Legend Biotech Corp. · NASDAQ:LEGN

Legend Biotech — Investor Presentation (January 2025)

29 slides from Legend Biotech's investor presentation, Jan 14, 2025

  1. Slide 1: Legend Biotech Corporate Presentation

    1 Legend Biotech CORPORATE PRESENTATION JANUARY 14, 2025

  2. Slide 2: Disclaimer

    2 Disclaimer This presentation has been prepared by Legend Biotech Corporation (“Legend Biotech” or the “Company”) solely for information purpose and does not contain all relevant information relating to the Company. The safety and efficacy of the agents and/or uses under investigation discussed in

  3. Slide 3: Legend Biotech – Transforming Cancer Care

    3 1. As of September 30, 2024 11 Pipeline Programs in Hematologic Malignancies, Solid Tumors, and Autoimmune Diseases Legend Biotech – Transforming Cancer Care Pioneer and Leader in CAR - T Therapy Revolution 2,500+ Employees 450+ Focused on R&D Stand - alone with End - to - end Capabilities Partner

  4. Slide 4: CARVYKTI Proven Leader on the Path to Cure

    4 CARVYKTI ® Proven Leader on the Path to Cure First and only CAR - T cell therapy providing superior OS vs SoC in Multiple Myeloma >4,500 treated patients treated Significant sales growth trajectory, strong 2L+ launch with the OS benefit achieved Strongest CAR - T launch to date, with $286M in net

  5. Slide 5: Multiple Myeloma Blood Cancer with a High Unmet Need

    CI, confidence interval; PI, Proteasome Inhibitor; IMiD, immunomodulatory drug; MM, multiple myeloma; OS, overall survival 1. Globocan 2022 World Fact Sheet: https://gco.iarc.who.int/media/globocan/factsheets/cancers/35 - multiple - myeloma - fact - sheet.pdf. Accessed March 2024. 2. Globocan 2022 W

  6. Slide 6: Legend and J&J Global Collaboration

    6 Legend and J&J Global Collaboration Worldwide Collaboration and License Agreement to Develop and Commercialize Cilta - cel with J&J, the #1 Global Multiple Myeloma Market Leader 50/50 United States Europe 50/50 Japan 50/50 Working Together to Realize CARVYKTI’S $5B+ Potential

  7. Slide 7: CARVYKTI - First in MM to Achieve OS Benefit vs SOC

    7 CARVYKTI ® - First CAR - T in MM to Achieve OS Benefit vs SOC Gold Standard for Oncology Trials • One - time infusion significantly prolonged overall survival and improved quality of life 1 • 45% reduction in risk of death with CARVYKTI ® vs SOC in patients w i th lenalidomide - refractory MM afte

  8. Slide 8: Maximizing Our CARVYKTI Market Leadership

    8 MAXIMIZING OUR CARVYKTI MARKET LEADERSHIP

  9. Slide 9: A New Standard for Launches

    9 Data Source: Companies' public filings. A New Standard for CAR - T Launches CARVYKTI ® - I NDUSTRY LEADI NG EARLY LAUNCH PERFO RMANCE FI RST TEN Q UARTERS O UTPERFO RMI NG HI STO RI CAL CAR - T LAUNCHES Quarterly sales ($MM) 286 102 387 98 224 124 450 400 350 300 250 200 150 100 50 0 Q1 Q2 Q3 Q4 Q

  10. Slide 10: CARVYKTI Uptake Continues

    10 CARVYKTI ® Uptake Continues Continued Market Penetration and Earlier Lines of Treatment Represents Significant Opportunity for Continued Growth QoQ Growth 2 YoY Growth 1 54% 84% U.S. 35% 125% OUS 53% 88% Global 24 55 55 70 114 140 146 140 167 258 0 0 0 2 3 12 13 16 20 27 0 50 100 150 200 250 CARV

  11. Slide 11: Earlier Line Studies Another Opportunity to Change the Treatment Paradigm

    ASCT, autologous stem cell transplant; DVRd, daratumumab, bortezomib, lenalidomide, dexamethasone; NDMM, newly diagnosed multiple myeloma; VRd, bortezomib, lenalidomide, dexamethasone. 1. Clinicaltrials.gov: NCT04133636. 2. Clinicaltrials.gov: NCT04923893. 3. Clinicaltrials.gov: NCT05257083. CARTITU

  12. Slide 12: Unlocking the Blockbuster Global Market Opportunity

    12 Unlocking the Blockbuster Global Market Opportunity MULTIPLE MYELOMA PATIENTS ELIGIBLE FOR CAR - T THERAPY Frontline : ~52k patients 2L to 4L: ~80k patients 5L+ : ~22k patients 1. MHLW is the Ministry of Health, Labour and Welfare in Japan. 2. NMPA is the National Medical Products Administration

  13. Slide 13: Outpatient Administration: Key Competitive Advantage

    13 Outpatient Administration: Key Competitive Advantage • Extensive use of CARVYKTI in outpatient setting is a key differentiator - Unique delayed CRS 1 onset allows for outpatient administration options to best serve patient needs • Patients and caregivers prefer to return home after treatment • Su

