Citius Pharmaceuticals, Inc. · NASDAQ:CTXR

Citius Pharmaceuticals — Investor Presentation (January 2021)

42 slides from Citius Pharmaceuticals's investor presentation, Jan 11, 2021

  1. Slide 1: Citius Pharmaceuticals Corporate Presentation Winter 2020-21

    Citius Pharmaceuticals, Inc. Corporate Presentation Winter 2020 - 21 NASDAQ: CTXR

  2. Slide 2: Disclaimer

    2 NASDAQ: CTXR This presentation has been prepared by Citius Pharmaceuticals, Inc. (the “Company”) for informational purposes only and not for any other purpose. Nothing contained in this presentation is, or should be construed as, a recommendation, promise or representation by the Company or any di

  3. Slide 3: Company Overview

    3 NASDAQ: CTXR Olympic Motto: “ Citius , Altius, Fortius ” ( Faster , Higher, Stronger) Company Overview Four Active Programs with a Late Stage Lead Asset Mino - Lok in late Phase 3; favorable review received for Futility Analysis by Data Monitoring Committee (12/2019); favorable review for safety a

  4. Slide 4: Management

    4 NASDAQ: CTXR Management Leonard Mazur, Director and Executive Chairman • Founder/co - founder of: Genesis, Triax , Akrimax , and others Myron Holubiak, Director, CEO and President • Former President of Roche Laboratories, Inc. Jaime Bartushak, EVP, Chief Financial Officer • Over 20 years experienc

  5. Slide 5: Unique Pipeline in Progressive Stages

    5 NASDAQ: CTXR Program Estimated Market (Worldwide) Preclinical Phase I Phase II Phase III Mino - Lok® Treat CVC Infections > $1.5B CITI - 002 (Halo - Lido) Rx Therapy for Hemorrhoids > $2B CITI - 101 (Mino - Wrap) Prevent Infections Associated with Breast Implants > $400M CITI - 401 ( i MSC ) Treat

  6. Slide 6: Lead Product: Mino-Lok

    LEAD PRODUCT Minocycline/EDTA/Ethanol Antibiotic Lock Therapy for Salvaging Catheters That Cause Bloodstream Infections Mino - Lok®

  7. Slide 7: Biofilm Formation Protects Colonies

    7 Biofilm Formation Protects Colonies • Pathogens attach to the surface of the lumen in a central venous catheter and form colonies. • Colonies grow and exude a fibrous glycocalyx that protects the organisms from antibiotics, even when shown to be sensitive in vitro. Micrograph of Biofilm in Central

  8. Slide 8: Infection Rates and Poor SOC Lead to Death & Morbidity

    8 NASDAQ: CTXR BUT Infection Rates + Poor SOC Leads to Death & Morbidity Infections are Common & Dangerous Of the 7,000,000 CVCs used annually in US, up to 472,000 become infected leading to serious, life threatening infections called CRBSI/CLABSI. 1 These infections are associated with 12 - 25% mor

  9. Slide 9: Remove and Replace Procedures Are Invasive and Costly

    9 NASDAQ: CTXR R&R procedures are invasive and discomforting to patient. R&R Procedures are costly and usually require additional hospital stay. Complications include infection, thrombosis, occlusion, and mechanical complications. • Infectious complications are reported to occur in 5% to 26% of pati

  10. Slide 10: Locking a Central Venous Line with Mino-Lok

    10 NASDAQ: CTXR Locking a Catheter is a Standard Operating Procedure 1. Using Mino - Lok does not require any novel methodologies. 2. Any RN or LPN or Technician can perform the procedure. 3. There is no change in normal workflow and does not require exceptional training. 4. The patient does not exp

  11. Slide 11: Phase 2b Trial Results

    11 NASDAQ: CTXR Phase 2b Trial Results Parameter Mino - Lok Arm N ( % ) Control Arm N ( % ) Patients 30 (100%) 60 (100%) Cancer Type - Hematologic 20 (67) 48 (80) - Solid tumor 10 (33) 12 (20) ICU Admission 4 (13) 4 (7) Mech. Ventilator 3 (10) 0 (0) Bacteremia - Gram+ 17 (57)* 32 (53) - Gram - 14 (4

  12. Slide 12: Mino-Lok Phase 3 Pivotal Trial Design

    12 NASDAQ: CTXR Active Arm (n=72) Mino - Lok® Solution Control Arm (n=72) Antibiotic Lock Patients with CRBSI/CLABSI (n~ 144) R Multi - center, randomized, open label, blinded assessor, active control superiority study (80% powered) Futility Performed at 35 - 40 Events and 60 - 70 Events for Superio

