Scilex Holding Company · NASDAQ:SCLX

Scilex — Investor Presentation (January 2025)

57 slides from Scilex's investor presentation, January 2025

  1. Slide 1: Innovative Leader in Non-Opioid Pain Therapeutics/Obesity/Neurodegenerative/Cardiometabolic Disease

    Innovative Leader in Non-Opioid Pain Therapeutics/Obesity/ Neurodegenerative/Cardiometabolic Disease

  2. Slide 2: Safe Harbor Statements Forward-Looking Statements

    Safe Harbor Statements Forward-Looking Statements Certain statements contained in this corporate presentation (this “Presentation”), along with certain statements that may be made by management of Scilex Holding Company (together with its subsidiaries, “Scilex”) orally in presenting this material, a

  3. Slide 3: Scilex Holding Company Structure

    Scilex Holding Company Structure Scilex Holding Company Ticker Symbol “SCLX” SCLX Stock Acquisition JV LLC (SCLX Shares: 60MM common Scilex Pharmaceuticals Inc. Scilex Bio, Inc., majority and 29MM Semnur Pharmaceuticals Inc. ZTlido®, GLOPERBA®, owned by Scilex Holding preferred shares) SP-102 (SEMDE

  4. Slide 4: Denali SPAC Transaction

    Denali SPAC Transaction • On August 30, 2024, Semnur Pharmaceuticals, Inc. (“Semnur”), a wholly owned subsidiary of Scilex Holding Company (Nasdaq: SCLX, “Scilex”), and Denali Capital Acquisition Corp. (Nasdaq: DECA, the “SPAC”) announced the signing of an agreement and plan of merger for a proposed

  5. Slide 5: Scilex Pharmaceuticals Exploring a Spinoff or IPO

    Scilex Pharmaceuticals Exploring a Spinoff or IPO • Scilex Holding Company Announces that its Board of Directors has Authorized Management to Explore Ways to Maximize the Value of its Wholly Owned Subsidiary, Scilex Pharmaceuticals Inc., including by way of conducting a spinoff or public listing of

  6. Slide 6: Scilex Bio Obesity/Neurodegenerative/Cardiometabolic Disease

    Scilex Bio Obesity/ Neurodegenerative/ Cardiometabolic Disease

  7. Slide 7: KDS2010 (Tisolageline)

    KDS2010 (Tisolageline) • Familiar old drug class – Inhibitor of Monoamine Oxidase (B) • New generation • Highly selective, highly potent, BBB permeable, and reversible inhibitor • New anti-obesity mechanism discovered • Suppresses aberrant GABA (gamma-aminobutyric acid) production in reactive astroc

  8. Slide 8: Publications

    Publications SCILEX’ HOLDING COMPANY + Nature Medicine GABA from reactive astrocytes impairs memory in mouse models of Alzheimer's disease 2014. 6.29. * Science Advances Newly developed reversible MAO-B inhibitor circumvents the shortcomings of irreversible inhibitors in Alzheimer's 2019. 3. 20. + C

  9. Slide 9: KDS2010 Phase 1 Clinical Program Completed

    KDS2010 Phase 1 Clinical Program Completed • KDS2010 well tolerated and safe for single dose (30 to 960 mg) and repeated dosing over 7 days (60 to 480 mg). • Adequate pharmacokinetics for once-daily dosing in the range of 60 to 480 mg for repeat dosing. • No food effect on pharmacokinetics, allowing

  10. Slide 10: Scilex Pharmaceuticals

    Scilex Pharmaceuticals 960 San Antonio Rd, Palo Alto CA 94303 Wholly Owned Subsidiary of Scilex Holding Company (NASDAQ: SCLX)

  11. Slide 11: Key Achievements

    Key Achievements • Fifth year company anniversary • ZTlido - #1 prescribed branded non-opioid analgesic by the pain specialist • Over 1MM patients treated with ZTlido since launched • ~90% of patients are satisfied with ZTlido treatment • 88% patients felt they could do more when on ZTlido treatment

  12. Slide 12: Scilex Business Opportunity Highlights

    Scilex Business Opportunity Highlights • In US 50m patients live with chronic pain – A billion adults suffer from acute or chronic pain globally • With opioid pandemic, medical community and regulatory agency seeking non-opioid pain options • Scilex has three commercial products on the market and of

