Astellas Pharma Inc. · TSE:4503

Astellas Pharma — Corporate Update (March 2024)

25 slides from Astellas Pharma's corporate update, Mar 29, 2024

  1. Slide 1: VYLOY (Zolbetuximab) Japan Regulatory Update

    VYLOY™ (ZOLBETUXIMAB) JAPAN REGULATORY UPDATE March 29, 2024 (JST)

  2. Slide 2: Cautionary Statement Regarding Forward-Looking Information

    CAUTIONARY STATEMENT REGARDING 2 FORWARD-LOOKING INFORMATION In this material, statements made with respect to current plans, estimates, strategies and beliefs and other statements that are not historical facts are forward-looking statements about the future performance of Astellas. These statements

  3. Slide 3: Agenda

    AGENDA 3 Presenter I Gastric Cancer Disease State VYLOY Product Profile & II Commercial Strategy John Demaree Head, Strategic Brand Marketing, Oncology III Future Plans Q&A Participants IV Q&A Tomoko Nakajima, Ph.D. Shelley Shaw Asset Lead, zolbetuximab Global Brand Lead, zolbetuximab PROPRIETARY IN

  4. Slide 4: Gastric Cancer Disease State

    GASTRIC CANCER DISEASE STATE PROPRIETARY INFORMATION—FOR USE WITH INVESTORS ONLY. NOT FOR PROMOTIONAL USE.

  5. Slide 5: Gastric Cancer Has a Devastating Impact on Patients

    GASTRIC CANCER HAS A DEVASTATING IMPACT ON PATIENTS 5 ~1 Million Cases of Gastric Cancer Diagnosed Globally in 20221 3rd Deadliest Cancer in Japan1 US 26,000 Europe >70% 136,000 China Japan Early Detection of 359,000 127,000 Gastric Cancer in Japan2 Effective Treatment Options Are Limited PROPRIETAR

  6. Slide 6: Patients with CLDN18.2 Positive Gastric Cancer Need New Treatment Options

    PATIENTS WITH CLDN18.2 POSITIVE, UNRESECTABLE, ADVANCED OR 6 RECURRENT GASTRIC CANCER NEED NEW TREATMENT OPTIONS 78% 78% of 1L advanced gastric cancer population is HER2-negative 3 In Japan, chemotherapy ± CPI is the current standard of care4 Oncologists are seeking new treatment options that may im

  7. Slide 7: CLDN18.2 Is a Novel Biomarker in Advanced Gastric Cancer

    CLDN18.2 IS A NOVEL BIOMARKER IN ADVANCED GASTRIC CANCER 7 High prevalence and 38% 69% strength of clinical data patients had tumors that were aided awareness of CLDN18.2 provide strong reason to CLDN18.2 positive in SPOTLIGHT and among treating HCPs in Japan**4 test for CLDN18.2 positivity GLOW tri

  8. Slide 8: Diagnostic Testing Education Resources to Support Pathologists

    DIAGNOSTIC TESTING EDUCATION RESOURCES 8 TO SUPPORT PATHOLOGISTS Claudin182.JP Unique peer-to-peer education platform on biomarker testing for pathologists PROPRIETARY INFORMATION—FOR USE WITH INVESTORS ONLY. NOT FOR PROMOTIONAL USE.

  9. Slide 9: VYLOY Product Profile & Commercial Strategy

    VYLOY PRODUCT PROFILE & COMMERCIAL STRATEGY PROPRIETARY INFORMATION—FOR USE WITH INVESTORS ONLY. NOT FOR PROMOTIONAL USE.

  10. Slide 10: The Journey of VYLOY

    THE JOURNEY OF VYLOY 10 First Approved Completion of Targeted 2 Global Treatment for Astellas Completion of Pivotal Global CLDN18.2 Acquisition of Phase 2 Phase 3 Regulatory Positive, Ganymed FAST Trial SPOTLIGHT Submissions** Unresectable, and GLOW Advanced or Trials* Recurrent Gastric Cancer *Phas

  11. Slide 11: Identifying Potential Candidates for VYLOY

    IDENTIFYING POTENTIAL CANDIDATES FOR VYLOY 11 There are approximately 400,0009 patients diagnosed globally with Stage IV mGC/GEJ** Biomarker Testing HER2 Status CLDN18.2 Status 79%*10 78%*3 38%*6,7 Tested for HER2 HER2-negative CLDN18.2 positive (and CLDN18.2 in future) *Percentages represent global

  12. Slide 12: VYLOY Provides a Targeted Treatment Option

    VYLOY PROVIDES A TARGETED TREATMENT OPTION 12 1. VYLOY is indicated for CLDN18.2 positive, unresectable, advanced or recurrent gastric cancer 2. VYLOY is first and only approved CLDN18.2-targeted therapy 3. VYLOY can be used in eligible patients regardless of combined positive score (CPS) PROPRIETAR

