Delcath Systems, Inc. · NASDAQ:DCTH

Delcath Systems — Investor Presentation (March 2015)

27 slides from Delcath Systems's investor presentation, Mar 10, 2015

  1. Slide 1: Investor Presentation

    Exhibit 99.1 Investor Presentation (NASDAQ: DCTH) March 2015

  2. Slide 2: Forward-looking Statements

    Forward-looking Statements This presentation contains forward-looking statements, within the meaning of the federal securities laws, related to future events and future financial performance which include statements about our expectations, beliefs, plans, objectives, intentions, goals, strategies, a

  3. Slide 3: About Delcath Systems

    About Delcath Systems • A specialty pharmaceutical and medical device oncology company with a principal therapeutic focus on the treatment of primary liver cancer and other cancers that have metastasized to the liver • Proprietary system isolates the liver from circulation, delivers a substantially

  4. Slide 4: Investment Highlights

    Investment Highlights • Late-stage asset – demonstrated clinically meaningful efficacy in more than 600 procedures and multiple tumor types • Active clinical program – initiating global Phase 3 study in ocular melanoma; HCC/ICC Phase 2 program ongoing • Unique, highly differentiated solution – orpha

  5. Slide 5: 2014-2015 Milestones

    2014-2015 Milestones 2014 Accomplishments ü Phase 2 HCC trial open and first patient treated ü 100th patient treated in Europe (commercial and clinical) ü Positive efficacy data from three institutions presented at ESSO 2014 ü Product revenue increased 118% Y/Y to $1.1 million ü Cash burn reduced by

  6. Slide 6: The Liver: A Life-Limiting Organ

    The Liver: A Life-Limiting Organ • Cancers of the liver remain a major unmet medical need o Large global patient population – approximately 1.2 million* patients diagnosed annually with primary or metastatic liver cancer o The liver is often the life-limiting organ for cancer patients and one of the

  7. Slide 7: Existing Liver Cancer Treatments Landscape

    Existing Liver Cancer Treatments Landscape Treatment Advantages Disadvantages – Non-invasive – Systemic toxicities Systemic – Repeatable – Limited efficacy in liver – Invasive/limited repeatability Regional – Therapeutic effect – Multiple treatments are (e.g., Isolated Hepatic Perfusion) – Targeted

  8. Slide 8: Our Solution: Whole Organ-Focus Disease Control

    Our Solution: Whole Organ-Focus Disease Control • Our proprietary system isolates the liver circulation, delivers a high concentration of chemotherapy (melphalan) and filters most of the chemotherapy out of the blood prior to returning it to the patient • The procedure typically takes approximately

  9. Slide 9: The Melphalan Hepatic Delivery System (HDS)

    The Melphalan Hepatic Delivery System (HDS) Liver Isolated Via Double Balloon Melphalan Infused Directly Into Liver Blood Exiting The Liver Filtered By Catheter In IVC Via Catheter In Hepatic Artery Proprietary Extra-corporeal Filters • Device designed to administer high-dose chemotherapy to the liv

  10. Slide 10: Melphalan Dosing & Background

    Melphalan Dosing & Background Type Dosing (mg/kg) Multiple Myeloma (label) 0.25 Chemoembolization 0.62 Surgical Isolated Hepatic Perfusion (IHP) 1.50 Myeloablation 2.50-3.50 Chemosaturation (PHP) 3.00 • Well-understood, dose-dependent, tumor-preferential, alkylating cytotoxic agent that demonstrates

  11. Slide 11: Total Available EU & U.S. Market Opportunity

    Total Available EU & U.S. Market Opportunity Annual Potential Cancer Type Annual Incidence1 Eligible Pts2 Revenue per Patient3 Market Opportunity (millions) Ocular Melanoma (OM) 5,700-8,600 2,600-4,300 $40,000-$50,000 $104-$215 Cholangio Carcinoma (ICC) 11,500 6,500 $40,000-$50,000 $260-$330 Hepatoc

  12. Slide 12: Clinically Differentiated Results

    Clinically Differentiated Results • Phase 1, 2 and 3 trials produced positive results in multiple histologies • Melanoma Liver Mets o Positive Phase 3 results in hepatic metastatic melanoma o n=93 (90% ocular melanoma, 10% cutaneous melanoma) • Neuroendocrine Tumor (NET) Liver Mets o mNET cohort in

  13. Slide 13: Clinical Development Program Overview

    Clinical Development Program Overview • Initiating global Phase 3 trial 2H 2015 in Ocular Melanoma (OM) Liver Mets • Establish proof-of-concept in Hepatocellular Carcinoma (HCC) and Intrahepatic Cholangiocarcinoma (ICC) o Commenced global Phase 2 program in HCC in 2014 o Expanding program to include

