Beyondspring, Inc. · NASDAQ:BYSI

Beyondspring — Investor Presentation (April 2022)

45 slides from Beyondspring's investor presentation, April 2022

  1. Slide 1: Corporate Presentation

    Corporate Presentation APRIL 2022| NASDAQ: BYSI 1

  2. Slide 2: Disclaimer

    Disclaimer This presentation has been prepared for informational purposes only. No money or other consideration is being solicited, and if sent in response, will not be accepted. This presentation shall not constitute an offer to sell, or the solicitation of an offer to buy, any securities, nor shal

  3. Slide 3: BeyondSpring Investment Highlights

    BeyondSpring Investment Highlights (Nasdaq: BYSI) Headquarters New York, NY Committed to raising the standard of care Lead Asset Plinabulin, first-in-class, Selective Immunomodulating for cancer patients with first-in-class Microtubule-Binding Agent (SIMBA) treatments that improve lives and clinical

  4. Slide 4: Robust Plinabulin Pipeline: Near-Term NDAs & I/O Clinical Trials

    Robust Plinabulin Pipeline: 2 Near-Term NDAs & I/O Clinical Trials Indication / Trial Name / Commercial Program Preclinical Phase 1 Phase 2 Phase 3 Target Collaborator Rights1 NSCLC Plinabulin + docetaxel DUBLIN-3 Ph. 3 primary and secondary endpoints presented at ESMO ’21 Global (2nd/3rd line) Late

  5. Slide 5: Plinabulin Franchise

    Plinabulin Franchise Clinical Confirmation Expand Transform Promising early clinical efficacy data Positive topline phase 3 OS data (n=559) – 7 different cancers in phase 1/2 study Confirmed in 6 clinical studies (n>1200) & Accepted for NDA review CIN (BTD & Priority Review) NSCLC Multiple Cancers (

  6. Slide 6: Plinabulin: Pipeline in a Drug Potential

    Plinabulin: “Pipeline in a Drug” Potential - First-in-Class, Selective Immunomodulating Microtubule-Binding Agent (SIMBA) 6

  7. Slide 7: Novel Mechanism of Action

    Novel Mechanism of Action Plinabulin: First-in-Class, Selective Immunomodulating Microtubule-Binding Agent (SIMBA) - Plinabulin Induces Dendritic Cell Maturation (the most potent APC), a Key Step in Initiating Anti-Cancer Durable Response ❷ Plinabulin Stimulate maturation of dendritic cells to incre

  8. Slide 8: Plinabulin Clinical Program Overview

    Over 700 Patients Treated with Plinabulin to date in Clinical Program; NB SS DI CIN Prevention benefit shown in 6 trials A Q Study 101 Phase 1/2 Phase 2 Efficacy Data Phase 2 Phase 3 Registration Anti- Cancer Study 103 (DUBLIN-3, n=559) 4.6 month mOS Plinabulin + Docetaxel vs. Plinabulin + extension

  9. Slide 9: Plinabulin Opportunity

    Plinabulin Opportunity 1 Plinabulin is a novel mechanism, first-in-class immunomodulating microtubule-binding agent, complementary to existing standard of care 2 Near-term NDA and revenue opportunity in China for Chemotherapy Induced Neutropenia (CIN) Prevention, with commercial partner Hengrui 3 DU

  10. Slide 10: Delivering the Plinabulin Value Proposition

    Delivering the Plinabulin Value Proposition Near Term Opportunity Longer-Term Potential CIN Prevention ANTI-CANCER Raise the Standard of Care w/ Immuno-Oncology Potential NSCLC APC Cornerstone of Improve Survival and emerging regimens Quality of Life 10

  11. Slide 11: Chemotherapy-induced Neutropenia (CIN) Prevention Indication

    Chemotherapy-induced Neutropenia (CIN) Prevention Indication 11

  12. Slide 12: Unmet Medical Need in Week 1 After Chemotherapy

    CIN Unmet Medical Need in Week 1 After Chemotherapy Despite widespread G-CSF use, CIN is #1 reason for FN, ER visits, hospitalization, sepsis, mortality, and chemotherapy dose reduction and disruption 1 Short-term Long-term G-CSF is more effective in week 2 after Chemotherapy’s anti-cancer chemo in

