Eagle Pharmaceuticals, Inc. · OTC:EGRX

Eagle Pharmaceuticals — Investor Presentation (January 2015)

20 slides from Eagle Pharmaceuticals's investor presentation, Jan 12, 2015

  1. Slide 1: January 2015 Investor Presentation

    January 2015 Scott Tarriff, CEO David Riggs, CFO NASDAQ: EGRX

  2. Slide 2: Forward Looking Statements

    Forward Looking Statements 2 This presentation contains certain forward-looking information about Eagle Pharmaceuticals that is intended to be covered by the safe harbor for "forward-looking statements" provided by the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking sta

  3. Slide 3: Eagle Pharmaceuticals

    Eagle Pharmaceuticals Nasdaq: EGRX Specialty pharmaceutical company Differentiated forms of branded injectables Revenues from three products Ryanodex (launched Aug. 2014 in MH) Argatroban Diclofenac/misoprostal Significant near-term commercial opportunities Preparing for 2015 launch of Bendamustine

  4. Slide 4: In-Market Products + Attractive Late Stage Portfolio

    In-Market Products + Attractive Late Stage Portfolio Preclinical Clinical NDA filing Approval In-market Market Opp1 Orphan Drug $99M $43M $75-80M+ $700M+ $700M+ $150M+ $550M $2.7B Bendamustine RTD 30/60 min. admin in 500 mL admixture Bendamustine RTD 10 min. admin in 50 mL admixture Diclofenac/misop

  5. Slide 5: Bendamustine RTD

    Bendamustine RTD Improved formulation of Treanda1 In 500 mL admixture, 30- or 60-minute infusion time (same as Treanda) Tentative approval for NHL received 7/02/14 One patent infringement lawsuit dismissed (‘524), one pending (‘270) ‘270 patent covers lyophilized forms of bendamustine Eagle believes

  6. Slide 6: Bendamustine RTD

    Bendamustine RTD Improved formulation of Treanda1 In 500 mL admixture, 30- or 60-minute infusion time (same as Treanda) Tentative approval for NHL received 7/02/14 One patent infringement lawsuit dismissed (‘524), one pending (‘270) ‘270 patent covers lyophilized forms of bendamustine Eagle believes

  7. Slide 7: Bendamustine RTD in 50mL Admixture Positive Clinical Data

    Bendamustine RTD in 50mL Admixture Positive Clinical Data Open-label, crossover, randomized, blinded Phase I clinical trial in 81 patients Bioequivalence & safety vs. Treanda Met primary endpoint: bioequivalent to Treanda Met safety endpoints: incidence & profile of AEs (infusion-related & general)

  8. Slide 8: Bendamustine RTD Market Opportunity

    Bendamustine RTD Market Opportunity Treanda sales over $700M Preparing for possible 2015 launch Conversion expected due to multiple benefits of our bendamustine RTD in 50mL admixture with 10 minute infusion time Plan to file for unique J-code 1 12 months ended 9/30/2014 sales of $718M, source: Teva

  9. Slide 9: Multiple Benefits of Bendamustine RTD in 50mL Admixture

    Multiple Benefits of Bendamustine RTD in 50mL Admixture Patient Less chair time: 30 or 60 min. reduced to 10 min. Less volume & issues related to 50mL vs. 500mL admixture Nurse Less nursing time required Medical/Patient 90% reduction in NaCl - renal suppressed population Economic Additional patient

  10. Slide 10: Ryanodex for Malignant Hyperthermia

    No change to SOC for MH treatment in over 30 years Often fatal if untreated Ryanodex approved July 22, 2014 Optimized formulation Reduces to 5mL (1 vial) vs. 720 mL (12 vials) for old product Breakthrough change Expected to take over market Protected market position 3 patents issued + 1 filed Orphan

  11. Slide 11: Ryanodex: US Commercial Landscape

    Ryanodex: US Commercial Landscape Ryanodex launched Aug 29, 2014 Small sales force Premium pricing to old formulation Supported by Ryanodex advantages Faster administration Reduced volume Significant reduction of Mannitol (diuretic) Expands addressable market ~$20M $75-80M Ryanodex Premium Pricing O

  12. Slide 12: Ryanodex: US Commercial Landscape

    Ryanodex: US Commercial Landscape All US hospitals required to stock dantrolene ~9,000 outlets MHAUS1 recommends a minimum 36 vials = 3 vials Ryanodex Repurchase required every 2 years Ryanodex advantages = unlikely to revert to old 720mL formulation Early conversions include multiple top-tier hospi

  13. Slide 13: Why Dantrolene?

    Why Dantrolene? MH Exertional Heat Stroke Ecstasy Overdose Duchenne Europe ROW Initial indication: Malignant Hyperthermia Larger markets + Unmet needs Further opportunity for all indications Malignant Hyperthermia is just the tip of the iceberg Rhabdomyolysis

  14. Slide 14: Ryanodex for EHS: Initial Label Expansion Opportunity

    Ryanodex for EHS: Initial Label Expansion Opportunity Exertional Heat Stroke (EHS) Est. 23,000-38,000 cases/year1 A leading cause of student athlete death (US) & non-combat military deaths Similarities to MH Potential for Ryanodex to be first to market for EHS Orphan drug designation for EHS Potenti

  15. Slide 15: Bivalirudin RTU

    Enhanced RTU version of the anticoagulant Angiomax1 Brand sales over $580M 2 Two patents issued; third patent filed 1Q:14 NDA submission targeted for 2Q:15 US launch planned as early as 1Q:16 Very strong non-infringement arguments Different from existing ANDA litigation Bivalirudin RTU 1 Angiomax® (

  16. Slide 16: Pemetrexed

    Pemetrexed Liquid version of Alimta1, a powder cytotoxic API indicated for pleural mesothelioma & NSCLC No reconstitution No dilution Less exposure to cytotoxic vapors for healthcare staff $2.7B global market opportunity2 Expect to launch with generics (2017-21) 1 Alimta® (pemetrexed) (Eli Lilly & C

  17. Slide 17: US Patents Longevity and Orphan Drug

    US Patents Longevity Orphan Drug FDA Action Issued Filed Argatroban 2 1 Sept 2027 In-market Ryanodex (dantrolene): MH 3 1 Jul 2022- Jul 2025 US EU In-market Bendamustine RTD: NHL & CLL 2 3 Jan 2031- Mar 2033 US 500mL Tentative Approval 7/2/14 50mL meeting w. FDA 12/14 Ryanodex: Heat stroke/EHS 1 Feb

  18. Slide 18: Achievements Since Jan:14 and Near-term Milestones

    Achievements Since Jan:14 Near-term Milestones Ryanodex® NDA filed: MH Mar:14 Type C meeting with FDA Mar:15 Patent issued: heat stroke 1Q:14 Initiate clinical study: EHS Sept:15 FDA approval: MH Jul:14 File with EMA: MH 4Q:15 US Launch: MH Aug:14 ODD from EMA: MH Nov:14 Bendamustine Tentative appro

  19. Slide 19: Investment Considerations

    Investment Considerations Large market opportunity in injectable products space Revenues from three in-market products Near term product launch opportunities with high margins 3 Orphan Drugs: Ryanodex EHS & MH and bendamustine 50mL admixture Strong IP portfolio to protect market position: 12 patents

  20. Slide 20: Eagle Pharmaceuticals, Inc.

    EAGLE PHARMACEUTICALS, INC. January 2015

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