  13. Slide 13: Innovative Non-Opioid Pain Therapeutics

    Innovative Non-Opioid Pain Therapeutics KEY PROGRAMS PRECLINICAL PHASE 1 PHASE 2 PHASE 3 / PIVOTAL APPROVED IP MILESTONES / KEY COMMENTARY ZTlido® Platform Phase 3 Program IND Phase 1 Phase 2 NDA Approved Upcoming Milestones (1.8% lidocaine topical system Approved for the treatment of Postherpetic N

  14. Slide 14: Investment Highlights

    Investment Highlights  3 FDA approved Non-Opioid Acute and Chronic Pain Management Products  Worldwide Commercial Rights to Most Product Candidates  Strong Proprietary Platform with High Barriers to Entry  Established Reimbursement Access  Blockbuster Pipeline With Limited Capital Required for

  15. Slide 15: ZTlido

    ZTlido (1.8% lidocaine topical system equivalent to 5% lidocaine for the treatment of Postherpetic Neuralgia-PHN related pain)

  16. Slide 16: ZTlido Commercialization Success

    ZTlido Commercialization Success 16

  17. Slide 17: The Gabapentinoid Market Is Massive

    Confidential, not for distribution The Gabapentinoid Market Is Massive Gross sales of $370M would equate to ~1M ZTlido TRx The Neuropathic Pain Gabapentinoid market is an order of magnitude bigger than the Lidocaine patch market 88M Annualized ~44M Gabapentinoid Neuropathic 1+M scripts pain Rx ZTlid

  18. Slide 18: ZTlido 1.8% (FDA approved for relief of PHN pain)

    ZTlido® 1.8% (FDA approved for relief of PHN pain) 1  Lidocaine Patch Market Overview - +4.6mm prescriptions in 2022 - +169mm prescription lidocaine patches sold in the U.S. in 20221 2  Benefits versus Other Lidocaine Patches - Superior adhesion compared to other lidocaine patches head-to-head stu

  19. Slide 19: The ZTlido New Campaign as the ideal add-on to Gabapentinoids

    The ZTlido New Campaign as the ideal add-on to Gabapentinoids Designed to allow the brand to achieve its true potential by repositioning from Adhesion to Efficacy ZTlido is uniquely capable of optimizing gabapentinoids – doubling efficacy without the baggage/side effects of other analgesic options (

  20. Slide 20: ZTlido Market Access Update

    ZTlido Market Access Update ZTlido Covered Lives Overview Key Players - Preference 350 308 21 ZTlido Preferred 300 69 250 218 State of California (MediCal) Lidocaine Preferred 200 150 ZTlido Preferred 100 50 ZTlido Preferred 0 Total Lives Later In-Negotiations Covered Negotiations 20

  21. Slide 21: The "New ZTlido" Opportunity: Summary

    The “New ZTlido” Opportunity: Summary • Relaunching ZTlido in a 10X market potential • The Unmet Need in the neuropathic pain market/PHN – efficacy without side effects – is high. • HCP satisfaction with Gabapentinoids (gabapentin and pregabalin) is low. • ZTlido is uniquely capable of optimizing Ga

  22. Slide 22: ZTlido Partnership Ex-U.S.

    ZTlido Partnership Ex-U.S. • Established Middle East and NA partnership, filngs underway in UAE, Saudi Arabia and North Africa, launched planned for 2025 • On July 17, 2024, Scilex Holding Company Announces Collaboration to Leverage ACEA Therapeutics’ R&D Expertise and Local Market Connections to Su

  23. Slide 23: ZTlido LTC Opportunity

    ZTlido® (lidocaine topical system) 1.8% LTC Opportunity

  24. Slide 24: Non-Opioid Pain Opportunity in LTC

    Non-Opioid Pain Opportunity in LTC • Long Term Care Skilled Nursing Facilities are an untapped opportunity for Scilex, CMS estimates there are 1.5 million residents in certified facilities across the US1 85.1% of Skilled Nursing patients are aged 65 and over, with 67.7% being women2 Chronic pain pre

  25. Slide 25: Key Players In Skilled Nursing Facilities

    Key Players In Skilled Nursing Facilities Consultant Pharmacist (Oversees all medications & completes chart reviews) Medical Payers Director (Processing & (Approves all formulary) Long Term decisions & formulary) Care Facilities Director of Prescribers Nursing (Medication (Administrative& decisions)

  26. Slide 26: Long Term Care Key Players

    Long Term Care Key Players Government (CMS) • Medicare • Medicare Advantage Programs (through Commercial Payers) • Medicaid • Dual eligible patients (Medicaid & Medicare eligible) Commercial Payers • United Healthcare and Humana represent two large Medicare Advantage plans Pharmacy Distribution Orga

