Sun Pharma Advanced Research Co. Ltd. · NSE:SPARC

Sun Pharma Advanced Research — Investor Presentation (January 2021)

44 slides from Sun Pharma Advanced Research's investor presentation, January 2021

  1. Slide 1: Corporate Presentation

    Corporate Presentation January 2021

  2. Slide 2: Disclaimer

    Disclaimer This presentation and its contents are confidential and should not be distributed, published or reproduced, in whole or part, or disclosed by recipients directly or indirectly to any other person. Any failure to comply with these restrictions may constitute a violation of applicable laws.

  3. Slide 3: Company Overview

    fe sparc Company Overview

  4. Slide 4: Innovative Biopharmaceutical Company

    Innovative Biopharmaceutical Company Targeting Large Opportunities at High Capital Efficiency Successful Track Record of Targeting High Value Through a Platform Development and Opportunities with Competitive Cost Commercialization along Structure and Ecosystem with a Robust Pipeline of Innovation 2

  5. Slide 5: Built a Robust Platform in a Span of Years

    Built a Robust Platform in a Span of 15 Years SPARC Innovative USFDA approved USFDA approved XelprosTM for USFDA accepted founded Products Lipodox – a open-angle glaucoma or ocular TaclantisTM NDA for Group product hypertension and Elepsia™ XR review2 demerged developed using for partial onset seizu

  6. Slide 6: Ongoing Evolution

    Ongoing Evolution Focus on Higher Value NCEs and NBEs NDDS Best-in-Class NCEs for New Targets Validated Targets Commercializing Partnering & Investing Investing Leveraging formulation Building on chemistry Focused on new targets US$20mn+ capabilities, NDDS products expertise, focus on optimizing and

  7. Slide 7: Narrowed Focus on Innovation into Three TAs Ripe for Disruption

    Narrowed Focus on Innovation into Three TAs Ripe for Disruption Neurology Oncology Immunology Targeted therapies or Targeted therapies or Focus Area Neurodegenerative diseases molecular medicine molecular medicine No major developments in Evolving disease landscape Limited oral options Rationale pas

  8. Slide 8: Investment Highlights

    fe sparc Investment Highlights

  9. Slide 9: Key Investment Highlights

    Key Investment Highlights 01 02 Balanced risk profile Promising projects in clinical broad product portfolio development targeting high-value unmet needs in led by Vodobatinib – offering potential neurology, oncology and immunology breakthrough therapy in PD as well as improved benefit and risk prof

  10. Slide 10: Broad Product Portfolio with a Balanced Risk Profile

    Broad Product Portfolio with a Balanced Risk Profile

  11. Slide 11: Broad Product Portfolio

    Broad Product Portfolio Phase 3 NCE/ Registration Registration Marketed/ TA Asset Indication MoA Discovery Preclinical Phase 1 Phase 2 Partner NDDS Study Partnered Parkinson’s c-ABL Inhibitor NCE Disease Vodobatinib Lewy Body c-ABL Inhibitor NCE (SCC-138) Dementia Alzheimer’s Disease c-ABL Inhibitor

  12. Slide 12: Promising Projects in Clinical Development

    Promising Projects in Clinical Development Vodobatinib for Parkinson’s Disease (SCC-138)

  13. Slide 13: Vodobatinib for Parkinson's Disease (SCC-138)

    Vodobatinib for Parkinson’s Disease (SCC-138) Breakthrough Disease Modifying Drug with US$10bn Peak Sales Potential Parkinson’s Market Product Clinical Disease Opportunity Overview Summary Overview PD is caused by a No breakthrough in the c-Abl has a pivotal role in promoting Phase 1 loss of dopamin

  14. Slide 14: Vodobatinib for Parkinson's Disease: Market Opportunity

    Vodobatinib for Parkinson’s Disease (SCC-138) Market Opportunity Chronic and progressive nature of disease is a primary factor that is continuously adding to the current number of PD patients Market Size1 Key Highlights1 Commercial Potential Chronic therapy with a large United States patient populat

  15. Slide 15: Vodobatinib for Parkinson's Disease: Product Overview

    Vodobatinib for Parkinson’s Disease (SCC-138) Product Overview Vodobatinib is a highly selective and potent c-Abl inhibitor with a superior safety profile c-Abl – Critical component of neurodegeneration Vodobatinib is a highly selective and potent c- Expression ubiquitous in Pivotal role in promotin

  16. Slide 16: Summary of Pre-clinical and Clinical Results

    Vodobatinib for Parkinson’s Disease (SCC-138) Summary of Pre-clinical and Clinical results Preclinical Safety Clinical Phase 2 Study Pre-clinical Results Profile Results (“PROSEEK”) results are highly encouraging, both from the In the MPTP1 mouse model, No CV toxicity Phase 1 completed PROSEEK is th

