Maat Pharma · EURONEXT:MAAT

Maat Pharma — Investor Presentation (April 2025)

32 slides from Maat Pharma's investor presentation, April 2025

  1. Slide 1: Boosting Survival Through Innovative Immune Modulation

    Boosting Survival Through Innovative Immune Modulation April 2025

  2. Slide 2: Disclaimer

    MaaT Pharma April 2025 2 Disclaimer This document has been prepared by MaaT Pharma (the "Company") The information contained in this document has not been subject to This document contains certain forward-looking statements. These and is for information and background purposes only. independent veri

  3. Slide 3: Management Team

    MaaT Pharma April 2025 3 Management Team Hervé Affagard Eric Soyer Gianfranco Pittari, Carole Jonathan Chriqui, MD, PhD Schwintner, PhD PharmD Co-Founder & CEO Chief Financial Chief Medical Chief Technology Chief Business Officer Officer Officer Officer

  4. Slide 4: Company Overview

    Company Overview

  5. Slide 5: MaaT013 in aGvHD: Achieved Primary Endpoint of Phase 3 Study

    MaaT Pharma April 2025 5 MaaT013 in aGvHD: Achieved Primary Endpoint of Phase 3 Study Registration in Europe Will Spearhead Microbiome Therapies in Oncology Now available: Phase 3 Data in Multi-assets platform Funding aGvHD from the ARES study focused on oncology opportunities Primary endpoint: unpr

  6. Slide 6: Correcting Dysbiosis: a New Pillar in Oncology

    MaaT Pharma April 2025 6 Correcting Dysbiosis: a New Pillar in Oncology Dysbiosis and disease • Loss of microbial diversity • Increase in pathogens • Reduction of microbial metabolites • Associated with multiple conditions Microbiotherapy Restores Gut Microbiota Diversity and Production of Microbiom

  7. Slide 7: Oncology-Focused Platform Fueling a Deep Pipeline of Drug Candidates

    MaaT Pharma April 2025 7 Oncology-Focused Platform Fueling a Deep Pipeline of Drug Candidates Native Ecosystem Co-cultured Ecosystem In-house Production Driving near-term value Progressing next-generation Leading capabilities in full ecosystem with the donor-derived MET-N platform co-cultured scalab

  8. Slide 8: A Strong Pipeline With Multiple Value Inflection Milestones and a Close-to-Market Asset

    MaaT Pharma April 2025 8 A Strong Pipeline With Multiple Value Inflection Milestones and a Close-to-Market Asset Program Indication Market potential Preclinical Phase 1 Phase 2 Phase 3 MAA Status Upcoming milestone Primary EU MAA Submission ARES MaaT013 1L : 10k patients2 endpoint met June 2025 2L :

  9. Slide 9: Leveraging Microbiome Modulation in Oncology: Mechanisms for Enhanced Survival Outcomes

    MaaT Pharma April 2025 9 Leveraging Microbiome Modulation in Oncology: Mechanisms for Enhanced Survival Outcomes in Multiple Settings Control of inflammation and restoration of gut integrity and production of functional metabolites Resolution • Immune modulation curbing inflammatory response Restora

  10. Slide 10: MaaT013 in aGvHD

    MaaT013 in aGvHD

  11. Slide 11: Understanding and Addressing Acute Graft-versus-Host Disease (aGvHD)

    MaaT013 • aGvHD → Salvage ODD EMA/FDA MaaT Pharma → Quick action April 2025 11 Understanding and Addressing Acute Graft-versus-Host Disease (aGvHD) → A significant complication following allogeneic hematopoietic stem cell transplantation (Allo-HSCT) → May occur in 50% of patients undergoing Allo-HSC

  12. Slide 12: aGvHD Refractory to Steroids and Ruxolitinib: A Substantial Unmet Medical Need

    MaaT013 • aGvHD → Salvage ODD EMA/FDA MaaT Pharma → Quick action April 2025 12 ODD EMA/FDA aGvHD Refractory to Steroids and Ruxolitinib (3rd line treatment): A Substantial Unmet Medical Need Requiring Innovative Solutions Treatment Paradigm Lack of effective therapy in 3rd line Corticosteroids are t

