Cantargia Ab · OMXSTO:CANTA

Cantargia Ab — Investor Presentation (May 2023)

29 slides from Cantargia Ab's investor presentation, May 2023

  1. Slide 1: Targeting IL1RAP to address unmet needs in severe cancer and autoimmune diseases

    Targeting IL1RAP to address unmet needs in severe cancer and autoimmune diseases Corporate Presentation May 2023 NASDAQ STOCKHOLM MAIN LIST (CANTA.ST)

  2. Slide 2: Safe Harbor Statement

    Safe Harbor Statement Statements in the Investor Presentation, including those regarding the possible or assumed future or other performance of the Company or its industry or other trend projections, constitute forward-looking statements. By their nature, forward-looking statements involve known and

  3. Slide 3: Cantargia – Strategy to improve current cancer therapies

    Cantargia – Strategy to improve current cancer therapies IL1RAP – A NOVEL TARGET WITH SEVERAL OPPORTUNITIES; CURRENT FOCUS ON SYNERGISTIC COMBINATIONS MDSC – Myeloid-Derived Suppressor Cells 3

  4. Slide 4: New strategy to treat cancer supported by clinical results

    New strategy to treat cancer supported by clinical results PROMISING DATA IN PANCREATIC CANCER → Stronger efficacy than expected from chemotherapy → Patients with higher IL1RAP benefit more Nadunolimab Durable response 50% Primary Chemo- Short-term Best change in tumor size tumor therapy response 0%

  5. Slide 5: IL1RAP: Broad application in cancer and autoimmune disease

    IL1RAP: Broad application in cancer and autoimmune disease 5

  6. Slide 6: Nadunolimab and Biological Context

    NADUNOLIMAB AND BIOLOGICAL CONTEXT

  7. Slide 7: IL1RAP overexpressed in most solid tumors

    IL1RAP overexpressed in most solid tumors IL1RAP EXPRESSION IN SOLID TUMOR TYPES SEVERAL TUMOR-PROMOTING CELLS EXPRESSING IL1RAP IN THE TUMOR MICROENVIRONMENT IL1RAP-expressing tumors 100 75 50 25 0 l C C st al ic er er ta SC CL at ge ea Liv d ec ad re NS HN ha Br r nc lo Bl op Co Pa Es Cancer cell

  8. Slide 8: Targeting IL1RAP provides unique opportunities to treat cancer by IL-1α/β blockade and ADCC

    Targeting IL1RAP provides unique opportunities to treat cancer by IL-1α/β blockade and ADCC Nadunolimab NADUNOLIMAB COUNTERACTS IMMUNE SUPPRESSION AND POTENTIATES THERAPY ADCC – Antibody-Dependent Cellular Cytotoxicity; TIR – Toll-Interleukin-1 Receptor; NK – Natural Killer 8

  9. Slide 9: Nadunolimab potentiates antitumor activity of chemotherapy

    Nadunolimab potentiates antitumor activity of chemo- therapy Nadunolimab IL-1α Tumor growth * 20 100 Relative expression Tumor volume (%) 15 ** Control Docetaxel 10 50 Anti-IL-1β + Docetaxel Nadunolimab + Docetaxel 5 0 0 4 500 Docetaxel (nM) → Nadunolimab blocks both IL-1α and → Docetaxel induces IL

  10. Slide 10: Chemotherapy induces IL-1α and IL-1β in the tumor

    Chemotherapy induces IL-1α and IL-1β in the tumor IL-1α IL-1β-converting enzyme Tumor cell region (T) Stromal cell region (S) 6 * Control Gem/Cis 250 ** Control Gem/Cis 2 Positive cells/mm % Positive cells S 200 T T 4 T 150 S S 100 2 S T T 50 T 0 0 l s t ro Ci is l / ro n /C Co Gem nt m Co Ge → Gem/

