Scinai Immunotherapeutics Ltd. · NASDAQ:SCNI

Scinai Immunotherapeutics — Investor Presentation (June 2024)

44 slides from Scinai Immunotherapeutics's investor presentation, Jun 14, 2024

  1. Slide 1: Corporate Presentation June 2024

    CLICK TO EDIT MASTER TITLE STYLE CORPORATE PRESENTATION | JUNE 2024 | NASDAQ: SCNI NON - CONFIDENTIAL PUBLIC INFORMATION

  2. Slide 2: Safe Harbor Statement

    CLICK TO EDIT MASTER TITLE STYLE 2 SAFE HARBOR STATEMENT This communication contains forward - looking statements within the meaning of the Private Litigation Reform Act of 1995 . Words such as “expect,” “believe,” “intend,” “plan,” “continue,” “may,” “will,” “anticipate,” and similar expressions ar

  3. Slide 3: 2024: Building on 2023's Momentum

    CLICK TO EDIT MASTER TITLE STYLE 3 2024: BUILDING ON 2023’S MOMENTUM 2023 2024 BUSINESS DEVELOPMENT • Launched Scinai Bioservices CDMO • Capital infusions • New name, new brand • More CDMO clients • Pursue partnerships PIPELINE DEVELOPMENT • Licensed anti - IL - 17 NanoAb • Completed ex - vivo study

  4. Slide 4: Two Complementary Business Units

    CLICK TO EDIT MASTER TITLE STYLE 4 TWO COMPLEMENTARY BUSINESS UNITS End - to - end boutique CDMO services to help bring products to market by leveraging Scinai’s GMP and non - GMP drug development and manufacturing capabilities Development of inflammation and immunology (I&I) biological therapeutic

  5. Slide 5: Nanosized Antibody Pipeline: Huge Opportunity

    CLICK TO EDIT MASTER TITLE STYLE 5 Alpaca - derived nanosized antibodies (NanoAbs) are also known as VHH antibodies or nanobodies 1 mAb therapeutic market size is ~ $205 billion 2 including Cosentyx for psoriasis $4.8 billion (2022) 3 NanoAbs: Human monoclonal antibody (mAb)’s biobetter 1. VHH antib

  6. Slide 6: The Max Planck Institute & UMG bring...

    CLICK TO EDIT MASTER TITLE STYLE 6 The Max Planck Institute & UMG 1 bring… • Recombinant protein drug development experience from lab to Phase 3 clinical trial • Manufacturing, quality, international regulatory experience • GMP biologics manufacturing facility • Best - in - class equipped labs • Top

  7. Slide 7: NanoAbs' unique attributes vs monoclonal antibodies

    CLICK TO EDIT MASTER TITLE STYLE 7 NanoAbs’ unique physicochemical attributes can generate multiple crucial advantages vs human monoclonal antibodies (mAbs) Manufacturing • 10 - times more active pharmaceutical ingredients (API) per gram of manufactured protein vs. mAbs • Faster and lower cost produ

  8. Slide 8: Derisked Drug Development

    CLICK TO EDIT MASTER TITLE STYLE 8 Source of Risk Molecular Target Mechanism of Action Composition of Matter TBD Commercial Validated by existing but sub - optimal mAb therapies Well understood Assessing safety & efficacy of alpaca - derived NanoAbs Strong demand for available mAbs and underserved p

  9. Slide 9: Superior Routes of Administration

    CLICK TO EDIT MASTER TITLE STYLE 9 SUPERIOR ROUTES OF ADMINISTRATION P aper covers several aspects of Scinai’s anti - COVID - 19 NanoAbs, including: • S tructure • Mechanism of action • Neutralization of a wide range of SARS - CoV - 2 variants including Omicron • Production in yeast • Formulation in

  10. Slide 10: Pipeline Molecular Targets

    CLICK TO EDIT MASTER TITLE STYLE 10 RBD IL - 4R α ANG - 2 IL - 17A/F • Strong in vivo data for inhaled therapeutic and prophylactic in a challenge study conducted with Fraunhofer ITEM and TiHO • Single compound targeting IL - 17A and IL - 17F and IL - 17AF • Novel local use • Larger target populatio