  17. Slide 17: Vodobatinib for Parkinson's Disease: Development Plan

    Vodobatinib for Parkinson’s Disease (SCC-138) Development Plan PROSEEK may offer the first definitive proof of concept for the c-Abl hypothesis in neurodegenerative diseases, potentially creating a new class of treatment in CNS Phase 2 Study (“PROSEEK”) Overview PROSEEK: Placebo Phase 2 study in (N=

  18. Slide 18: Vodobatinib for Parkinson's Disease: Competitive Landscape

    Vodobatinib for Parkinson’s Disease (SCC-138) Competitive Landscape Vodobatinib is the most advanced c-ABL inhibitor in clinical development Drug Class MoA # of agents Competitive Positioning in clinical development Phase III c-Abl kinase Significantly lower brain concentrations achieved. c-Abl kina

  19. Slide 19: Vodobatinib for Chronic Myelogenous Leukemia (CML) (SCO-088)

    Promising Projects in Clinical Development Vodobatinib for Chronic Myelogenous Leukemia (CML) (SCO-088)

  20. Slide 20: Vodobatinib for CML: Promising Last Line Therapy

    Vodobatinib for CML (SCO-088) Promising Last Line Therapy CML Market Product Clinical Overview Opportunity Overview Summary CML is caused by a Branded 2nd and 3rd generation TKIs Targeting patients Phase 1 translocation of the abl gene retain high commercial value due who are refractory completed in

  21. Slide 21: Vodobatinib for CML: Market Opportunity

    Vodobatinib for CML (SCO-088) Market Opportunity Large patient population – steadily increasing incidence combined with a stable mortality rate Increasing Prevalence of CML1 New Cases And Deaths Per 100,000 Market Size Annual incidence of CML has increased at a (USA)2 Estimated Global growth of prev

  22. Slide 22: Vodobatinib for CML: Unmet Need to be Addressed

    Vodobatinib for CML (SCO-088) Unmet Need to be Addressed Limited treatments available for patients failing ≥ 3 lines of treatment. SCO-088 has shown promising activity in clinical trials for patients failing with ≥ 3 lines of therapy Targeting subjects failing or intolerant to ≥ 3 TKIs (including Po

  23. Slide 23: Vodobatinib for CML: Clinical Summary

    Vodobatinib for CML (SCO-088) Clinical Summary Pivotal (Part C) study ongoing and trial in the first line setting under discussion with USFDA. Clinical Pharmacology studies are ongoing in parallel with pivotal clinical study Clinical Development Plan Orphan Drug Designation approved Part A Single As

  24. Slide 24: Oral SERD for Breast Cancer (SCO-120)

    Promising Projects in Clinical Development Oral SERD for Breast Cancer (SCO-120)

  25. Slide 25: Oral SERD for Breast Cancer (SCO-120)

    Oral SERD for Breast Cancer (SCO-120) Breast Cancer Market Product Clinical Overview Opportunity Overview Summary Breast cancer is the Hormonal therapy is SoC for ~70% SCO-120 is a novel orally- active US IND filed second most common of HR+/HER2- metastatic breast SERD for the treatment of in Jan 20

  26. Slide 26: SCO-120 Development Overview & Timeline

    Oral SERD for Breast Cancer (SCO-120) Development Overview & Timeline Promising indication of efficacy – targeting human proof of concept data in next 2–3 years Pre-Clinical Summary Clinical Summary In-Vitro Proof of Concept US IND filed January, 2020 Shows robust Tumor Xenografts Expressing ERa gro

  27. Slide 27: Selective S1PR1 Modulator for Autoimmune Diseases (SCD-044)

    Promising Projects in Clinical Development Selective S1PR1 Modulator for Autoimmune Diseases (SCD-044)

  28. Slide 28: Selective S1PR1 Modulator for Autoimmune Diseases (SCD-044)

    Selective S1PR1 Modulator for Autoimmune Diseases (SCD-044) Licensed to Sun Pharma Target Market Product Clinical Indications Opportunity Overview Summary Multiple indications across Fingolimod (first-in-class S1P Developed in collaboration Multi-part Phase 1 study many therapy areas receptor agonis

  29. Slide 29: SCD-044 Mechanism of Action

    Selective S1PR1 Modulator (SCD-044) Mechanism of Action SCD-044 is a highly selective S1PR1 modulator with better cardiac safety profile than Fingolimod Mechanism of Action Fingolimod is the 1st in class S1P receptor agonist approved Being non-selective modulator, Fingolimod is associated with serio

