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EXACT Therapeutics AS

Investor Presentation Nov 25, 2025

3600_rns_2025-11-25_37e3572e-258e-4da3-9cf7-bcc2c011b41c.pdf

Investor Presentation

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Defeating barriers - in solid tumours

DNB Carnegie Nordic Healthcare Conference 25 November, 2025

Important notice and disclaimer

This presentation (the "Presentation") has been prepared by EXACT Therapeutics AS (the "Company") exclusively for information purposes.

The Presentation is being made only to, and is only directed at, persons to whom such presentation may lawfully be communicated ('relevant persons'). Any person who is not a relevant person should not act or rely on the Presentation or any of its contents.

The Presentation does not constitute an offering of securities or otherwise constitute an invitation or inducement to any person to underwrite, subscribe for or otherwise acquire securities in the Company. The release, publication or distribution of the Presentation in certain jurisdictions may be restricted by law, and therefore persons in such jurisdictions into which this Presentation is released, published or distributed should inform themselves about, and observe, such restrictions.

The Presentation contains certain forward-looking statements relating to the business, products, financial performance and results of the Company and its subsidiaries and/or the industry in which they operates. Forward-looking statements concern future circumstances and results and other statements that are not historical facts, sometimes identified by the words "believes", expects", "predicts", "intends", "projects", "plans", "estimates", "aims", "foresees", "anticipates", "targets", and similar expressions. The forwardlooking statements contained in the Presentation, including assumptions, opinions and views of the Company or cited from third party sources are solely opinions and forecasts which are subject to risks, uncertainties and other factors that may cause actual events to differ materially from any anticipated development. Neither the Company nor its employees provides any assurance that the assumptions underlying such forward-looking statements are free from errors nor does any of them accept any responsibility for the future accuracy of the opinions expressed in the Presentation or the actual occurrence of the forecasted developments. The Company assumes no obligation, except as required by law, to update any forward-looking statements or to conform these forward-looking statements to its actual results.

The Presentation contains information obtained from third parties. You are advised that such third party information has not been prepared specifically for inclusion in the Presentation and the Company has not undertaken any independent investigation to confirm the accuracy or completeness of such information.

Several factors could cause the actual results, performance or achievements of the Company to be materially different from any future results, performance or achievements that may be expressed or implied by statements and information in the Presentation, including, among others, the risk factors described in the Company's annual reports. Should any risks or uncertainties materialise, or should underlying assumptions prove incorrect, actual results may vary materially from those described in the Presentation. No representation or warranty (express or implied) is made as to, and no reliance should be placed on, any information, including projections, estimates, targets and opinions, contained herein, and no liability whatsoever is accepted as to any errors, omissions or misstatements contained herein, and, accordingly, neither the Company, its subsidiaries, nor their directors or employees accepts any liability whatsoever arising directly or indirectly from the use of the Presentation.

By attending or receiving the Presentation you acknowledge that you will be solely responsible for your own assessment of the market and the market position of the Company and that you will conduct your own analysis and be solely responsible for forming your own view of the potential future performance of the Company's business. The Presentation speaks as of November 2024. Neither the delivery of this Presentation nor any further discussions of the Company with any of the recipients shall, under any circumstances, create any implication that there has been no change in the affairs of the Company since such date.

EXACT – a frontrunner in ultrasound mediated oncology therapy

We are building a leading biotech company, utilising the power of ultrasound to unlock targeted oncology treatments

  • Spin-out from GE HealthCare focused oncology development strategy:
  • PS101, proprietary fully-owned compound
  • Versatile technology with clinical proof-of-concept in Phase 1 oncology trial final results: 4x increase in percent tumour shrinkage vs SoC alone (liver metastases) & excellent safety
  • Ongoing Phase 2 trial in U.S. and U.K. in first line locally advanced pancreatic cancer
  • Broad IP coverage across all major markets, covering many use areas of the technology
  • Raised 13m USD excl. warrants in Dec. 2024. GE Healthcare as anchor, with participation from other investors including Invus Public Equity. Listed on Euronext Growth, Oslo [EXTX]

Therapeutic ultrasound space is gaining momentum Deal flow is increasing

  • 2023: Carthera raised 45m USD
  • 2024: Insightec raised 150m USD
  • 2024: HistoSonics raised 102m USD
  • 2025: Alphaeus Medical raised 52m USD
  • 2025: Histosonics 2.25b USD acquisition by consortium of investors. This was followed by a 250m USD growth financing

Leading VCs are entering the space.