  11. Slide 11: Pipeline Addressing Large Markets with Underserved Needs

    CLICK TO EDIT MASTER TITLE STYLE 11 Psoriasis $17.4B Macular Degeneration (AMD) $6.9B Psoriatic arthritis $8.1B $10.4B Asthma Autoimmune Market Sizes • Validated targets of existing mAb treatments • Short time to value generation, lower risk than mAbs • Large markets growing at attractive CAGRs PIPE

  12. Slide 12: Pipeline Development: Status & Upcoming Milestones

    CLICK TO EDIT MASTER TITLE STYLE 12 PIPELINE DEVELOPMENT: STATUS & UPCOMING MILESTONES Anti - IL - 17 psoriasis treatment in - vivo proof - of - concept in 2024, clinical trial H1 2025 Clinical Phase 1/2 Toxicology In Vivo Proof - of - Concept In vitro / Ex vivo Manufacturing Process & Analytical Me

  13. Slide 13: Psoriasis: 78% Underserved Population

    CLICK TO EDIT MASTER TITLE STYLE 13 PSORIARIS: 78% UNDERSERVED POPULATION Psoriasis prevalence and severity SEVERE MODERATE MILD 22% of patients. 28% of patients. 50% of patients. >10% of the body Typically has a severe impact on quality of life 3 - 10% of the body Generally affects quality of life

  14. Slide 14: Current Plaque Psoriasis Treatments

    CLICK TO EDIT MASTER TITLE STYLE 14 CURRENT PLAQUE PSORIASIS TREATMENTS Corticosteroid creams, vitamin E+A, vitamin D derivatives Phototherapy 1 st line systemic immunosuppressants (Methotrexate and Cyclosporine) & Immunomodulators (Otezla) 2 nd line systemic Immunomodulators (e.g. Sotyktu ) Injecta

  15. Slide 15: NanoAbs Address Unmet Need

    CLICK TO EDIT MASTER TITLE STYLE 15 NANOABs ADDRESS UNMET NEED Designed to be convenient, safe, affordable, effective biologic for mild and moderate patients Current treatment shortcomings Corticosteroids • Side effects include: • Skin thinning (bruising) & Lightening of skin color • Development of

  16. Slide 16: Why do we need more?

    CLICK TO EDIT MASTER TITLE STYLE Why do we need more? ▪ Not all patients achieve complete clearance (PASI90 or PASI100) and some suffer from recalcitrant lesions that do not respond adequately ▪ Some patients have psoriasis in difficult - to - treat areas such as hands, feet, scalp, genitals... ▪ Ev

  17. Slide 17: Hard-to-treat lesions: scalp

    CLICK TO EDIT MASTER TITLE STYLE Hard - to - treat lesions: scalp pat . #1 pat . #2 pat . #3 Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony Institute of Occupational Dermatology, University Medical Center Göttingen, Germany https://hautklinik.umg.

  18. Slide 18: Hard-to-treat lesions: scalp

    CLICK TO EDIT MASTER TITLE STYLE pat . #4 pat . #5 Hard - to - treat lesions: scalp Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony Institute of Occupational Dermatology, University Medical Center Göttingen, Germany https://hautklinik.umg.eu

  19. Slide 19: Visible areas with high burden of disease: face

    CLICK TO EDIT MASTER TITLE STYLE Visible areas with high burden of disease: face pat . #6 pat . #7 pat . #8 pat . #9 Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony Institute of Occupational Dermatology, University Medical Center Göttingen, Germany

  20. Slide 20: Hard-to-treat lesions: hands

    CLICK TO EDIT MASTER TITLE STYLE Hard - to - treat lesions: hands pat . #10 pat . #11 Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony Institute of Occupational Dermatology, University Medical Center Göttingen, Germany https://hautklinik.umg.eu

  21. Slide 21: Sensitive areas: ano-genital region

    CLICK TO EDIT MASTER TITLE STYLE Sensitive areas with high burden of disease: ano - genital region pat . #9 pat . #12 Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony Institute of Occupational Dermatology, University Medical Center Göttingen, German

  22. Slide 22: Special locations: navel and nipples

    CLICK TO EDIT MASTER TITLE STYLE Special locations: navel and nipples image courtesy of Prof. D. Thaci, Lübeck pat . #13 pat . #14 Right nipple healthy Left nipple with psoriasis Navel with psoriasis Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony

  23. Slide 23: Recalcitrant isolated lesions

    CLICK TO EDIT MASTER TITLE STYLE Recalcitrant isolated lesions pat . #15 pat . #16 pat . #17 Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony Institute of Occupational Dermatology, University Medical Center Göttingen, Germany https://hautklinik.umg.

