Cantargia Ab · OMXSTO:CANTA

Cantargia Ab — Q1 2024 Earnings Presentation

24 slides from Cantargia Ab's earnings presentation, May 21, 2024

  1. Slide 1: Q1 Report May 21, 2024

    (oantargia Q1 REPORT May 21, 2024

  2. Slide 2: Safe Harbour Statement

    Safe Harbour 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 an

  3. Slide 3: Significant events

    Significant events… … in Quarter 1: • The first results from the ongoing clinical phase 1 study of CAN10 show that the antibody binds to the target IL1RAP and shows good safety. The study is progressing according to plan. • New clinical and preclinical results show that nadunolimab can reduce neurop

  4. Slide 4: I. Project Status

    I. PROJECT STATUS

  5. Slide 5: Current pipeline

    Current pipeline Project Disease Type of Discovery Preclinical — Clinical Clinical Clinical ' treatment phase phase phase | phase II phase Ill PDAC 1% line Gemcitabine/nab-paclitaxel Nadunolimab TNBC 15*/2"4 jine Carboplatin/gemcitabine NSCLC/ ' non-squamous NSCLC ine Platinum doublets Systeme se TT

  6. Slide 6: Cantargia in 2024/25

    Cantargia in 2024/25 • Data from the two clinical programs • Several clinical milestones during 2024 and 2025 • Publications and conference presentations • Nadunolimab: Presentations at both AACR and ASCO • CAN10: Three publications in impactful journals and presentation at one conference INCREASED

  7. Slide 7: CAN10

    CAN10

  8. Slide 8: CAN10 - Targeting IL-1 family in inflammation

    CAN10 - Targeting IL-1 family in inflammation • Evidence of IL-1 family cytokines (IL-1, IL-33, IL-36) driving inflammatory diseases • These cytokines are commonly upregulated and operate together in several diseases • Blockade of individual IL-1 family members insufficient • IL-1 and IL-36 targeti

  9. Slide 9: CAN10 developed to block IL-1 family with precision

    CAN10 developed to block IL-1 family with precision • CAN10 prevents signaling from IL1/, IL-33 and IL36// • CAN10 binds IL1RAP with pM affinity and prevents IL1RAP interaction with the IL-1, IL-33 and IL-36 receptors • CAN10 has shown robust efficacy in preclinical models of several diseases •

  10. Slide 10: CAN10 first-in-human study ongoing

    CAN10 first-in-human study ongoing Rational for psoriasis in MAD • IV administration in healthy volunteers (SAD) • Ongoing, receptor occupancy documented • No safety signals • SC administration in subjects with mild to moderate plaque psoriasis (MAD) • Strong rational for IL1RAP blockade in psoriasi

  11. Slide 11: IL-1, IL-33 and IL-36 promote fibrosis in SSc fibroblasts

    IL-1, IL-33 and IL-36 directly promotes fibrosis in SSc fibroblasts which can be counteracted by CAN10 Isotype CAN10 Collagen I SMA Collagen I staining ✱ ✱✱✱✱ ✱✱✱✱ ✱ ✱✱ 1.6 ### #### 2.0 ✱✱ #### # ## #### Fold changes #### Fold changes 1.5 1.2 1.0 0.8 0.5 0.4 0.0 0.0 DPBS TGF ILs$ ILs$ DPBS TGF IL

  12. Slide 12: Systemic sclerosis: mCAN10 inhibits bleomycin-induced skin fibrosis

    Systemic sclerosis: mCAN10 inhibits bleomycin- induced skin fibrosis Bleomycin (BLM) model mCAN10 10 mg/kg twice W BLM 2.5 mg/kg (daily s.c.) Nintedanib 50 mg/kg QD C57BL/6 Established fibrosis Termination n=10 per group Week 3 Week 6 No BLM (6 wks) Baseline BLM (3 wks) Dermal thickness Myofibroblas

