Jubilant Pharmova Limited · NSE:JUBLPHARMA

Jubilant Pharmova — Investor Presentation (April 2025)

77 slides from Jubilant Pharmova's investor presentation, Apr 9, 2025

  1. Slide 1: Investor Presentation Apr'25

    Investor Presentation Apr’25

  2. Slide 2: Forward-looking statements disclaimer

    Statements in this document relating to future status, events, or circumstances, including but not limited to statements about plans and objectives, the progress and results of research and development, potential product characteristics and uses, product sales potential and target dates for product

  3. Slide 3: Strong presence in diverse sectors

    Strong presence in diverse sectors • Pharmaceuticals • Contract Research & Development Services • Life Science Ingredients • Therapeutics • Performance Polymers • Auto Dealerships • Food Service (QSR) • Oil and Gas services Global presence through investments • India • Europe • Africa • USA • Singap

  4. Slide 4: Radiopharma, Allergy Immunotherapy, CDMO, CRDMO, Generics, Novel Drugs

    Radiopharma Allergy Immunotherapy CDMO Sterile Injectables Leading manufacturer 2nd largest player Leading contract manufacturer of Radiopharmaceuticals in the US Allergenic extract market in North America in North America Sole supplier of Venom Serves top global innovator pharma 2nd largest radioph

  5. Slide 5: Business wise and geography wise revenue split

    Business wise Revenue Split Geography wise Revenue Split FY24 FY24 India, 3% Generics, Rest of 12% World, Europe, 7% 9% Allergy Immunotherapy, 10% Radiopharma, 45% CRDMO, North 16% America, 80% CDMO - SI, 17% Specialty Products (Radiopharma, Allergy Immunotherapy) and Specialty Services (CDMO & CRDM

  6. Slide 6: Manufacturing and research facilities

    Kirkland, Montreal, Canada Spokane, Washington, US CDMO – SteriIe Injectables Radiopharmaceuticals CDMO – SteriIe Injectables Allergy Immunotherapy NORTH AMERICA 6 Manufacturing facilities Roorkee, Uttrakhand, India - Generics Nanjangud, Karnataka, India - CDMO API 2 Research facilities INDIA 46 Rad

  7. Slide 7: 2x Revenue, 25% EBITDA Margin, Zero Net Debt

    From To FY24 FY30* 2x Revenue Rs. 6,703 Cr. Rs. 13,500 Cr. 25% EBITDA Margin ~ 15 % 23% to 25% Zero Net Debt Rs. 2,457 Cr. Zero High Teens RoCE High Single digit High Teens * Future numbers projected on constant currency basis 7

  8. Slide 8: Business Growth Drivers

    Business Growth Drivers Leadership in Ruby-Fill® Radiopharma Launch New PET, SPECT and Therapeutic products (MIBG) Invest in 6 high margin PET Radiopharmacies in US Allergy immunotherapy Strengthen competitive position and develop new products CDMO - Sterile Injectables Double capacity in Spokane, U

  9. Slide 9: Radiopharma

    Radiopharma

  10. Slide 10: Radiopharmaceuticals growing role in treatment of diseases

    SPECT PET Radiopharmaceutical Imaging Imaging Therapeutics Low Energy High Energy Systemically or Locally gamma rays positrons Delivered detected by SPECT cameras detected by a PET scanner radiation using pharmaceuticals Isotopes - Tc99m Isotopes - Rb82, F18, Ga68 Isotopes – I131, Lu177, Ac225 MAA,

  11. Slide 11: Growth Drivers & Trends

    US Radiopharmaceutical Market Growth Drivers & Trends USD Bn. ~ 20 Launch of advanced • PSMA Therapeutic, Pluvicto for Prostrate Cancer ~USD 2.0 Bn. Therapies CAGR: New • PSMA Diagnostics for Prostrate Cancer ~ USD 1.5 Bn. 20%+ • Broad range of applicability e.g. Alzheimer’s products in • Special re

  12. Slide 12: Stringent regulation, time sensitive logistics, forward integration

    Stringent manufacturing & regulatory environment Adherence with extensive license framework. Stringent manufacturing set up required to handle isotopes Managing time sensitive Forward integration logistics with radiopharmacies Radioactive isotope decays Forward integration with exponentially. The ha