  11. Slide 11: Targeting IL1RAP uniquely synergizes with chemotherapy

    Targeting IL1RAP uniquely synergizes with chemotherapy Tumor growth Body weight 2000 0 Tumor volume (mm ) 3 1500 Vehicle % Change Iso Control -5 Vehicle 1000 Nadunolimab Gem/Cis Gem/Cis ** Nadunolimab+Gem/Cis Nadunolimab+Gem/Cis -10 500 * 0 -15 0 5 10 15 Day post-treatment → Nadunolimab increases ef

  12. Slide 12: Induction of IL1RAP and IL-1α with therapy in NSCLC pts

    Induction of IL1RAP and IL-1α with therapy in NSCLC pts Pre-treatment On treatment (Nadunolimab + Gem/Cis) IL1RAP (brown) IL-1α (brown) IL-1ALPHA INDUCED BY CHEMOTHERAPY IN LINE WITH PRECLINICAL FINDINGS; WELL ESTABLISHED DANGER SIGNAL – ACTIVITY BLOCKED BY NADUNOLIMAB 12

  13. Slide 13: PDAC staging and treatment

    PDAC staging and treatment Expected number of cases US 2023: 64,000 Stage I - local: 3,200 Stage II - regional LN: 3,200 Stage IV - Stage III - metastatic: locally adv: 32,000 25,600 Stage I Stage II Stage III Stage IV RESECTABLE OR BORDERLINE RESECTABLE DISEASE LOCALLY ADVANCED OR METASTATIC DISEAS

  14. Slide 14: Positive interim data in 1st line pancreatic cancer

    Positive interim data in 1st line pancreatic cancer Nadunolimab combination 50% Best change in tumor size with Gem/Abraxane in 1st line PDAC (n=73): 0% → 33% response rate with long PFS and OS -50% → Additional 5 (7%) pts had on- treatment benefit beyond progression -100% iCPD iUPD iSD iPR → Promisi

  15. Slide 15: Strong efficacy in PDAC pts with high tumor IL1RAP levels

    Strong efficacy in PDAC pts with high tumor IL1RAP levels IL1RAP High IL1RAP Low 50% Best change in tumor size iCPD 0% iUPD iSD iPR -50% -100% Efficacy analysis for IL1RAP High (n=27) vs IL1RAP Low (n=19) PDAC pts: → Significantly prolonged OS in ILRAP High vs IL1RAP Low pts (14.2 vs 10.6 months; p=

  16. Slide 16: PDAC pts with high tumor IL1RAP levels have the strongest benefit of nadunolimab combination therapy

       OS    Nadunolimab/GN IL1RAP High PDAC pts with high tumor IL1RAP levels have the strongest   OS  Nadunolimab monotherapy Death  On study   benefit of nadunolimab combination therapy  Nadunolimab/GN iUPD/iCPD IL1RAP High  Nadunolimab monotherapy iSD Death iPR   On study iUPD/iCPD i

  17. Slide 17: Safety profile is manageable and supports MOA

    Safety profile is manageable and supports MOA → Neutropenia manageable through G-CSF prophylaxis → In 7 pts given G-CSF prophylaxis, only 1 developed grade 3-4 neutropenia All Patients in All Cycles → Only 1 % peripheral neuropathy grade 3-4 observed (17% in historical controls) 100% n=6 n=15 Grade

  18. Slide 18: Updated efficacy in NSCLC to be presented at ASCO 2023

    Updated efficacy in NSCLC to be presented at ASCO 2023 Nadunolimab combination with Gem/Cis in 1st/2nd line NSCLC: Non- → 16 of 30 pts with objective response incl. 2 Non- complete responses All Historical squamous, squamous (n=30) control1,2 historical → One CR achieved on nadunolimab monotherapy (