  27. Slide 27: LTC Key Influencers - GPO's and Pharmacy Providers

    LTC Key Influencers - GPO’s and Pharmacy Providers GPO’s MHA (Managed Healthcare Associates), GeriMed, Innovatix/Premier, Asembia (more in Specialty space) and Vizient (Works thru GeriMed contract – Pull Thru main target once GeriMed contracted). Pharmacy Providers Omnicare – (Owned by CVS) diminish

  28. Slide 28: LTC Associations – Influence Pain Management

    LTC Associations – Influence Pain Management Associations • ASCP (American Society of Consultant Pharmacist), • GAPNA (Gerontological Advanced Practice Nurses Association), • PALTC (Post- Acute LTC Medical Directors), • AAPA (American Association of Physician Assistants), • AAPACN (American Associat

  29. Slide 29: SP-103 Phase 2

    Next-Generation, Triple Strength Formulation of ZTlido 1.8% SP-103 Phase 2 Next-Generation, 5.4% Lidocaine Topical System  3x drug load (108 mg vs 36 mg lidocaine)  Superior adhesion and drug formulation  Triple strength localized dose of lidocaine efficiency with only 36mg of lidocaine  Expecte

  30. Slide 30: Neck Pain Market Overview

    Neck Pain Market Overview Neck pain, or cervicalgia, is one of the most common pain presentations in U.S. and the 4th leading cause of disability 52.9M adults suffer from Neck Pain in the U.S. Prevalence of Neck Pain is estimated at >20% of adult population Neck pain was responsible for job absences

  31. Slide 31: Elyxyb (celecoxib) oral solution

    Elyxyb (celecoxib) oral solution (Acute Treatment of Migraine)

  32. Slide 32: Elyxyb Launched in USA in 2023

    Elyxyb Launched in USA in 2023 32

  33. Slide 33: Approximately 39M People with Migraine in the US

    Approximately 39M People with Migraine in the US Some patients may receive both acute as well as preventive treatment Source: Prevalence by Migraine Research Foundation, 2021; Epidemiology data by DRG 33

  34. Slide 34: Elyxyb Promotion Materials

    Elyxyb Promotion Materials 34

  35. Slide 35: ELYXYB (Celecoxib) Oral Solution Episodic Migraine Treatment

    ELYXYB (Celecoxib) Oral Solution Episodic Migraine Treatment 35

  36. Slide 36: Elyxyb Efficacy Comparison to CGRP Inhibitors

    Elyxyb Efficacy Comparison to CGRP Inhibitors Post-hoc Indirect Comparative Analysis • Gepants are known to have a slow onset of action • At 1 hour, 5x more patients on ELYXYB will be pain free vs Ubrelvy® • At 2 hours postdose, about 2x as many patients on ELYXYB will be pain free vs. Nurtec® • ELY

  37. Slide 37: The US Migraine Market Is Projected To Grow By 195%

    The US Migraine Market Is Projected To Grow By 195% Between 2021 to 2026 • Scilex current forecast growth of more than 3X in 2024 compared to 2023. Source: Evaluate; Above data includes both acute and preventative therapies; Data refreshed in January 2022 37

  38. Slide 38: Elyxyb Acute Pain Opportunity: Market Size

    Elyxyb Acute Pain Opportunity: Market Size 91.6M 45.8M (Acute Pain (Diagnosed Prevalence) Prevalence) 20.7M (Acute Pain - sNDA filing planned in 2025 Treated w/ Rx) >20M U.S. Patients Large market opportunity for Elyxyb in Acute Pain Confidential, not for distribution 38

  39. Slide 39: Elyxyb Acute Pain Opportunity: Unmet Needs

    Elyxyb Acute Pain Opportunity: Unmet Needs Key Unmet Needs in Acute Pain: Fast onset Need for safer and more effective treatments Non-Opioid alternatives Confidential, not for distribution 39

  40. Slide 40: Gloperba

    Gloperba (colchicine USP) oral solution (For the prevention of painful gout flares in adults)

  41. Slide 41: Gloperba Launched in USA in June 2024

    Gloperba Launched in USA in June 2024 41

  42. Slide 42: Gloperba Launched in June 2024

    Gloperba Launched in June 2024 Scilex Holding Company announces the U.S. FDA has approved the sNDA for commercial manufacturing of Gloperba® which was launched in the US in the week of June 10th 2024. • Gloperba® is the first and only liquid oral version of the anti-gout medicine colchicine indicate