  13. Slide 13: PET Dx, SPECT Dx and therapeutics products

    Organ Key Indication Product PET Dx Cardiac Coronary Artery disease Ruby - Fill® Breast Lymph nodes detection Sulfur Colloid Cardiac blood pool imaging Tc99m-Gluceptate Cardiac • Diversified across diagnostics & therapeutics Coronary Artery Disease Tc99m-Sestamibi • Current TAM at USD 400 Mn. Gastro

  14. Slide 14: Draximage MAA, DTPA, Ruby-Fill, HICON

    Draximage ® MAA Draximage ® DTPA Ruby-Fill ® HICON® Sodium Iodine I 131 Solution USP It is used for Cardiac PET scan, MAA is used in the perfusion DTPA is used to assess HICON® is a radioactive to evaluate regional myocardial phase of a ventilation/perfusion pulmonary ventilation function in therape

  15. Slide 15: Radiopharmaceuticals quarterly results

    Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y • Q3’FY25 revenue grew 10% YoY on back of growth in Ruby-Fill ® and new product, Sulphur Colloid Revenue 241 251 265 10% 696 778 12% • Q3’FY25 EBITDA flattish YoY due to change in EBITDA 126 120 125 (1%) 352 370 5% product mi

  16. Slide 16: Radiopharmaceuticals FY30 targets

    Revenue: More than 2x of FY24 EBITDA Margin: More than 50% Growth drivers: • Ruby-Fill® Revenue: Rs. 952 Cr. • New PET & EBITDA Margin: 50% Revenue: Rs. 872 Cr. SPECT products EBITDA Margin: 53% • MIBG FY23 FY24 FY30 16

  17. Slide 17: Ruby-Fill Rubidium generator and Elusion System

    Ruby-Fill ® Rubidium 82 generator and Elusion System Growth drivers: Competitive advantage • Ruby-Fill® • Longer life per generator (7 weeks vs 6 weeks for peer) • New PET & SPECT • Better image quality and consistency products • Saline Push feature • MIBG Current Position • Market Size ~ USD 160 Mn

  18. Slide 18: New products in SPECT and PET imaging

    Developing new products in SPECT Imaging to maintain leadership & in PET Imaging for growth Growth drivers: • Ruby-Fill® Incremental TAM Potential Peak Annual Timeline No. of launches • New PET & SPECT USD Mn. Sales - USD Mn. products FY27 50 20 2 • MIBG FY28 250 60 3 FY29 250 40 4 Total 550 120 9 1

  19. Slide 19: HICON and MIBG

    HICON® Sodium Iodide I 131 - Commercialised MIBG - Undergoing Clinical trials Growth drivers: • Ruby-Fill® • Potential peak sales • New PET & SPECT USD 70 - 100 Mn. products • Data package to FDA • MIBG by H2’FY26 • Iodine I 131, HICON® is standard care for patients • Used in imaging & treatment for

  20. Slide 20: Radiopharmacy

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  21. Slide 21: Growth Drivers & Trends

    Growth Drivers & Trends SPECT Radiopharmacy PET Radiopharmacy • Consolidated market in the US. Large M&A transactions in Radiopharmacies • Increasing demand for novel PET products driving PET radiopharmacies growth • Stringent USP 825 regulations to drive increase in therapeutics dispensing through

  22. Slide 22: Consolidated market and barriers to entry

    Consolidated Market Barriers to Entry 1 Stringent Regulations # of radio SPECT PET # of hospitals Each treatment site is required to obtain a license pharmacies in the US pharmacies pharmacies served in the US from Nuclear Regulatory Commission and comply with additional state, local, and hospital r

  23. Slide 23: Radiopharmacy network

    nd 46 Current SPECT Current Cyclotron 6 New PET SITES Radiopharmacies USP<825> JDR network is USP 825 with ~ 20% WD compliant Portland volume market MT ND ME share OR MN VT ID Saginaw NH SD Minneapolis WI NY Business moat 1,800 Boston Detroit Wilkes WY MI Barre Phila- RI Unique combination of delphi

  24. Slide 24: Radiopharmacies quarterly results

    Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y • Q3’FY25 revenue grew 13% YoY on the back of increase in volume from new products, however revenues growth got impacted by Industry wide Revenue 511 568 576 13% 1,488 1,715 15% Technetium shortage in Q3’FY25 EBITDA 10 6 5 (4