  13. Slide 13: Time-To-Catheter Failure Trial Design

    Mino - Lok® Time - To - Catheter Failure Trial Design 0 10 20 30 40 50 60 70 80 90 100 0 10 20 30 40 50 60 Catheter Survival (%) Time (days) Kaplan - Meier Model ALT MLT 21 vs. 38 Day Difference in Median Number of Catheter Failures 13

  14. Slide 14: Mino-Lok Development Plan

    14 NASDAQ: CTXR 2015 2016 2017 2018 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Pivotal Phase 3 ALT Study 2019 Q1 Q2 Q3 Q4 2020 Q1 Q2 Q3 Q4 2021 Q1 Q2 Q3 Q4 First Patient In Interim Data Safety/Efficacy Analysis FDA Interim Mtg. FDA Review Mtg. Commercial Preparation Phase 2 FDA EOP2 Meeting Reg

  15. Slide 15: Regulatory Protection

    15 NASDAQ: CTXR Regulatory Protection Qualified Infectious Disease Product (US) • Eligibility for Fast Track Status, enables frequent communication and collaboration with FDA; • Priority Review, reduces the NDA review time from 12 to 6 months; and, • Market Exclusivity, grants an additional 5 years

  16. Slide 16: Competitive Landscape

    16 NASDAQ: CTXR Company/Source Product/Components Status Features/Weaknesses CorMedix DefenCath TM ( Neutrolin ®) taurolidine, citrate, heparin NDA accepted by the FDA in August 2020 PDUFA date 2/28/2021 Available in Europe (CE Mark) Prevention only Anti - infective only being used in prophylaxis No

  17. Slide 17: Mino-Lok Summary

    17 NASDAQ: CTXR Mino - Lok® (minocycline/disodium EDTA/ethyl alcohol) Treats catheter - related blood stream infections (CRBSIs). Penetrates biofilm, eradicates bacteria and salvages infected, indwelling vascular catheters while providing anti - clotting properties. Salvages central venous access in

  18. Slide 18: NoveCite induced Mesenchymal Stem Cells (i-MSCs)

    NoveCite induced Mesenchymal Stem Cells (“ i - MSCs”)

  19. Slide 19: Citius, Novellus and NoveCite

    19 Citius Pharmaceuticals, Inc. • late - stage specialty pharmaceutical company • critical care products (anti - infectives and cancer care) • Mino - Lok, Mino - Wrap, and Halo - Lido. NASDAQ (CTXR) Novellus Therapeutics • pre - clinical stage biotechnology company • patented non - immunogenic mRNA

  20. Slide 20: NoveCite i-MSC Unique Advantages

    NoveCite i - MSC Compelling Unique Advantages 20 • Novellus mRNA cell reprogramming efficiently creates i - PSC cells ( i - PSCs are an ideal building - block for cell - based therapies) • Clonal i - PSC master cell bank is created – no batch - to - batch variation and footprint - free (no viral vec

  21. Slide 21: Proprietary mRNA Technology – Non-Immunogenic

    Proprietary mRNA Technology – Non - Immunogenic Ribolog Œ evades the innate immune system and is recognized by the ribosome as mRNA, resulting in no immunogenicity, high protein expression and ability for repeat dose 21 Novellus’s RiboLog Ρ Native mRNA is recognized by the innate immune system so is

  22. Slide 22: i-MSC Production Process & Proof of MSCs

    i - PSCs Day 0 Induction medium Day 4 MSC medium Day 6 Passage Day 9 Passage Day 13 Passage Day 19 Passage Day 26 Passage Day 29 Passage i - MSCs i - MSC Advantages: Production in 30 Days • 6 days of 5 non - immunogenic mRNAs encoding reprogramming factors • Mutation - free, extensively characterize

  23. Slide 23: i-MSCs Advantages: Greater Expansion Potential

    i - MSCs Advantages: Greater Expansion Potential 23 Growth Curve Telomere Length i - MSCs exhibit greater expansion potential – mRNA process restores telomeres to yield >70 population doublings “BM - MSCs” = bone marrow - derived MSCs *Data on file (Novellus) BM - MSCs

  24. Slide 24: NoveCite i-MSC Summary

    NoveCite i - MSC Summary 24 • Novellus mRNA cell reprogramming efficiently creates i - PSC cells ( i - PSCs are an ideal building - block for cell - based therapies) • Clonal i - PSC master cell bank is created – no batch - to - batch variation and footprint - free (no viral vectors) • Rapid product

  25. Slide 25: NoveCite i-MSCs: ARDS in COVID

    NoveCite i - MSCs: ARDS in COVID - 19 SARS - CoV - 2 Severe acute respiratory syndrome coronavirus 2 25

  26. Slide 26: Acute Respiratory Distress Syndrome (ARDS)

    ARDS Lung Normal ARDS a type of respiratory failure characterized by rapid onset of widespread inflammation and fluid accumulation in the lungs. ARDS impairs the lungs’ ability to exchange oxygen for carbon dioxide Symptoms includes shortness of breath, rapid breathing, and bluish skin coloration; f