  13. Slide 13: ARES: a Pivotal Phase 3 Trial Exploring MaaT013 in 3rd-Line aGvHD

    MaaT013 • aGvHD → Salvage ODD EMA/FDA → Quick action MaaT Pharma April 2025 13 ARES: a Pivotal Phase 3 Trial Exploring MaaT013 in 3rd-Line aGvHD Following Steroid and Ruxolitinib Failure Milestones: Topline results announced January 8th 2025 I OS expected by end of 2025 I Regulatory submission expec

  14. Slide 14: ARES patients: Baseline Characteristics

    MaaT013 • aGvHD → Salvage ODD EMA/FDA MaaT Pharma → Quick action April 2025 14 ARES patients: Baseline Characteristics Patients characteristics at baseline All patients receiving MaaT013 (n=66) Median age, years (range) 55.5 (24; 76) Gender n (%) Male: 35 (53%) Female: 31 (47%) Steroid status n (%)

  15. Slide 15: ARES: Strong Response to MaaT013 in aGvHD Following Steroid and Ruxolitinib Failure

    MaaT013 • aGvHD → Salvage ODD EMA/FDA MaaT Pharma → Quick action April 2025 15 ARES: Strong Response to MaaT013 in aGvHD Following Steroid and Ruxolitinib Failure D28 Response Rate (%) Topline Results “ These outcomes underscore the curative role of microbiota- 80 80 based therapies in achieving 95%

  16. Slide 16: ARES: Unprecedented Probability of Survival Compared to Historical Data with BAT

    MaaT013 • aGvHD → Salvage ODD EMA/FDA MaaT Pharma → Quick action April 2025 16 ARES: Unprecedented Probability of Survival Compared to Historical Data with Best Available Therapy (BAT) Overall Survival, ARES vs BAT Probability of Survival by D28 Response Probability of Survival (%) Probability of Su

  17. Slide 17: Early Access Program: meeting critical needs in GvHD today and shaping the future

    MaaT013 • aGvHD → Salvage ODD EMA/FDA MaaT Pharma → Quick action April 2025 17 Early Access Program: meeting critical needs in GvHD today and shaping the future 1 2 3 4 Patients First Supplying The Increasing In Different Indications Clinical Value Number International Demand of patients 154 cumulat

  18. Slide 18: Regulatory Path for MaaT013 in Third-Line Refractory aGvHD

    MaaT013 • aGvHD → Salvage ODD EMA/FDA MaaT Pharma → Quick action April 2025 18 Regulatory Path for MaaT013 in Third-Line Refractory aGvHD: Established in Europe, Leveraging EU Results for Ongoing US Discussions In Europe In the U.S. Eligibility of MaaT013 for the centralized procedure Open IND: Ongo

  19. Slide 19: A Multi-Asset Platform Focused on Oncology

    A Multi-Asset Platform Focused on Oncology

  20. Slide 20: Phoebus: MaaT033 Phase 2b RCT

    → Ambulatory MaaT033 • Allo-HSCT MaaT Pharma → Adjunctive April 2025 20 Phoebus: MaaT033 Phase 2b RCT Potential Adjunctive Treatment for Patients Receiving Allo-HSCT Visit 1 Visit 2 15 – 21 days Visit 3 Visit 6 Visit 10 D-21 D-7 D-0 Neutrophil recovery D+21 M+3 M+12 Pre Allo-HSCT Post Allo-HSCT trea

  21. Slide 21: Unlocking the Potential of Checkpoint Inhibitors

    → ICI MaaT013 • IO - Melanoma MaaT Pharma → Combo April 2025 21 Unlocking the Potential of Checkpoint Inhibitors: How Full-Ecosystem Gut Microbiome Overcomes Primary Resistance Immune Checkpoint Inhibitors (ICI) significantly Leveraging full ecosystem microbiome improve outcomes in solid tumor patie