  25. Slide 25: Radiopharmacies FY30 targets

    Revenue: 2x of FY24 EBITDA Margin: ~ 7% to 8% Revenue: Rs. 2,050 Cr. EBITDA Margin: 3% Revenue: Rs. 1,681 Cr. EBITDA Margin: (5%) FY23 FY24 FY30 25

  26. Slide 26: PET expansion

    Growth driver: • PET expansion • Strengthened network to enable long term contracts with PET radiopharmaceutical manufacturers • Fully operational by FY28. Funding through internal accruals and long-term credit • Expect Asset turnover of 1.0x and RoCE 20% + on the USD 50 Mn. investment 26

  27. Slide 27: Allergy Immunotherapy

    Allergy Immunotherapy

  28. Slide 28: Allergies, testing and treatment

    • 20% + global population have allergies e.g. Asthma and Allergenic Rhinits • Allergy Immunotherapy requires repeated shots of allergic antigens to develop immunity Allergies Testing Treatment 28

  29. Slide 29: Global Allergy Immunotherapy Market

    Global Allergy Immunotherapy Market Growth Drivers and Trends USD Bn. • Concentrated US market with 3 players 3.0 • Complex supply chain from sourcing to processing 2.2 2.7 • Grandfathered approvals, new product needs BLA 2.0 0.2 0.3 • Market increasing in Sub-Lingual delivery 2023 2028 Non-US US •

  30. Slide 30: HollisterStier venom and allergenic extracts

    nd • 100-year-old ‘HollisterStier’ brand • Onshore US FDA approved manufacturing • Sole Supplier of Venom extracts in the US • Dedicated sales force in the US • 200+ allergenic & 6 venom extracts • 2,000+ Allergists / ENTs as customers Venom Extracts Allergenic Extracts Skin Testing Devices Venom ex

  31. Slide 31: Allergy Immunotherapy quarterly results

    • Q3’FY25 revenues grew by 7% on YoY basis. Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y • Q3’FY25 EBITDA margin decreased YoY due to Revenue 161 170 171 7% 491 509 4% weakness in exports and production challenges for specific SKU’s. EBITDA 62 46 48 (23%) 198 157 (21%)

  32. Slide 32: Allergy Immunotherapy FY30 targets

    Revenue: ~1.5x of FY24 EBITDA Margin: 35% to 40% Revenue: Rs. 679 Cr. EBITDA Margin: 40% Revenue: Rs. 603 Cr. EBITDA Margin: 34% FY23 FY24 FY30 32

  33. Slide 33: Allergy Immunotherapy growth strategy

    Strengthen competitive Grow outside US Increase investment position in US business in R&D • Retain and grow Venom • Develop new products & customers & patient base • Increase outside US technologies Venom sales through strategic partnerships in • Increase US revenue in • Build treatment European mar

  34. Slide 34: CDMO - Sterile Injectables

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  35. Slide 35: Growth Drivers & Trends

    Global CDMO-SI Market Size Growth Drivers & Trends USD Bn 20 17 16 14 • Increasing number of drugs in Biologics 13 pipeline and Loss of exclusivity • Consolidation in supply due to large acquisitions - Catalent Inc. by Novo Holding 2023 2024 2025 2026 2027 Vial filling ( Units in Billions ) Year 202

  36. Slide 36: Long contracts, high switching costs, regulatory barriers

    • Majority of commercial contracts are typically long duration (typically 3 years or more with auto renewal) • Greenfield expansion is considerably difficult due to high up-front capex required with ongoing opex to support initial product commercialization • Innovator companies prefer onshore North

  37. Slide 37: Top pharma customers and fill-finish services

    • 5 of the top 20 pharma companies as customers • 25+ customers across the world with multiple products having patent protection and limited competition • 5+ years average relationship time with Top 10 Customers • 90%+ repeat customer business • 24 months of switching timelines for customers • Full

  38. Slide 38: CDMO Sterile Injectables quarterly results

    • Q3’FY25 revenue stable YoY. Montreal facility Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y restarted operations in Q3’FY25 and operated for partial quarter. Revenue 303 302 306 1% 858 932 9% • Q3’FY25 EBITDA margins increased YoY EBITDA 37 89 51 38% 134 197 47% howeve