EXACT Therapeutics | Strategic focus – Oncology first

Pancreatic cancer: Execute on ENACT Phase 2 trial in first line locally advanced pancreatic cancer

  • 2
  • Explore ACT in immuno-oncology: Execute on research collaborations with Agenus Inc. and NRC* grant with ICR*, TGen* and NTNU*

3

CNS cancers and blood-brain barrier: Proof-of-concept in glioblastomaand Blood-Brain Barrier animal models

Pipeline

ACT-enabled oncology pipeline – pancreatic focus

Building on Acoustic Cluster Therapy (ACT) core strengths: defeating barriers in solid tumours

Area / Disease Preclinical Phase I Phase II
Oncology Pancreatic 1) (ENACT Study)
Liver metastases (ACTIVATE study)
Immunotherapy
Glioblastoma
Other CNS 2) diseases
Gene therapy

Notes: 1) Phase 2 trial in 1L locally advanced pancreatic cancer (NCT06850623) 2) CNS – Central Nervous System Source: Company information

The Acoustic Cluster Therapy (ACT) technology defeats biological barriers that hamper drug delivery

  • A noninvasive platform to enable targeted, organ-specific drug delivery
  • ACT treatment is given concomitantly with therapeutics

Source: Company information

A simple and non-invasive treatment process

ACT achieves therapeutic benefit through a 2-step ultrasound process

Step 1: Activation with high frequency (HF)

• • • • • • • • • • • • • • • • • • • •

HF ultrasound is applied for Activation of free-floating microclusters

Resulting in phase shift and formation of large ACT bubbles trapped in capillaries for up to 10 mins

Step 2: Enhancement with low frequency (LF)

LF ultrasound is applied for enhancement by oscillating ACT bubbles

Oscillation of ACT bubbles provides prolonged targeted delivery of therapeutics

Release of ACT bubbles and exhalation through the lungs

8

ACTIVATE Phase 1 trial

– Innovative assessment of anticancer activity Patients with liver metastases of colorectal origin

  • All patients received standard of care treatment
  • One of the liver tumours was treated with ACT
  • Intra-patient comparison of tumour response

Sum of diameters and volume of selected liver metastases

Comparing % change between baseline and Week 8 for insonated vs. control lesions

Assessment by central reviewer, blinded to which lesion was insonated

4x tumour shrinkage compared to control lesions in Phase 1 trial on liver metastases in hard-to-treat patients – presented at ESMO '25

  • ACT significantly enhances the local effect of chemotherapy
  • 9 evaluable hard-to-treat patients with median 4 prior lines of treatment for the 40 μl/kg cohort
  • In the patients who had a response to chemotherapy, ACT-treated tumours showed a significantly greater reduction in diameter compared to control tumours (-29% vs. -7%, p<0.05)
  • Assessment by central reviewer, blinded to which lesion was insonated
  • Excellent safety profile of PS101

4x tumour shrinkage compared to control lesions in Phase 1 trial on liver metastases in hard-to-treat patients – presented at ESMO '25

  • ACT significantly enhances the local effect of chemotherapy
  • 9 evaluable hard-to-treat patients with median 4 prior lines of treatment for the 40 μl/kg cohort
  • In the patients who had a response to chemotherapy, ACT-treated tumours showed a significantly greater reduction in diameter compared to control tumours (-29% vs. -7%, p<0.05)
  • Assessment by central reviewer, blinded to which lesion was insonated
  • Excellent safety profile of PS101

urce: Company Information.

Pancreatic cancer – a high-need, high-opportunity disease

Pancreatic cancer is one of the most lethal cancers and has seen few advances in treatment. More than 67 000 new diagnoses every year in the US alone.

142

die every day in the US1

13%

5-year relative survival1

5

FDA approved drugs

Only 5 direct FDA approvals for PDAC over the last 30 years

ENACT Phase 2 trial status and warrants exercise Two patients treated for >28 days, TMC expected in '25

ACT + mFOLFIRINOX safety and efficacy in first line locally advanced and/or borderline resectable PDAC**

10 sites & 25 patients

Status: 7 sites opened 2 patients treated for >28 days

Safety review

TMC expected before year-end: 3 patients, >28 days of treatment

Trigger warrants exercise

Warrants from Dec '24 placement triggered

Clinical milestones

Interim read-out expected 1H 2026

Final read-out expected 1H 2027

Notes:

Clinicaltrials.gov: NCT06850623 TMC: Trial Monitoring Committee PDAC: Pancreatic Ductal AdenoCarcinoma

Major milestones delivered so far in 2025

Milestone category Description
Oncology (clinical)
Phase 1 ACTIVATE trial Final study results from ACTIVATE trial in patients with liver metastases
of colorectal cancer origin (presented at ESMO* 2025)
Phase 2 ENACT trial USA: Approval of IND for ENACT Phase 2 trial in first line locally
advanced pancreatic cancer by the FDA
First patient dosed in ENACT Phase 2 trial (USA)
Europe: Approval of CTA for ENACT Phase 2 trial by the MHRA
Initial safety read-out from ENACT Phase 2 trial (3 patients)
Technology Expansion (pre-clinical)
Updates on immuno-oncology Testing ACT in immuno-oncology (presented at CICON* 2025)
Updates on CNS/Blood-Brain Barrier Testing ACT on glioblastoma (presented at SNMMI* 2025)
Updates on IP Grant of key patents

* ESMO: European Society for Medical Oncology; CICON: Cancer Immunotherapy Conference; SNMMI: Society of Nuclear Medicine and Molecular Imaging 14

Key take-aways and de-risking

Focused oncology strategy - Phase 2 ENACT trial well underway

Positive clinical and preclinical proof of concept for ACT

1 medical equipment company as vested device and supply partner

Broad granted IP coverage

Rich near-term news flow

ACT® - defeating barriers in solid tumours

Dr Per Walday

CEO

M: +47 917 93 429

E: [email protected]

Caspar Foghsgaard

CBO

M: +47 454 89 233

E: [email protected]

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