  14. Slide 14: Clinical Development Program Detail

    Clinical Development Program Detail Trials Tumor Objectives § Global Phase 3 trial to start 2H-2015 Phase 3 Pivotal Trial OM liver mets § Primary endpoint: Overall Survival (OS) § Believed to be fastest pathway to NDA approval in the U.S. § Protocol 201 (U.S. only) § Safety, efficacy of melphalan/HD

  15. Slide 15: OM Metastases Rationale

    OM Metastases Rationale • OM has high incidence of liver metastases o Up to 90% of patients with metastases will have liver involvement o Life expectancy of approximately 6 months o 5,700 - 8,600 cases of OM liver metastases diagnosed in U.S. and EU annually • Clear efficacy signal seen in prior Pha

  16. Slide 16: Previous Ocular Melanoma Mets Phase 3 Results

    Previous Ocular Melanoma Mets Phase 3 Results Hepatic Progression Free Survival (hPFS) Overall Progression Free Survival (Investigator) Proportion of patients surviving Proportion of patients surviving 1.0 1.0 3.8 mo Chemosaturation (CS-PHP) 5.3 mo Chemosaturation (CS-PHP) 0.8 0.8 Best alternative c

  17. Slide 17: ICC Rationale

    ICC Rationale • Significant market opportunity in U.S. and EU o ~15% of new HCC cases diagnosed annually o ~90% of patients are not suitable for surgical resection o ~20-30% are candidates for focal interventions o Efficacy signals from early commercial uses in EU • Unmet medical need – Delcath will

  18. Slide 18: HCC Rationale

    HCC Rationale • Significant opportunity in the U.S. and EU o HCC most common primary cancer of the liver o ~76,000* cases diagnosed annually • Large unmet medical need in first-line therapy o Only one approved systemic therapy in the U.S., EU and certain Asian markets o ~90% of patients not candidat

  19. Slide 19: Prior FDA Experience

    Prior FDA Experience • New Drug Application (NDA) submitted August 2012 seeking indication in OM liver metastases with first-generation filters and procedure • ODAC meeting in May 2013 o Efficacy shown with statistical significance o Negative vote due to benefit/risk analysis o Complete FDA & Delcat

  20. Slide 20: Risks Observed in Previous Clinical Program

    Risks Observed in Previous Clinical Program • Risks observed with prior product and procedure protocol • Integrated safety population of patients showed risks associated with melphalan/HDS included: o 4.1% incidence of death due to adverse reactions o 4% incidence of stroke o 2% reported incidence o

  21. Slide 21: Safety Improvements Implemented

    Safety Improvements Implemented • New generation filter o Improve filter efficiency and consistency • Vasopressors and methylprednisolone o Reduce cardiovascular risk • Prophylactic transfusions and growth factors o Reduce risk of myelosuppression • Intra-arterial nitroglycerin o Prevent hepatic art

  22. Slide 22: Positive Developments

    Positive Developments • Improved device and procedure since prior trials o >180 treatments with improved device and procedure in U.S. and EU o Many issues raised at ODAC have not been reported • Current device/procedure permitting multiple treatment cycles • Recent scientific presentations at ESSO f

  23. Slide 23: European Commercial Activity

    European Commercial Activity CHEMOSAT® Hepatic Delivery System •Approved as Class IIb Medical Device; kit supplied without melphalan •Broad indication for intra-hepatic administration of melphalan hydrochloride and subsequent filtration of the venous blood return •>160 commercial procedures performe

  24. Slide 24: CHEMOSAT Commercial Treatments in Europe

    CHEMOSAT® Commercial Treatments in Europe Multiple Tumor Types Treated Since EU Launch Treatments/Re-treatments Increasing 24 DELCATH SYSTEMS, INC

  25. Slide 25: Cash & Capital Resources

    Cash & Capital Resources Cash & Cash Equivalents $20.5 million at December 31, 2014 Debt None ATM Program1 $40 million available at December 31, 2014 Shares Outstanding 12.2 million (14.5 million fully diluted3) at February 17, 2015 1) Subject to market conditions and certain limitations 2) Fully di

  26. Slide 26: In Summary

    In Summary Melphalan Hydrochloride for Injection for use with the Delcath Hepatic Delivery System (Melphalan/HDS) • Cancers of the liver remain a multibillion-dollar unmet medical need • Unique, highly differentiated solution • Late-stage asset in U.S., early commercial activity EU • Compelling emer

  27. Slide 27: 2015 DELCATH SYSTEMS, * DELCATH

    © 2015 DELCATH * DELCATH SYSTEMS, SYSTEMS, INC INC. ALL RIGHTS RESERVED Delcath and CHEMOSAT are registered trademarks of Delcath Systems, Inc.

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