  19. Slide 19: Promising early safety and efficacy in TNBC

    Promising early safety and efficacy in TNBC Nadunolimab combination with Gem/Carbo in 100 % 1st/2nd line metastatic TNBC: Best change in tumor size 15 pts enrolled in the dose-escalation phase 50 % PD → Acceptable safety profile (G-CSF given prophylactically to control neutropenia) SD 0% → 12 pts tr

  20. Slide 20: Key messages

    Key messages → Most chemotherapies induce chemoresistance already after Resistant a few months of therapy. Chemotherapy can upregulate tumor both IL-1α and IL-1β. Chemo- therapy → Unlike other IL-1 blocking compounds, nadunolimab blocks both IL-1α and IL-1β signalling and improves chemotherapy effic

  21. Slide 21: CAN10 – Opportunity in Autoimmune/Inflammatory Disease

    CAN10 – OPPORTUNITY IN AUTOIMMUNE/INFLAMMATORY DISEASE

  22. Slide 22: CAN10 – New asset within autoimmunity/inflammation

    CAN10 – New asset within autoimmunity/inflammation → IL1RAP-binding antibody potently blocking IL-1, IL-33 and IL-36, without ADCC → Unique anti-inflammatory activity observed in different mouse models (myocarditis, systemic sclerosis, psoriasis, inflammation) → Development focusing on systemic scle

  23. Slide 23: CAN10 – Promising effects in several preclinical disease models

    CAN10 – Promising effects in several preclinical disease models Viral myocarditis Disease severity Autoimmune myocarditis Cardiac function 4 *** 1.1 Ratio to baseline * ** 3 1.0 * mCAN10 Ctrl mCAN10 Score 2 0.9 Anti-IL-1β Ctrl Anti-IL-1β Vehicle 1 0.8 0 0.7 0 10 20 30 40 cle A l 0 ro 1R N1 Day nt hi

  24. Slide 24: CAN10 – Project status

    CAN10 – Project status GLP toxicity study – Completed → CAN10 given i.v. once weekly for six weeks at doses up to 50 mg/kg or s.c. at 5 mg/kg → No adverse findings related to CAN10 at/above clinically relevant (pharmacologically active) dose levels Clinical phase I trial – Study start planned for mi

  25. Slide 25: Financials, Milestones & Summary

    FINANCIALS, MILESTONES & SUMMARY

  26. Slide 26: Planned next steps

    Planned next steps Nadunolimab PDAC NSCLC TNBC CAN10 • Start phase IIb clinical • Evaluate biomarkers in • Randomized phase II • Treatment of first trial in 150-200 pts with 40+ pts treated with stage in TRIFOUR: subject in phase I submssion H2 2023, nadunolimab+chemo to Interim futility analysis cl

  27. Slide 27: Several upcoming value inflection points

    Several upcoming value inflection points Newsflow over next quarters Nadunolimab (CAN04) → Update of results for PDAC, NSCLC and TNBC → Start phase IIb trial in PDAC → New preclinical and translational results → New clinical data (efficacy and safety) → CAPAFOUR PDAC FOLFIRINOX → CESTAFOUR Basket tr

  28. Slide 28: Solid financial position with strong shareholder support

    Solid financial position with strong shareholder support → Cash and cash equivalents 353 MSEK (~$33M) at end of Q1 2023 Current owners (Mar 31, 2023) → Runway until mid-2024 4th AP fund 8.8% Alecta 7.3% → Market cap approx. 0.8 BSEK, 75 MUSD May 26, 2023 1st AP fund 6.3% Avanza Pension 5.1% Six Sis

  29. Slide 29: Cantargia: Investment highlights

    Cantargia: Investment highlights NOVEL IL1RAP ANTIBODIES, POTENTIAL TO ADDRESS CANCER & INFLAMMATORY DISEASE • IL1RAP elevated in most solid and liquid tumors • Potential to breakdown resistance to cancer treatment, enabled by unique dual action approach – nadunolimab • Additional key target for inf

Cantargia — Investor Presentation (May 2023) on 6ix