  13. Slide 13: Data from Pivotal Phase 3 Trials Supported Approval: SPOTLIGHT

    DATA FROM PIVOTAL PHASE 3 TRIALS SUPPORTED APPROVAL: SPOTLIGHT6 13 Median OS was the longest OS observed in a global Phase 3 trial in this patient population.11,12 *PFS was assessed per RECIST v1.1 by IRC mFOLFOX6: 5-FU, leucovorin and oxaliplatin; PFS: Progression-free survival; OS: Overall surviva

  14. Slide 14: Data from Pivotal Phase 3 Trials Supported Approval: GLOW

    DATA FROM PIVOTAL PHASE 3 TRIALS SUPPORTED APPROVAL: GLOW7 14 SPOTLIGHT and GLOW had similar overall survival hazard ratios, validating the effectiveness of zolbetuximab combined with chemotherapy.6,7 *PFS was assessed per RECIST v1.1 by IRC CAPOX: Capecitabine and oxaliplatin; PFS: Progression-free

  15. Slide 15: Safety Data from SPOTLIGHT and GLOW

    SAFETY DATA FROM SPOTLIGHT AND GLOW 15 SPOTLIGHT GLOW Incidence of serious TEAEs* was Incidence of serious TEAEs was similar between both arms similar between both arms (44.8% vs. 43.5%)6 (47.2% vs. 49.8%)7 Most frequent TEAEs in the VYLOY Most frequent TEAEs in the VYLOY versus control arms: versus

  16. Slide 16: Dr. Kohei Shitara Discusses Significance of MHLW Approval of VYLOY

    DR. KOHEI SHITARA DISCUSSES SIGNIFICANCE OF MHLW APPROVAL OF VYLOY 16 Projection Only PROPRIETARY INFORMATION—FOR USE WITH INVESTORS ONLY. NOT FOR PROMOTIONAL USE.

  17. Slide 17: Maximizing the Value of VYLOY: Leveraging Oncology Expertise

    MAXIMIZING THE VALUE OF VYLOY: LEVERAGING ONCOLOGY EXPERTISE 17 Successfully launching oncology products into areas of high unmet need Building market leadership Creating strong relationships in oncology Preparing experienced, knowledgeable, and agile sales force for readiness upon launch PROPRIETAR

  18. Slide 18: Activating Labs for Immediate Testing for CLDN18.2 Positivity in Japan

    ACTIVATING LABS FOR IMMEDIATE TESTING FOR CLDN18.2 POSITIVITY IN JAPAN 18 Recently, VENTANA® CLDN18 (43-14A) RxDx Assay, developed by 20 Labs Roche, was approved as an IHC companion diagnostic. 60 Labs At VYLOY launch, strategic partnerships with the top 3 central labs and major cancer centers will

  19. Slide 19: Future Plans

    FUTURE PLANS PROPRIETARY INFORMATION—FOR USE WITH INVESTORS ONLY. NOT FOR PROMOTIONAL USE.

  20. Slide 20: Global Launch Plan

    GLOBAL LAUNCH PLAN 20 Global Launch: ~50 VYLOY country launches Multiple launches in Asian VYLOY + Roche VENTANA CDx planned13 countries where disease incidence is highest1 Anticipated Approval Timings* FY2023 FY2024 March 26, 2024 Q2-Q3 Q2-Q4 Q4 JAPAN US EUROPE CHINA Approved Anticipated *Global re

  21. Slide 21: Looking Ahead to a Potential Pancreatic Cancer Indication

    LOOKING AHEAD TO A POTENTIAL PANCREATIC CANCER INDICATION 21 Leading cause of 5-year survival 4th cancer death in <5% globally for patients at Japan14 the metastatic stage15 Phase 2 registrational trial in metastatic pancreatic adenocarcinoma is in progress16 Potential pancreatic cancer indication r

  22. Slide 22: Key Takeaways

    KEY TAKEAWAYS 22 CLDN18.2 is a novel and highly prevalent predictive biomarker in advanced gastric cancer that can be readily detected via IHC6,7 VYLOY is approved for patients with HER2-negative, CLDN18.2 positive, unresectable, advanced or recurrent gastric cancer, which is the third deadliest in

  23. Slide 23: Thank You

    Vy ANAS NANA YS AAAS Thank You SNNANNANANA SVAN AY Ser

  24. Slide 24: Appendix

    APPENDIX PROPRIETARY INFORMATION—FOR USE WITH INVESTORS ONLY. NOT FOR PROMOTIONAL USE.

  25. Slide 25: References

    REFERENCES 25 1. Ferlay J, Ervik M, Lam F, Laversanne M, Colombet M, Mery L, Piñeros M, Znaor A, Soerjomataram I, Bray F (2024). Global Cancer Observatory: Cancer Today. Lyon, France: International Agency for Research on Cancer. Available at https://gco.iarc.fr/today. 2. Yashima K, Shabana M, Kurumi

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