  30. Slide 30: Efficacy and Safety Established in Phase 1 Study

    Selective S1PR1 Modulator (SCD-044) Efficacy and Safety Established in Phase 1 Study Safety profile established in Phase 1 Study Phase 1 Clinical Summary Phase 1 Clinical Data Multi-part Phase 1 study completed in Lymphocyte count reduction1 healthy volunteers D1, 2h D1, 4h D1, 8h D1, 12h D2, 24h D3

  31. Slide 31: High Quality R&D at Low Cost

    fe sparc High Quality R&D at Low Cost

  32. Slide 32: Pre-Clinical Strategy and Focus Areas

    Pre-Clinical Strategy and Focus Areas Focused on high value targets that allow SPARC to extend its scientific capabilities across TAs Focused Strategy Focus Areas for SPARC 1 Neurology Oncology Immunology Commonality in science amongst the TAs Nanotechnology Parkinson’s Disease Cancer metabolism app

  33. Slide 33: Overview of Key Pre-clinical Programs

    Overview of Key Pre-clinical Programs 10+ pre-clinical programs under development Program Summary Targets both wild type and mutant forms of the target SCO-134 Cancer resistance enzyme. First-in-class mAb Cancer resistance Opportunity in multiple tumour types. Cancer resistance Bi-specific antibody

  34. Slide 34: Strong Captive Capabilities across R&D Process Chain

    Strong Captive Capabilities across R&D Process Chain From bench to bedside Academic Collaborations with global leading academic institutions, UCSF and UMich Discovery Research Development Ideation Formulation Clinical study design Target selection development Reg. Science and execution Medicinal che

  35. Slide 35: Marquee Promoter Supported by Experienced Management Team

    Marquee Promoter Supported by Experienced Management Team

  36. Slide 36: Established and Supported by Marquee Promoter

    Established and Supported by Marquee Promoter Marquee Promoter Shareholding Public 31.54% Promoter group entities 57.74% Dilip Shanghvi 10.72% Dilip Shanghvi Providing Continuous Support and Investments Chairman and Managing Director Rights issue 2 INR250cr/US$38.2mn Founded Sun Pharmaceutical Indus

  37. Slide 37: Highly Experienced Management with Global Experience

    Highly Experienced Management with Global Experience 25 26 24 6 13 6 Anil Raghavan Nitin Dharmadhikari Siu-Long Yao CEO Executive VP of Delivery Sr. VP Clinical Development & Systems & Manufacturing Operations Responsible for strategic prioritization and portfolio Responsible for Formulations, Overs

  38. Slide 38: Highly Experienced Management with Global Experience

    Highly Experienced Management Supported with Globalby Experience Marquee Promoter 30 21 22 3 1 13 Chetan Rajpara Michael Choi Shravanti Bhowmik Chief Financial Officer VP Business Development VP of Program Management Responsible for finance, Responsible for global business Oversees all aspects of th

  39. Slide 39: Scientific Advisory Board Consisting of Highly Recognized Experts

    Scientific Advisory Board Consisting of Highly Recognized Experts Phil Needleman, PhD Rakesh Jain, PhD Robert Speigel PhD1 Mark Simon, MBA2 Prof. Emeritus Massachusetts Weill Cornell Medical College Torreya Partners, Citigroup, General Hospital PTC Therapeutics Robertson Stephens, Kidder Peabody Ala

  40. Slide 40: Financial Overview

    fe sparc Financial Overview

  41. Slide 41: Summary Financials

    Summary Financials Income Expenditure US$mn US$mn 56.3 29.0 51.1 48.9 28.1 27.5 46.8 25.1 35.8 31.1 12.9 12.2 FY16 FY17 FY18 FY19 FY20 H1 FY21 FY16 FY17 FY18 FY19 FY20 H1 FY21 Total Assets Cash Balance US$mn US$mn 30.4 57.3 47.5 41.4 36.6 34.0 16.7 24.0 12.1 1.9 1.2 3.5 FY16 FY17 FY18 FY19 FY20 H1 F

  42. Slide 42: Key Takeaways

    3 sparc Key Takeaways

  43. Slide 43: Key Takeaways

    Key Takeaways SPARC has multiple levers in place to create significant value for shareholders 1 Broad and diverse pipeline 1 across multiple modalities and Novel drug delivery, optimized MoAs and NCEs & NBEs targeting novel biologies therapeutic areas 22 Multiple upcoming key catalysts Pivotal study

  44. Slide 44: Thank You

    Thank You The SPARC Logo is a trademark of Sun Pharma Advanced Research Company Ltd . In addition to Company data, data from market research agencies, Stock Exchanges and industry publications has been used for this presentation. This material is for use during an oral presentation; it is not a comp

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