  24. Slide 24: Pretreated lesions with therapy side effects: soles

    CLICK TO EDIT MASTER TITLE STYLE Pretreated lesions with therapy side effects: soles pat . #18 pat . #19 After treatment with Corticosteroids Before treatment with Corticosteroids Credit: Prof. Michael P. Schön, Department of Dermatology, Venereology and Allergology Lower Saxony Institute of Occupat

  25. Slide 25: Why Develop an Anti-IL-17 NanoAb?

    CLICK TO EDIT MASTER TITLE STYLE 25 WHY DEVELOP AN ANTI - IL - 17 NANOAB? Rationale Success Factor IL - 17 as a molecular target in psoriasis is well understood and validated by existing therapies, e.g., Cosentyx, Siliq , Taltz and Bimzelx . IL - 17 is a well - established psoriasis target IL - 17 F

  26. Slide 26: Local ID injection of Anti-IL-17A/F VHH antibody fragment

    CLICK TO EDIT MASTER TITLE STYLE 26 Local ID injection of Anti - IL - 17A/F VHH antibody fragment  A novel way to using VHH antibodies - Most other entities working with VHHs (nanobodies®) aim to mimic mAbs “playbook” and hence are competing for the same patient populations and are using the same r

  27. Slide 27: The Product

    CLICK TO EDIT MASTER TITLE STYLE 27 The product An intradermal pen filled with a liquid formulation of Scinai’s anti - IL - 17A/F nanoAb given every 3 to 6 months at the doctor’s office. • Upon a patient’s visit, a pen injector with a sterile cartridge filled with 1.5 to 3ml of Scinai’s formulated n

  28. Slide 28: Generating incentives for the customers – the three P's

    CLICK TO EDIT MASTER TITLE STYLE 28 Generating incentives for the customers – the three P’s Patients: Mild to moderate plaque psoriasis patients. • Currently treated with corticosteroids and are unhappy : • Inconvenience of use (e.g. twice a day, use of ointments/creams). • Development of tolerance

  29. Slide 29: Where is the money?

    CLICK TO EDIT MASTER TITLE STYLE 29 Where is the money? • Total sales of drugs in the 7MM for mild psoriasis expected to be $1.8B in 2030 • $1.3B is expected to come from prescription of biologics and $259M from TYK2 inhibitor • This is the market where the topicals and phototherapy do not help. • T

  30. Slide 30: Anti-IL-17 NanoAb: A better neutralizer

    CLICK TO EDIT MASTER TITLE STYLE 30 Anti - IL - 17 Nanoab : A better neutralizer Single nanoAb neutralizes IL - 17 A, F, and AF complex 0.1 1 10 100 1000 10000 -0.2 0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 IL-17A Concentration (ng/mL) n o r m a l i z e d i n d u c t i o n a b o v e b a c k g r o u n d Re42B0

  31. Slide 31: Ex-vivo proof of concept: NanoAbs shown to block IL-17

    CLICK TO EDIT MASTER TITLE STYLE 31 EX - VIVO PROOF OF CONCEPT: NANOABS SHOWN TO BLOCK IL - 17 Impact of ID injected nanoAb in comparison to current leading treatments Betamethasone and Cosentyx Designed to be local, less frequent use, safer, more convenient and more affordable *** = p<0.001 **** =

  32. Slide 32: Limited systemic exposure expected

    CLICK TO EDIT MASTER TITLE STYLE 32 SCN - 1 is expected to show limited systemic exposure • Literature 1 indicates an estimated t1/2 in the blood following systemic injection of ~2 hrs ; • After ID - injection systemic exposure was less than 1.5% of administered drug after 2 hrs. 0 200 400 600 800 1

  33. Slide 33: In vivo PoC: Human xenograft skin (1/2)

    CLICK TO EDIT MASTER TITLE STYLE 33 In vivo PoC: Human xenograft skin (1/2) Animal model: Normal human skin engrafted into SCID BEIGE mouse and disease induced by injection of IL - 2 activated PBMCs from psoriatic patients Study design Study endpoints Follow up (3 weeks) Treatment (15 days) Psoriasi