  39. Slide 39: CDMO Sterile Injectables FY30 targets

    Revenue : More than 2x of FY24 EBITDA Margin : More than 25% Revenue : Rs. 932 Cr. EBITDA Margin : 21% Revenue : Rs. 1,117 Cr. Revenue : Rs. 1,155 Cr. EBITDA Margin : 17% EBITDA Margin : 30% FY23 FY24 TTM Dec'24 FY30 39

  40. Slide 40: Doubling capacity timeline

    Growth driver: • Doubling Capacity Timeline FY’24 FY’25 FY’26 FY’27 FY’28 LINE 3 Installation Media Fill Tech Transfer Commercial Production LINE 4 Design Construction Installation Media Fill Commercial Production • Total investment at USD 285 Mn. ( RoCE > 20%) including US Govt. funding of USD 150

  41. Slide 41: CRDMO: Drug Discovery Services, CDMO API

    CRDMO: Drug Discovery Services, CDMO API

  42. Slide 42: Growth Drivers & Trends

    Drug Discovery Services Market Size USD Bn. Growth Drivers & Trends 10 8 Drug Discovery Market • Biosecure Act advantage • Rise in specialized technologies such as ADCs and oligonucleotides 2023 2028 CDMO API Market Size USD Bn. CDMO API Market 130 95 • Rising interest in custom generics • Rapid mom

  43. Slide 43: Top pharma customers in drug discovery

    • 8 of the top 20 pharma companies as customers with 5x increase in revenue share from large pharma • Indian Leader for “Integrated Drug Discovery”, with a track record of +85 programs and Big pharma strategic partnership • Strengthen European penetration, with multifold revenue increase • Fully int

  44. Slide 44: Drug discovery services, early and late CDMO, APIs

    Drug Discovery Services & Early CDMO Late CDMO & APIs Integrated Chemistry Research Contract Development & Advanced Intermediate CoE Biologics Drug Discovery Centre Innovation Centre Manufacturing Centre & ( St. Julien, France ) (IDDC, Bengaluru) (CIRC, G. Noida) (API CDMC) API Manufacturing ~ 35 Sc

  45. Slide 45: Drug Discovery Services quarterly results

    Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y • Q3’FY25 revenue increased 32% YoY due to increase in revenue from new contracts from large Pharma customers Revenue 114 151 150 32% 332 414 25% • Q3’FY25 EBITDA increased 27% YoY on the EBITDA 30 36 39 27% 78 96 24% back of

  46. Slide 46: Drug Discovery Services FY30 targets

    Revenue: ~ 3x of FY24 EBITDA Margin: More than 25% Revenue: Rs. 531 Cr. EBITDA Margin: 24% Revenue: Rs. 449 Cr. EBITDA Margin: 24% Revenue : Rs. 522 Cr. EBITDA Margin : 31% FY23 FY24 TTM Dec'24 FY30 46

  47. Slide 47: Biosecure Act

    Growth driver: • Add large pharma • Executing strategy on large pharma Biosecure Act • Footprint in EU • Act passed in Sep’24 by US House of Representatives • Introduction of ADCs, mAbs, and Biologics platforms • American pharma companies to look for alternatives besides China 47

  48. Slide 48: Capacity expansion at Greater Noida and Bengaluru

    Expansion at current sites, Greater Noida & Bengaluru Expansion at new site, Devanahalli, Bengaluru Capacity : 1,000 FTE’s ( FY25 )  2,000 FTE’s ( FY26 )  4,000 FTE’s ( FY27 ) Total Capex USD 150 Mn. ( Expect RoCE > 20% ) 48

  49. Slide 49: Expanded TAM in mAbs and ADCs

    • Expanded TAM by USD 1.4 Bn. in mAbs and ADCs • Added strategic footprint in the EU • Enhanced domain expertise in ADC • Unique & cost-effective delivery model 49

  50. Slide 50: CDMO API quarterly results

    Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y • Q3’FY25 revenue stable YoY. Industry wide pricing pressure continues Revenue 138 127 142 3% 480 399 (17%) • Q3’FY25 EBITDA margins increased YoY due to cost optimization efforts and improvement in EBITDA 11 12 20 82% 39 49