  13. Slide 13: Chemotherapy Without Compromise: Turning the Ds into the 4 Ss

    CIN Chemotherapy Without Compromise: Turning the 4 Ds into the 4 Ss DECREASED STABLE DOSE recommended dose maintaining >85% Plinabulin + G-CSF DELAYED cycles SUSTAINED CYCLES cycles on time • Differentiated clinical profile, potential to improve SOC DISCONTINUED chemotherapy STAY THE COURSE complete

  14. Slide 14: Plinabulin + G-CSF Combination Addresses Unmet Medical Need

    CIN Plinabulin + G-CSF Combination Addresses Unmet Medical Need Plinabulin is the only product in development that has demonstrated the potential to elevate the standard of care (SOC) to prevent CIN 7.0 Pegfilgrastim 6 mg (n=22) • Breakthrough Therapy Designation: Unmet Plinabulin 20 mg/m2 + Pegfilg

  15. Slide 15: Protective-2 Ph 3: Registration Study Design

    CIN Protective-2 (Study 106) Ph 3: Registration Study Design • Double blind, global study (19 centers); 4 cycles • Covance: CRO • Covance Central Lab: ANC evaluation Plinabulin 40mg + Pegfilgrastim 6 mg N=111 Breast Cancer, R 1:1 TAC Therapy Placebo + Pegfilgrastim 6 mg N=110 15

  16. Slide 16: PROTECTIVE-2 Phase 3: Primary Endpoint Met

    CIN PROTECTIVE-2 Phase 3: Primary Endpoint Met Proportion of Patients with NO Grade 4 Neutropenia (or DSN= 0 Days) in Cycle 1 35.0% Global 31.5% China 30.0% (p=0.0015) (p=0.0015) 24.1% 25.0% DSN=0 20.0% 13.6% N=111 15.0% 全球 N=110 N=58 10.0% N=110 3.5% 5.0% N=57 0.0% Pegfilgrastim Plinabulin 40 mg +

  17. Slide 17: Favorable Benefit/Risk Ratio

    CIN Favorable Benefit/Risk Ratio (Plinabulin + G-CSF vs. G-CSF alone) Improved Efficacy (ANC based Improved Efficacy (FN) Favorable Safety in Cycle 1) – 106 Phase 3 – 106 Phase 3 – 106 Phase 2+3 No Grade 4 Neutropenia FN Grade 4 TEAE (primary endpoint) • 3.6% vs. 6.3% (incidence) • 20% less Grade 4

  18. Slide 18: China NMPA Review Ongoing; Discuss Regulatory Pathway with U.S. FDA

    CIN China NMPA Review Ongoing; Discuss Regulatory Pathway with U.S. FDA Seeking Approval for “Plinabulin + G-CSF Combination” in CIN Prevention Registration Study Supporting Studies Supporting Studies Plinabulin + G-CSF combo Plinabulin vs. placebo vs. G-CSF mono Plinabulin vs. G-CSF (Dublin-3, phas

  19. Slide 19: Plinabulin Has Potential Use Across the Spectrum of Solid Tumors

    CIN Plinabulin Has Potential Use Across the Spectrum of Solid Tumors G-CSF Administrations: Solid Tumor Rectal Cancer Gynecological 5% Cancer, Other G-CSF Use by Cancer type: Ovarian 5% Cancer • Improved control of CIN with 5% Plinabulin can prove important in Prostate Cancer cancers with more aggre

  20. Slide 20: Potential to Elevate Standard of Care for CIN Prevention

    CIN Potential to Elevate Standard of Care for CIN Prevention Opportunity Unmet need Product differentiation ✓Market size ✓Grade 4 neutropenia complications Plinabulin + G-CSF addresses 3 oncologist ✓Market growth ✓CIN: #1 reason for therapy change needs: ✓NCCN guideline change (4Ds) ✓ Keeps ANC out

