | | 8,605 | |
| Share options exercised | | | 1 | | | | 1,036 | | | | — | | | | — | | | | 1,037 | |
| Issue of share capital – net of transaction costs | | | 183 | | | | 173,257 | | | | — | | | | — | | | | 173,440 | |
| Balance as of June 30, 2024 | | | 1,031 | | | | 1,006,064 | | | | (624,992 | ) | | | (838 | ) | | | 381,265 | |
| Balance as of January 1, 2025 | | | 1,216 | | | | 1,162,136 | | | | (589,541 | ) | | | 1,031 | | | | 574,842 | |
| Other comprehensive loss | | | — | | | | — | | | | — | | | | (8,544 | ) | | | (8,544 | ) |
| Net loss | | | — | | | | — | | | | (110,204 | ) | | | — | | | | (110,204 | ) |
| Comprehensive loss for the period | | | — | | | | — | | | | (110,204 | ) | | | (8,544 | ) | | | (118,748 | ) |
| Equity-settled share-based compensation | | | — | | | | 8,471 | | | | — | | | | — | | | | 8,471 | |
| Share options exercised | | | — | | | | 9 | | | | — | | | | — | | | | 9 | |
| Balance as of June 30, 2025 | | | 1,216 | | | | 1,170,616 | | | | (699,745 | ) | | | (7,513 | ) | | | 464,574 | |
1 All amounts translated using the exchange rate published by the European Central Bank in effect as of June 30, 2025 (1 EUR = 1.172 USD).
2 Refers to PRAME+/HLA-A*02:01+ patients in the US and EU5 in 2025; Source: Clarivate Disease Landscape and Forecast
Attachment
FAQ
What were Immatics (IMTX) key Q2 2025 financial results?
What were the Phase 1b trial results for Immatics' anzu-cel in melanoma patients?
When will Immatics (IMTX) report next clinical updates for its pipeline?
What is the cash runway for Immatics (IMTX)?
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