  51. Slide 51: CDMO API FY30 targets

    Revenue: 2x of FY24 EBITDA Margin: More than 15% Revenue: Rs. 663 Cr. Revenue: Rs. 645 Cr. EBITDA Margin: 5% EBITDA Margin: 10% FY23 FY24 FY30 51

  52. Slide 52: Grow CDMO API

    Growth driver: • Grow CDMO API • Further Strengthen CDMO: Leverage GMP manufacturing capabilities for Innovative New Chemical Entities • Custom Manufacturing: Partner with large pharma to manufacture products requiring life cycle management • China plus one strategy: Resilient supply chain through i

  53. Slide 53: Generics

    Generics

  54. Slide 54: Generics Market Growth Drivers and Trends

    Generics Market Growth Drivers and Trends USD Bn ~ 532 Developed Market 19 • US market to grow at 2%, signs of decrease in price reductions ~ 406 15 203 • Non-US market to grow by 5 - 7% 149 India Market 310 242 • India market to grow in excess of 8% • Brand building, in-clinic effectiveness of sale

  55. Slide 55: Non-US international, US and Indian markets

    Non-US international market • Broad therapeutic coverage - CVS, CNS, GI and multi specialty • 1 key markets with triple digit revenue in INR Cr., Build total of 3 - 4 markets (B2B2C) • Global presence in 50+ markets - US, Europe, Canada, Japan, Australia • CMO to few large branded generics customers

  56. Slide 56: Generics quarterly results

    Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y • Q3’FY25 revenue stable YoY • Q3’FY25 EBITDA sharply improved YoY due to Revenue 199 173 200 0% 573 528 (8%) overhead cost savings & profitable product mix. EBITDA (31) 21 30 198% (102) 40 139% EBITDA Margin (%) (15%) 12% 15

  57. Slide 57: Generics FY30 targets

    Revenue : ~2x of FY24 EBITDA Margin : 15% to 17% Revenue : Rs. 729 Cr. EBITDA Margin : Breakeven Revenue : Rs. 775 Cr. Revenue : Rs. 762 Cr. EBITDA Margin : (18%) EBITDA Margin : (30%) FY23 FY24 TTM Dec'24 FY30 57

  58. Slide 58: Launch new products and grow non-US market

    Launch Grow the profitable Build branded new products Non-US international market business • Relaunch dormant ANDAs from • Launch 6 to 8 new products • Build presence in Diabetes, Roorkee and CMO network every year Dyslipidemia and Hypertension • Secure ANDAs (33) approvals • Scale 3 to 4 key market

  59. Slide 59: Proprietary Novel Drugs

    Proprietary Novel Drugs

  60. Slide 60: Precision oral medicines in oncology

    • Develop precision oral medicines with enhanced safety and therapeutic efficacy • Focused on specific set of patients, not responding to other therapies • Low-cost in-house discovery engine to generate drug candidates, validated through partnerships • Guided by world’s leading oncologists from Memo

  61. Slide 61: JBI-802

    • Company sponsored Phase II trial underway Blood Cancer • Highly differentiated for safety and efficacy than peers ET/MPN • Total Addressable Market in US: USD 3.3 Bn. • Investigator led trial under planning Lung Cancer JBI-802 NSCLC • Demonstrated clinical efficacy in two NSCLC patients in phase 1

  62. Slide 62: JBI-802 patient responses

    • Non small cell lung cancer patient progressed to last stage after immunotherapy. Post taking JBI-802 treatment, patient has been doing very well even after two years. Major symptoms have disappeared with confirmed partial response with ~40% tumor reduction • Over 50% shrinkage of the patient’s liv

  63. Slide 63: JBI-778

    Lung Cancer • Company sponsored First-in-human Phase I trial ongoing in India NSCLC with EGFR mutation • Total Addressable Market in US: USD 2.0 Bn. Brain Tumor • High unmet need with no effective treatment option JBI-778 HGG • Total Addressable Market in US: USD 1.7 Bn. Phase I trial underway Head

  64. Slide 64: Proprietary Novel Drugs quarterly results

    • Continue to invest in a calibrated manner in two Particulars ( Rs. Cr.) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y lead programs Revenue 0 0 0 0 0 EBITDA (5) (3) (5) (13%) (23) (14) 37% 64