  43. Slide 43: Target Patients For Gloperba Today (excluding Cardiovascular)

    Target Patients For Gloperba Today (excluding Cardiovascular) • Patients with CKD Stage 3/4/5: 6 million patients • Patients with GI tolerability issues: 1 million patients • Patients at risk of drug-to-drug interaction (DDI) • Patients who have difficulty swallowing • Cardiovasular up to 6.5 millio

  44. Slide 44: Rheumatologists indicated they would use Gloperba in patients with CKD 3-5 and GI

    Rheumatologists indicated that they would use Gloperba in patients with CKD 3-5 and GI Sensitivity Over 70% of gout patients suffer from CKD Number of Physicians who Expect to Prescribe GLOPERBA in Different Types of Patients Rheumatologist (n=17) CKD Stage 3-5 13 GI Intolerance / Issues 10 Swallowi

  45. Slide 45: Rheumatologists showed high willingness to prescribe Gloperba

    Rheumatologists showed high willingness to prescribe Gloperba, and even do Prior Authorization Motivation to Prescribe Gloperba Likelihood to do a PA for Gloperba HIGH: 6.1/7 (Ave.) MODERATE: 5.4/7 (Ave.) Current Level • PAs are a hassle that rheumatologists prefer not to do. • Offers precise dosing

  46. Slide 46: Gloperba reduced dosing offers value for money

    Gloperba reduced dosing offers value for money Colchicine TABLET (mg) to GLOPERBA Liquid (mL) Conversion Table The WAC price of Gloperba is $595 for a 150mL bottle. Colchicine (mg) GLOPERBA (mL) -Value for $: Will last for 60 days for patients 0.12 mg 1.0 mL with Severe renal impairment (CKD 4) - 0.

  47. Slide 47: Gloperba solves for the Unmet Need HCPs have stated

    Gloperba solves for the Unmet Need HCPs have stated For internal use only. Not to be shown to healthcare professionals. 47

  48. Slide 48: Semnur Pharmaceuticals

    Semnur Pharmaceuticals 960 San Antonio Rd, Palo Alto CA 94303 Wholly Owned Subsidiary of Scilex Holding Company (NASDAQ: SCLX)

  49. Slide 49: SP-102 Market Opportunity

    SP-102 Market Opportunity Developing SP-102 as a non-opioid injectable therapeutic for low back pain Novel viscous gel formulation, optimized for epidural injection Novel biocompatible excipient enables extended local effect On track to be the first and only FDA-approved epidural steroid product Cur

  50. Slide 50: SEMDEXA (SP-102) On-Track to be the First Product Approved to Treat Sciatica

    SEMDEXA (SP-102) On-Track to be the First Product Approved to Treat Sciatica • SP-102 is a preservative free, surfactant free and particulate free viscous gel formulation of dexamethasone for sciatica (lumbosacral radicular pain). • Extended local effect provides durable pain relief and significant

  51. Slide 51: SP-102 Differentiated Product Profile & Positioning

    SP-102 Differentiated Product Profile & Positioning 1 51

  52. Slide 52: SEMDEXA – Broad Potential for Life Cycle Management

    SEMDEXA – Broad Potential for Life Cycle Management 1 Physicians indicated there is potential opportunity for spontaneous use of SEMDEXA outside of lumbar radiculopathy which could represent an additional upside of ~50-200%* over LR 2 Additional Uses  Carpel Tunnel  Hip and Knee Replacements  Tri

  53. Slide 53: Scilex Holding Employee Organizational Chart

    Scilex Holding Employee Organizational Chart

  54. Slide 54: Scilex Commercial Organizational Structure

    Scilex Commercial Organizational Structure Chief Commercial Officer Analytics & Head of Market Director Sales National Sales Marketing Director Sales Ops Forecasting Director Access Training Director Director Account Managers Sr PM + Marketing Senior Analyst Regional Field Senior Analyst Regional Bu

  55. Slide 55: National Map

    National Map Please note that images do not represent the actual size

  56. Slide 56: Management Team

    Management Team Jaisim Shah Henry Ji, PhD Dmitri Lissin, MD Steve Lincoln Chief Executive & President Executive Chairman Chief Medical Officer GC and Chief Compliance Officer  25+ years of management  25+ years of experience in the  20+ years in clinical development in  20+ years in industry, wi

  57. Slide 57: Nasdaq (November 11, 2022)

    Nasdaq (November 11, 2022) 57

Scilex Holding Company — Investor Presentation (January 2025) on 6ix