  34. Slide 34: In vivo PoC: Human xenograft skin (2/2)

    CLICK TO EDIT MASTER TITLE STYLE 34 In vivo PoC: Human xenograft skin (2/2) What is being studied? The impact of local psoriasis treatments by efficacy parameters: x Clinical evaluation by medical photographs. x Macroscopic evaluation, epidermis thickness scoring & Histological analysis. x IHC analy

  35. Slide 35: Anti-IL-17 NanoAb program summary

    CLICK TO EDIT MASTER TITLE STYLE 35 IL - 17 nanoAb program summary • T here is a need for a better treatment for patients with mild to moderate Psoriasis and for specific lesions that are hard to treat with current therapies. • Biological drugs are the safest and most efficient, yet – they are admin

  36. Slide 36: IP Status Anti-IL-17 NanoAb

    CLICK TO EDIT MASTER TITLE STYLE 36 IP STATUS ANTI IL - 17 NANOAB Status • Priority patent application: Filed Dec. 28, 2022 • International patent application (PCT): Filed December 27, 2023 Covers • The patent application encompasses novel VHH antibodies directed against IL - 17 isomers and their us

  37. Slide 37: Boutique CDMO Services

    CLICK TO EDIT MASTER TITLE STYLE 37 BOUTIQUE CDMO SERVICES De - risking Scinai’s internal R&D investments by leveraging internal capabilities ASEPTIC GMP MANUFACTURING SUITES STATE - OF - THE - ART R & D AND QC LABORATORIES PHARMA CMC EXPERIENCE

  38. Slide 38: GMP Manufacturing and R&D Labs

    CLICK TO EDIT MASTER TITLE STYLE 38 GMP MANUFACTURING AND R&D LABS Industry standard aseptic facility: Labs, cleanroom, warehouses, offices • Analytical methods development combined with best - in - class QC capabilities and equipment • Labs for manufacturing process development and scale - up allow

  39. Slide 39: CDMO Strategic Guiding Principles

    CLICK TO EDIT MASTER TITLE STYLE 39 CDMO STRATEGIC GUIDING PRINCIPLES Scinai’s CDMO value proposition: Experienced and professional team available to execute drug development projects at high - speed while adhering to high (EU) quality standards using new and modern equipment located in a well - mai

  40. Slide 40: Deep Pharma Experience & Capabilities

    CLICK TO EDIT MASTER TITLE STYLE 40 DEEP PHARMA EXPERIENCE & CAPABILITIES AMIR REICHMAN – CEO Senior global pharma leadership positions: Pharmaceutical engineering & supply chain at GSK Vaccines, Belgium; Large projects building vaccine manufacturing sites in Belgium, Italy, Germany, Hungary & US; N

  41. Slide 41: Select Financials & Cap Table

    CLICK TO EDIT MASTER TITLE STYLE 41 SELECT FINANCIALS & CAP TABLE • $ 5 M cash as of March 31 , 2024 • € 24 M European Investment Bank (EIB) loan payable Dec 31 , 2031 Nasdaq: SCNI 723,812 ORDINARY ADS OUTSTANDING 114,655 Abeyance warrants 14,000 $50 warrants (Expire 16 Dec 2025) 280,000 $6.5 warran

  42. Slide 42: Board of Directors

    CLICK TO EDIT MASTER TITLE STYLE 42 Mark Germain, Chairman Aentib Group (Managing Director). Founder, director, chairman, and/or investor in over 20 biotech companies including Alexion, Incyte, Neurocrine, Ariad, ChromaDex. Amir Reichman, CEO NeuroDerm Ltd (Senior Scientist), Novartis Vaccines USA (

  43. Slide 43: Significant Potential for Value Creation

    CLICK TO EDIT MASTER TITLE STYLE 43 SIGNIFICANT POTENTIAL FOR VALUE CREATION  Pipeline of NanoAb - based drugs  Promising preclinical results  Preparing for first - in - human clinical trial of anti - IL - 17 NanoAb  Collaboration with Max Planck Society and UMG, Germany  Targeting diseases wit

  44. Slide 44: Contact

    CLICK TO EDIT MASTER TITLE STYLE NASDAQ: SCNI www.scinai.com June 2024 Contact: Amir Reichman, CEO ir@scinai.com +972 - 8 - 930 - 2529

Scinai Immunotherapeutics — Investor Presentation (June 2024) on 6ix