  21. Slide 21: 2nd/3rd line NSCLC Indication

    2nd/3rd line NSCLC Indication 21

  22. Slide 22: Severe Unmet Medical Needs – 2nd/3rd Line NSCLC, EGFR Wild Type

    Anti-Cancer Severe Unmet Medical Needs – 2nd/3rd Line NSCLC, EGFR Wild Type • Large patient population with limited treatment Efficacy options o EGFR wild type: ~85% western NSCLC and ~70% of Asian NSCLC patients Safety o With immunotherapies moved to first line, Docetaxel-based therapies are the ma

  23. Slide 23: Underserved Market: 2nd/3rd Line NSCLC Treatment

    Anti-Cancer Underserved Market: 2nd/3rd Line NSCLC Treatment With PD-1/PD-L1 Moved To First Line, Patients are Left with Efficacy and Safety Tradeoffs and Suboptimal Regimens Treatment Ramuciramab + Docetaxel vs. Docetaxel1 Pemetrexed vs Docetaxel2 Low CIN risk Pros Limited efficacy; OS HR: 0.86 (se

  24. Slide 24: DUBLIN-3: Docetaxel + Plinabulin vs. Docetaxel + Placebo

    Anti-Cancer DUBLIN-3: Docetaxel + Plinabulin (DP) vs. Docetaxel + Placebo (D) in Patients With 2nd/3rd line NSCLC, EGFR wild type Global, Randomized, Single-Blinded (blinding for patients only) Stratified for: Region (Asia/non-Asia), Prior Line, ECOG score Around 60 sites: U.S., China, and Australia

  25. Slide 25: Met Primary Objective in Overall Survival (OS)

    Anti-Cancer Met Primary Objective in Overall Survival (OS) HR = 0.82 25

  26. Slide 26: Significantly Increase Long-term OS Rate

    Anti-Cancer Significantly Increase Long-term OS Rate 26

  27. Slide 27: Significant Improvement in PFS, Double ORR

    Anti-Cancer Significant Improvement in PFS, Double ORR HR = 0.76 Log rank P = 0.0082 27

  28. Slide 28: Significant Reduction in Grade 4 Neutropenia

    Anti-Cancer Significant Reduction in Grade 4 Neutropenia Cycle 1 Day 8 and All Cycles Day 8 Grade 4 neutropenia, Cycle 1 Day 8 Grade 4 neutropenia, All Cycles Day 8 100% 100% 90% 90% P<0.0001 P<0.0001 Percentage of Patients Percentage of Patients 80% 80% 70% 70% 60% 60% 50% 50% 40% 40% 33.58% 30% 27

  29. Slide 29: Significant Improve Quality of Life Benefit - Q-TWiST

    Anti-Cancer Significant Improve Quality of Life Benefit - Q-TWiST (Quality-Adjusted Time Without Symptoms of Disease and Toxicity) Plinabulin + Docetaxel Docetaxel alone Clinically Meaningful Improvement of >18% in Q-TWiST. 29

  30. Slide 30: Dublin-3: Superior Efficacy and Significant Reduction in Grade 4 CIN

    Anti-Cancer Dublin-3: Superior Efficacy and Significant Reduction in Grade 4 CIN (DP vs. D) Plinabulin (30 mg/m2) Docetaxel (75 mg/m2) Primary Endpoint + Docetaxel (75 mg/m2) N=281 N=278 OS (months or M) Mean 12.77 M (0.676) Mean 15.08 M (0.848); p=0.03 Median 10.5 M (9.3, 11.9), Log-rank p=0.0399 M

  31. Slide 31: IO Combinations

    BeyondSpring 10 Combinations

  32. Slide 32: Plinabulin as Potential Cornerstone Add-on Therapy to Current I/O Regimens

    Plinabulin as Potential Cornerstone Add-on Therapy to Current I/O I/O Regimens to Address Severe Unmet Medical Needs PD-1/PD-L1 Inhibitors Potential to greatly expand - $30B global annual sales the addressable market Current Severe Unmet Medical Needs Plinabulin Clinical Development • PD-1/PD-L1 res

  33. Slide 33: Plinabulin in Triple Combo Development for Multiple Cancer Indications

    Plinabulin in Triple Combo Development for Multiple Cancer Indications I/O in PD-1/PD-L1 Failed Patients Trial Name / Status Indication / Target Program Commercial Rights Collaborator SCLC Plinabulin + 7 US sites, including Phase 1 completed, Checkpoint naïve and Nivolumab (PD-1) + Rutgers Universit

