Sernova Biotherapeutics Inc · TSX:SVA

Sernova Biotherapeutics — Merger or Acquisition (2026)

16 slides from Sernova Biotherapeutics's merger presentation, 2026

  1. Slide 1: Sernova (SVA.TO) & Seraxis Merge to Form

    Sernova (SVA.TO) & Seraxis Merge to Form; Integrating Science. Working with Passion. Developing a Functional Cure for T1D.* Non-Con Q3 2026

  2. Slide 2: Disclaimers and Forward-Looking Statements

    DISCLAIMERS AND FORWARD-LOOKING STATEMENTS MUST READ This presentation is confidential and for your information only and is not intended to be distributed to or reviewed by anyone other than you. This presentation has been prepared by Sernova and is being supplied to you on a confidential basis for

  3. Slide 3: Merger aims to create a differentiated approach to T1D cell therapy

    MERGER AIMS TO CREATE A DIFFERENTIATED APPROACH TO T1D CELL THERAPY OUR MISSION: UPCOMIMG MILESTONES Working toward a potential functional cure for Type 1 Diabetes by uniting: • Merger agreement executed 1. Stem Cell–Derived Islets • Closing in November • SR-02, allogeneic insulin producing cells (I

  4. Slide 4: What is the problem?

    WHAT IS THE PROBLEM? Pump and CGN 3 Diabetic retinopathy Brain stroke Cerebrovascular Cataracts disease Glaucoma Donor Islet Transplant Cardiovascular Periodontal disease disease Published research indicates roughly 1 in 10 people with T1D die of severe hypoglycemia¹ Diabetic Peripheral nephropathy

  5. Slide 5: Advantages of Betanova SR-02 & SR-03 stem cells

    ADVANTAGES OF BETANOVA SR-02 & SR-03 STEM CELLS A HUMAN PANCREAS-DERIVED CELL LINE FOR ISLET MANUFACTURING Potent Islet Cells • In vitro tests show high insulin secretion and glucose responsiveness Developed For Organ Transplant Compatibility • Blood type 0, Rh negative, common HLA profile Streamlin

  6. Slide 6: Betanova SR-02

    BETANOVA SR-02 THIRD PARTY ASSESSMENT OF GLUCOSE RESPONSIVENESS (Data on File) • Stimulation of SR-02 beta cells with glucose induced biphasic influx of calcium that correlated with insulin secretion • Independent testing showed glucose- linked calcium influx & insulin secretion. • Potency similar t

  7. Slide 7: SR-02 pre-clinical cell validation

    SR-02 PRE-CLINICAL CELL VALIDATION PRECLINICAL ANIMAL DATA Nonfasting blood glucose by site and dose Nonfasting immunocompromised mice Blood Glucose By Site and Dose Immunocompromised Mice Fat pad, 5,000 iEQ (n=6) Fat pad, 2,500 iEQ (n=11) Manufactured Islets 600 Low Magnification Blood glucose (mg/

  8. Slide 8: Reducing immune suppression

    REDUCING IMMUNE SUPPRESSION (Investigational) Strategy #1 (IND cleared by FDA to begin study) HLA1 • Use modern immune-suppression to minimize Rationale burden, promote maximum tolerance Beta cells • Co-stimulatory blockers or others • Strong clinical evidence (SR-02) in Co-stimulatory blockers • We

  9. Slide 9: SR-03 immune evading cells

    SR-03 IMMUNE EVADING CELLS SR-03 IS GENE-EDITED TO AVOID IMMUNE TARGETING SR-02 • Loss-of-function strategy eliminates determinants of - IgG IgM Nucleus organ rejection while maintaining long-term durability - Antibodies formed against cells NO DETECTABLE ANTIBODIES OBSERVED • Rodents with humanized

  10. Slide 10: Manufacturing: SR-02 & SR-03 allogeneic stem cell line

    MANUFACTURING: SR-02 & SR-03 ALLOGENEIC STEM CELL LINE HIGH-PURITY, HIGH-POTENCY ISLETS (Preclinical) MANUFACTURING - No sorting or selection required to achieve high purity - High-compatibility, single-donor source - Hundreds of manufacturing runs completed - Type O, Rh- with common HLA profile - D

  11. Slide 11: Completed Phase 1/2 Cell Pouch cadaveric cell clinical trial

    COMPLETED - PHASE 1 / 2 CELL POUCH CADAVERIC CELL CLINICAL TRIAL Overall Objectives ▪ Demonstrate safety & tolerability of Cell Pouch/Human PRIMARY AND SECONDARY Donor Islet transplantation ENDPOINTS MET (SEE NCT03513939) ▪ Define islet release criteria predictive of clinical outcomes ▪ Establish op

  12. Slide 12: Betanova Cell Pouch bio-hybrid organ

    BETANOVA CELL POUCH BIO-HYBRID ORGAN CELL POUCH PRE-IMPLANT BIO – HYBRID ORGAN POST REMOVAL Phase 1/2 Findings on Safety and Function (Investigational) Phase 1/ 2 clinical trial for Type 1 Diabetes complete Vascularized Tissue Environment Designed to remodel the implant site into a vascularized tiss

  13. Slide 13: Phase 1/2 trial - insulin-producing beta cells throughout Cell Pouch after 5 years

    PHASE 1/ 2 TRIAL - ABUNDANT, VASCULARIZED, INSULIN-PRODUCING BETA CELLS THROUGHOUT CELL POUCH AFTER 5-YEARS 8 CHANNEL CELL POUCH TISSUE CHAMBERS: 1 2 3 4 5 6 7 8 INS vWF ▪ Positive immunofluorescent staining for Insulin, and Von Willebrand Factor (blood vessels), Glucagon & Somatostatin ▪ Rich vascu

  14. Slide 14: FDA position on retrievability and containment for stem cell-derived islet therapy

    FDA POSITION ON RETRIEVABILITY AND CONTAINMENT FOR STEM CELL- DERIVED ISLET THERAPY • FDA guidance ; a retrieval mechanism is preferable for stem cell-derived islet therapies¹·²·⁴ • Company believes a retrievable device is more likely to be required as a safety requirement • Stem cell-derived and ge

  15. Slide 15: Patient willingness to adopt cell-based therapies for T1D

    PATIENT WILLINGNESS TO ADOPT CELL-BASED THERAPIES FOR T1D IS OVERWHELMING | 2017 Survey across North America, Europe, and Asia found 72% interested in participating in clinical trials for bio-artificial pancreas systems, (Diabetes Technology & Therapeutics, 2017). | 2019 Study found ~75% expressed i

  16. Slide 16: Thank You

    Thank You Inquiries? Contact: David Burke, V.P. Investor Relations David.Burke@Sernova.com

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