  14. Slide 14: Global Manufacturing Footprint

    14 Global Manufacturing Footprint Raritan, NJ US / EU / JP / ROW Launch/ Commercial Site for CARVYKTI ® x GMP Operational • Approval of new Raritan section expected in 2H25 Morris Plains, NJ Novartis CMO Site x Clinical production started July 2024 • Commercial production expected in 1H 2025 Expandi

  15. Slide 15: US and EU CARVYKTI Supply Overview

    15 US and EU CARVYKTI ® Supply Overview 1H22 2H22 1H23 2H23 1H24 2H24 1H25 2H25 1H26 2H26 1H27 2H27 2028 2029 2030 Launch Facilities Expansion/ Process Optimization Raritan Slot Ramp Up Obelisc Clinical + Commercial Online Tech Lane Online CMO Online Raritan Physical Expansion Facilities Driving To

  16. Slide 16: Building Upon CARVYKTI's Leadership Position

    16 1. ATC – Authorized treatment center Building Upon ‘s Leadership Position 2022 2023 Indication Expansion Deepening Community Penetration Preparing for 1L Use Data Generation in Support of CARVYKTI ® Redefining Treatment Expectations in MM 4L+ Approval 2L+ Approval Continued Market Leadership 2026

  17. Slide 17: Building Next Generation Programs

    17 BUILDING NEXT GENERATION CAR - T PROGRAMS

  18. Slide 18: Pipeline

    18 *I n collaboration with Janssen, Pharmaceutical Companies of Johnson & Johnson. † Phase 1 investigator - initiated trial in China. ‡ IND applications have been cleared by the U.S. FDA. # Subject to an exclusive license agreement with Novartis Pharma AG. The safety and efficacy of the agents and/o

  19. Slide 19: Our Differentiated R&D Approach

    19 Our Differentiated R&D Approach Potential best - in - class proprietary technology platforms and end - to - end capability Armoring strategy for solid tumors Multiple armored CAR - T strategies to overcome challenges in treatment of solid tumors Diverse platform for allogeneic treatments Diverse

  20. Slide 20: Legend and Novartis Collaboration

    20 Legend and Novartis Collaboration Legend and Novartis have an exclusive, global license agreement to advance certain DLL3 - targeted CAR - T therapies, including LB2102, an investigational therapy for small cell lung cancer.

  21. Slide 21: Small Cell Lung Cancer A Large Unmet Medical Need

    21 Small Cell Lung Cancer A Large Unmet Medical Need US: Incidence is ~35,000 1 Lung Cancer is the Second Most Diagnosed Cancer in the US 1 And the leading cause of cancer death in both men and women, accounting for ~ 20 % of all cancer deaths 1 and in 2 out of 3 people with SCLC have extensive stag

  22. Slide 22: LB2102: Legend Armored Targeting DLL3 For Small Cell Lung Cancer

    22 LB2102: Legend Armored CAR - T Targeting DLL - 3 For Small Cell Lung Cancer TARGET • DLL - 3, a promising target with prevalent & homogeneous expression in SCLC (~80% positive) and other neuroendocrine tumors • Minimal to no expression in normal tissues MoA/Scientific Rationale • Tandem humanized

  23. Slide 23: LB1908: Legend Targeting CLDN18.2

    23 LB1908 (LCAR - C18S): Legend CAR - T Targeting CLDN18.2 For gastric cancer, esophageal cancer and pancreatic cancer TARGET • Claudins (CLDN) are a family of tight junction proteins 1 - CLDN18.2 is expressed in gastric cancer and pancreatic cancer 2 MoA/Scientific Rationale • LB1908 targets CLDN 1

  24. Slide 24: Upcoming Anticipated Legend Milestones

    24 * Novartis Pharmaceuticals Corporation Upcoming Anticipated Legend Milestones COMMERCIAL • Increasing demand and deepening penetration into the community • Outpatient program expansion • OS label update CLINICAL • Topline data in CART - 5 • Advance pipeline programs, advance two programs into IND

  25. Slide 25: Legend Biotech is the proven leader forging the path to cure

    25 is the proven leader forging the path to cure.

  26. Slide 26: Thank You

    BIOTECH THANK YOU

  27. Slide 27: Appendix

    eIOTECH APPENDIX

  28. Slide 28: Parkinsonism Incidence Decreased to <1% in CARTITUDE-4

    28 Parkinsonism Incidence Decreased to <1% in CARTITUDE - 4 CARTITUDE - 1 • 5 cases of Parkinsonism (5%) with median 12.4 months of follow up (ASH 2020) • In the label, CARTITUDE - 1: 6% (4% Grade 3/4) (n=97) CARTITUDE - 4 • 1 case of Parkinsonism ( 0.6% , Grade 1) with median 15.9 months follow up

  29. Slide 29: Competitive Landscape in RRMM Treatment

    Competitive Landscape in RRMM Treatment Trial Comparator PFS (months) PFS HR OS (months) OS HR 0.55 NR vs NR 0.29 NR vs 11.8 PVd or DPd CARTITUDE - 4 Carvykti 1.01 41.1 vs 37.9 0.49 13.8 vs 4.8 SoC KarMMa - 3 1 Abecma 0.94 35.6 vs 31.6 0.56 11.7 vs 6.9 Vd OPTIMISMM 2 PVd 0.82 34.4 vs 23.7 0.66 9.9 v

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