  34. Slide 34: Efficacy Analysis (Phase I) Plinabulin + Nivolumab + Ipilimumab in SCLC

    I/O Efficacy Analysis (Phase I) Plinabulin + Nivolumab + Ipilimumab in SCLC PD-1/PD-L1 PD-1/PD-L1 resistant Efficacy Analysis therapy naïve (n=7) (n= 6) Number of 3 (50%) 3 (43%) patients with PR *PR –Partial Response - RESIST 1.1 : At least a 30% decrease in the sum of diameters of target lesions,

  35. Slide 35: Plinabulin as a Potential Synergistic Cornerstone Agent in I/O Therapy

    I/O Plinabulin as a Potential Synergistic Cornerstone Agent in I/O Therapy Data Conclusion • High response rate to previous CPI • Immune system re-sensitized failures (43%) • Improved Anti-cancer Response • Increased antigen presentation (46% ORR vs. 12-23% CPI) simulates T cell activation • Durable

  36. Slide 36: Commercial Plan in China

    * BeyondSpring Commercial Plan in China

  37. Slide 37: Commercial Potential in CIN Prevention Market in China

    Commercial Potential in CIN Prevention Market in China G-CSF product annual sales in China (¥100,000,000) Overview of marketed long-acting G-CSF products in China2 Product Company Approval Date +30% 803 Jinyouli 28 Short-lasting G-CSF CSPC 2012 (津优力) 501 Xinruibai 381 Qilu 2015 20 (新瑞白) 291 52 21 Ai

  38. Slide 38: Rapid Growth in China's NSCLC Market

    Rapid Growth in China’s NSCLC market NSCLC drug sales in China1 (¥100,000,000 or $15.7 M USD) 52 17 30 17 7 ⚫ Between 2015 and 2019, the number of new cases of NSCLC in China increased from 669,000 to 761,000, and the number of new cases is expected to reach over 1 million by 20301. ⚫ NSCLC drugs sa

  39. Slide 39: Hengrui is the Ideal Partner for Plinabulin in Greater China

    Hengrui is the Ideal Partner for Plinabulin in Greater China Exceptional synergy between plinabulin and Hengrui pipeline ➢ Hengrui is the leader in oncology product R&D and commercialization in China • Established in 1970; Listed on Shanghai Stock Exchange in 2000 (Shanghai stock exchange ticker: 60

  40. Slide 40: Hengrui Partnership Supports Key Commercialization Goals in China

    Hengrui Partnership Supports Key Commercialization Goals in China Manages commercialization risk and optimizes return on plinabulin franchise • Leverages existing infrastructure of leading oncology player • Minimizes launch investment and risk • Optimizes near-term return through performance-related

  41. Slide 41: Corporate Highlights

    BeyondSpring Corporate Highlights

  42. Slide 42: Plinabulin: Hengrui and Wanchunbulin Partnership in Greater China

    Plinabulin: Hengrui and Wanchunbulin Partnership in Greater China (BeyondSpring Inc. owns 58% of Wanchunbulin) Hengrui is the oncology leader in China, with great synergies with Plinabulin - Manages commercialization risk and optimizes return on plinabulin franchise Hengrui: Plinabulin Rights in Gre

  43. Slide 43: SEED Therapeutics Subsidiary – Pipeline Potential

    SEED Therapeutics Subsidiary – Pipeline Potential SEED: Subsidiary pursuing "Molecular Glue" targeted protein degradation to degrade disease-causing proteins previously believed to be undruggable • $800M collaboration with Eli Lilly on three targets • Own targets (e.g., KRAS) • Structure conducive t

  44. Slide 44: BeyondSpring: Key Highlights

    BeyondSpring: Key Highlights Committed to raising the standard of care for cancer with first-in-class treatments that improve lives and Mission clinical outcomes for millions of patients in need Near-term Global Capabilities Broad Pipeline Global Market Opportunities Continuous Innovation Plinabulin

  45. Slide 45: www.beyondspringpharma.com

    www.beyondspringpharma.com 45

BeyondSpring — Investor Presentation (April 2022) on 6ix