  65. Slide 65: Clinical readouts and monetization

    • Expect clinical data readouts from CY 2025 to CY 2026 • Explore monetization through licensing or external fund raising 65

  66. Slide 66: Consolidated Q3 FY25 results

    Particulars ( Rs. Cr. ) Q3’FY24 Q2’FY25 Q3’FY25 Y-o-Y 9M'FY24 9M'FY25 Y-o-Y • Q3’FY25 Revenue grew by 9% YoY on the back of growth in revenue across all segments Revenue 1,677 1,752 1,822 9% 4,944 5,306 7% • Q3’FY25 EBITDA increased 11% YoY due to Other Income 36 22 9 54 45 improved performance in C

  67. Slide 67: Net debt and leverage

    Particulars ( Rs. Cr. ) Mar 31, 2024 Dec 31, 2024 • Net Debt / Ebitda continues to improve Net Debt ( On constant currency, Net of DIC ) 2,457 1,654 • USD 125 million voluntary prepayment in YTD FY25, including USD 25 million in Jan’25 Net Debt / Equity 0.46 0.29 Net Debt / EBITDA (TTM) 2.5 1.4 Exch

  68. Slide 68: Sustainability Performance

    Climate B Water B Supply Chain B Achieved 93 percentile Achieved 85 percentile 12,895 patients consulted through 37 % reduction in Specific Greenhouse 23% reduction in Specific Water Jubicare Tele-clinic Gas Emissions v/s FY 19* Consumption v/s FY 19* Sustainability Performance Collaborated with 22%

  69. Slide 69: Business highlights by segment

    Radio Pharmaceuticals : New products and Ruby-Fill® maintaining growth momentum 1 Radio Pharmacies : Industry wide Technetium shortage impacted business, Commercial distribution of PLYARIFY® started 2 Allergy Immunotherapy : Q3’FY25 revenue grew YoY; EBITDA margins have started to improve 3 CDMO Ste

  70. Slide 70: Total income, revenue and EBITDA by segment

    Total Income ( Rs. Cr. ) Q3’FY24 Q2’FY25 Q3’FY25 9M'FY24 9M'FY25 FY24 Revenue (A) 1,677 1,752 1,822 4,944 5,306 6,703 a. Radiopharma 752 820 841 2,184 2,493 3,001 Radiopharmaceuticals 241 251 265 696 778 952 Radiopharmacies 511 568 576 1,488 1,715 2,050 b. Allergy Immunotherapy 161 170 171 491 509 6

  71. Slide 71: FY30 targets: 2x revenue, 23-25% EBITDA margin, zero net debt

    Revenue Reach 2x from FY24 to FY30 EBITDA Margin 23% to 25% by FY30 Net Debt Zero by FY30 RoCE High Teens by FY30 71

  72. Slide 72: Annexure

    Annexure Arvind Chokhany Group CFO, Whole-time Director

  73. Slide 73: Leadership team

    Shyam S Bhartia Hari S Bhartia Priyavrat Bhartia Arjun S Bhartia Chairman Co-Chairman Managing Director Joint Managing Director Arvind Chokhany Shantanu Jha Dr Tushar Gupta Group CFO, Whole-time Director Group CHRO Head - Corporate Strategy 73

  74. Slide 74: Business CEOs

    Harsher Singh Chris Preti Giuliano Perfetti CEO - Jubilant Radiopharma CEO - CDMO Sterile Injectables CEO - CRDMO, Biosys Dr Jaidev Rajpal Kyle Ferguson Dr Syed Kazmi CEO - Jubilant Generics CEO - Allergy Immunotherapy CEO - Jubilant Therapeutics 74

  75. Slide 75: Shareholding pattern

    0.6% 24.8% Promoter and Promoter Group Domestic Institutions 50.7% Foreign Institutions Non - Institutions 17.0% Employee Benefit Trust 7.0% 75

  76. Slide 76: Abbreviations

    Abbreviation Details Abbreviation Details CVS Cardiovascular System MEA Middle East Africa CNS Central Nervous System LATAM Latin America CDMO Contract Development Manufacturing Organization LOE Loss of exclusivity CRDMO Contract Research & Development Manufacturing Organization FDA (US) U.S. Food a

  77. Slide 77: Thanks!

    Thanks!

Jubilant Pharmova — Investor Presentation (April 2025) on 6ix