  22. Slide 22: MaaT013 Evaluated in Phase 2 Randomized, Multicenter Clinical Trial in Melanoma

    → ICI MaaT013 • IO - Melanoma MaaT Pharma → Combo April 2025 22 MaaT013 Evaluated in Phase 2 Randomized, Multicenter Clinical Trial in Melanoma Phase 2a PICASSO trial, fully recruited Key study endpoints after 23 weeks of treatment: Investigator Sponsored Trial (Assistance Publique - Hôpitaux de Par

  23. Slide 23: MaaT033: Targeting Amyotrophic Lateral Sclerosis Progression

    MaaT033 • ALS → Ambulatory MaaT Pharma April 2025 23 MaaT033: Targeting Amyotrophic Lateral Sclerosis Progression Amyotrophic Lateral Sclerosis (ALS) Rationale for Exploratory Utilization of MaaT033 in ALS → Could affect up to 60,000 patients in US & EU by 2040 1 → Microbiota-Gut-Brain axis is a mul

  24. Slide 24: MET-C Product Generation Driven by Proprietary Predictive AI

    → Synthetic MET-C • ICI and more → Tailored MaaT Pharma April 2025 24 MET-C Product Generation is Driven by MaaT Pharma’s Proprietary Predictive AI, Eubiotic Score and in vitro and in vivo Validation Processes MaaT034 MaaT034 In silico In vitro In vivo Clinic Candidate Products Upcoming Milestones I

  25. Slide 25: Hemato-oncology Franchise Driving Value

    Hemato- oncology Franchise Driving Value

  26. Slide 26: MaaT013: High-Margin Potential and Addressable Market Opportunity

    → Salvage MaaT013 • aGvHD → Quick action MaaT Pharma April 2025 26 MaaT013: High-Margin Potential and Addressable Market Opportunity Addressable market in 3L* Estimated Annual Revenues ~3,000 patients 65% Market penetration 3L GI-SR-RR/I-aGvHD 3L GI-SR-RR/I-aGvHD (~2,000 patients) • Ruxolitinib: ~70

  27. Slide 27: Realizing Value through Partnership in Hematology

    MaaT Pharma April 2025 27 Realizing Value through Partnership: Aligning Innovation with Unmet Medical Needs in Hematology Unique Franchise Opportunity A very meaningful market opportunity Unique immunosuppressant-sparing, microbiome-based approach Well defined target population for both products, Pr

  28. Slide 28: End-to-End In-house cGMP Manufacturing Capabilities

    End-to-End In-house cGMP Manufacturing Capabilities

  29. Slide 29: Europe's Largest Specialized cGMP Manufacturing Facility for Microbiome Ecosystem Therapies

    → cGMP All MET → Scalable MaaT Pharma April 2025 29 01 Europe’s Largest Leading microbiome therapies fully integrated Specialized cGMP manufacturing and development platform: streamlined product development, scaleup and GMP Manufacturing process. Facility for Microbiome Ecosystem Therapies 02 Option

  30. Slide 30: Newsflow & Funding Opportunities

    Newsflow & Funding Opportunities

  31. Slide 31: Several Major Near-Term Value Inflection Expected Milestones

    MaaT Pharma April 2025 31 Several Major Near-Term Value Inflection Expected Milestones 2025 2026 2027 MaaT013 GvHD | Ares Ph3 28 days GI-ORR results Jan 25 MaaT013 GvHD | MA application EMA June 25 MaaT013 MaaT013 Hemato GvHD | Ares Ph3 OS results H2 25 GvHD | MA approval EMA H2 26 - MaaT013 MaaT013

  32. Slide 32: Thank you

    Thank you _ * 9@,S@ x rae nar,

MaaT Pharma — Investor Presentation (April 2025) on 6ix