  13. Slide 13: Nadunolimab

    NADUNOLIMAB

  14. Slide 14: Nadunolimab and alleviation of neuropathy

    Nadunolimab and alleviation of neuropathy → Chemotherapy induce neuropathy by several pathways including IL-1 (neuroinflammation) → Nadunolimab, phase 2 data in PDAC with Gem/nabP → lower Grade 3-4 peripheral neuropathy than expected from historical controls (1% vs 17%). → Further analysis from this

  15. Slide 15: PDAC – Positive interim data in 1st line patients

    PDAC – Positive interim data in 1st line patients OS and iPFS for mITT patients Best responses according to iRECIST 50% Best change in tumor size 0% -50% -100% iCPD iUPD iSD iPR Nadunolimab combination with Gem/Abraxane in 1st line PDAC (n=73): → 33% response rate with long OS and iPFS → Additional

  16. Slide 16: 1st line PDAC – Strong efficacy in patients with high tumor IL1RAP

    1st line PDAC – Strong efficacy in patients with high tumor IL1RAP level OS by IL1RAP subgroup IL1RAP High IL1RAP Low 50% Best change in tumor size iCPD 0% iUPD iSD iPR -50% -100% Efficacy analysis for IL1RAP High (n=29) vs IL1RAP Low (n=20) PDAC patients (1st line, combination with Gem/Abraxane): →

  17. Slide 17: TNBC – Promising early safety and efficacy

    TNBC – Promising early safety and efficacy (1st/2nd line) Nadunolimab combination with Gem/Carbo in 1st/2nd line metastatic Best responses according to RECIST OS and PFS TNBC: 100% Best change in tumor size 15 patients enrolled in the dose- 50% escalation phase: → Preliminary ORR: 60% 0% (1 CR, 8 PR

  18. Slide 18: Nadunolimab in 2024/25

    Nadunolimab in 2024/25 • One randomized phase 2 clinical trial ongoing in TNBC • Two clinical trials to start (PDAC and AML/MDS) • A large number of precinical, translational and clinical results being analyzed • New data at ASCO 2024. SEVERALUPCOMING VALUE INFLECTION POINTS FOR NADUNOLIMAB 18

  19. Slide 19: Cantargia IP

    Cantargia IP → Lead candidate anti-IL1RAP antibody CAN04 Expiry year 2035 Granted (e.g. Europe, USA, China, Japan) Mother patent and divisionals → Lead candidate anti-IL1RAP antibody CAN10 Expiry year 2041 Granted (USA) Examination at early stage in remaining territories → Anti-IL1RAP for treatment

  20. Slide 20: II. Finance

    II. FINANCE

  21. Slide 21: Financial highlights

    Financial highlights Operating Expenses 78 5 -46% • Operating expenses decreased year over year by 46% to 42 (78) MSEK. 42 • R&D expenses amounted to 38 (73) MSEK. According to plan and due MSEK 3 to only two clinical trials (TRIFOUR and CAN10 phase 1) actively 73 recruiting, as well as no major inv

  22. Slide 22: Available funds

    Available funds MSEK 353 287 155 159 200 195 143 120 140 • Available funds decreased by 52 MSEK in the 197 108 quarter, from 195 to 143 (353) MSEK. 128 80 • The current available funds enable a runway of 12 55 35 months. 2023-03-31 2023-06-30 2023-09-30 2023-12-31 2024-03-31 Cash and bank balances S

  23. Slide 23: II. News Flow and Q&A

    II. NEWS FLOW AND Q&A

  24. Slide 24: Upcoming milestones

    Upcoming milestones Nadunolimab Additional PDAC TNBC AML/MDS CAN10 milestones • Presentation at ASCO • Full recruitment H2 •Start phase I/II mid • Phase I data updates • NSCLC – Efficacy & on neuropathy 2024 2024 (DOD sponsored during 2024 (including biomarker data from • Start of Phase IIb trial •R

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