  27. Slide 27: i-MSC Advantages: Levels of Immunomodulator Secretion

    i - MSC Advantages: Levels of Immunomodulator Secretion 27 i - MSCs secrete higher levels of many immunomodulatory proteins Example: MMP - 1 = 6,500 pg/ml MMP - 1 = 330 pg/ml Example: VEGF - A = 10,800 pg/ml VEGF - A = 3,000 pg/ml Example: MMP - 1 = 6,500 pg/ml MMP - 1 = 330 pg/ml *MMP - 1: member o

  28. Slide 28: NoveCite i-MSC Mouse Study

    NoveCite i - MSC Mouse Study

  29. Slide 29: i-MSCs vs. MSCs: Therapeutic Effect in MS Mouse Model

    i - MSCs vs. MSCs: Therapeutic Effect in MS Mouse Model 29 Novellus i - MSCs improve clinical score in an EAE mouse model – Tail - vein injection of 20 million i - MSCs/kg improved score (p<0.001) – Donor - derived MSCs had little/no effect at 20 million and 40 million cells/kg 25 3=Partial hind lim

  30. Slide 30: ARDS Sheep Study

    ARDS Sheep Study

  31. Slide 31: Interim Results in Sheep Model of ARDS

    P/F ratio Pulmonary Lymph Flow Pulmonary Lymph Protein Loss Norepinephrine Requirement Interim Results: Very Strong Beneficial Effect of i - MSCs in Sheep Model of ARDS Improved Oxygenation Reduced Lung Vascular Injury Less systemic shock Overview of findings: In this ovine model of severe ARDS the

  32. Slide 32: Our Solution – NoveCite i-MSCs

    Our Solution – NoveCite i - MSCs Description: • Allogeneic (“off - the - shelf”) i - PSC - derived induced Mesenchymal Stem Cells • High potency i - MSCs – in vitro data showing exponentially higher secretion of immunomodulatory proteins vs. BM - derived MSCs • Footprint - free i - PSCs created usin

  33. Slide 33: Clinical Development Plan

    Clinical Development Plan (estimated as of 12/2020*) Pre - Clinical And Clinical Regulatory Product and CMC 2020 2021 2022 2023 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Pre - Clinical (tox) Studies Chemistry and Manufacturing Control (CMC) Development Phase 3 Clinical Study POC (Sheep) studie

  34. Slide 34: Mino-Wrap

    Mino - Wrap CITI - 101 Minocycline/Rifampin (M/R) Gelatin Film Bioabsorbable Extended Release Antimicrobial Wrap for the Prevention of Breast Tissue Expander Infections

  35. Slide 35: Mino-Wrap: Thesis

    35 NASDAQ: CTXR Mino - Wrap: Thesis The highest risk for TE - related infections occurs at the time of surgery and as long as drains remain in place (about two weeks post - operatively) and there are portals for microbial colonization. Mino - Wrap is a malleable, bioabsorbable, antimicrobial wrap th

  36. Slide 36: Mino-Wrap Development Plan

    36 NASDAQ: CTXR 2019 2020 2021 2022 2023 2024 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Orphan drug request Pre - Clinical And Clinical Regulatory Product and CMC NDA Approval Mino - Wrap Development Plan (estimated as of 12/2020*) Pre - Clinical Studies Chemistry and M

  37. Slide 37: Halo-Lido CITI-002

    Halobetasol /Lidocaine Prescription Strength Topical for Symptomatic Hemorrhoid Treatment Halo - Lido CITI - 002

  38. Slide 38: CITI-002 Halobetasol + Lidocaine

    38 NASDAQ: CTXR CITI - 002 ( halobetasol + lidocaine) Citius’ product candidate would be the first FDA - approved prescription product to treat hemorrhoids in the US OTC Products are the Mainstay for Treatment of Grade I and II • Up to 5% of the U.S. population suffers from hemorrhoids, but there ar

  39. Slide 39: Halo/Lido Development Plan

    39 NASDAQ: CTXR Halo/Lido Development Plan (estimated as of 12/2020*) 2015 2016 2017 2018 2019 2020 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Phase 2a Clinical Study Product and Formulation Development Phase 2b Clinical Study Pre - Clinical Studies FDA Type C meeting IN

  40. Slide 40: Corporate Summary

    40 NASDAQ: CTXR CITIUS Corporate Summary • Addressing attractive diversified multi - billion dollar opportunities – Adjunctive Cancer Care/Infectious Disease and Gastrointestinal Disease • Partnership with Novellus in developing highly promising i - MSC product • Partnership with MD Anderson Cancer

  41. Slide 41: Financial Summary and Current Cap Table

    41 NASDAQ: CTXR Financial Summary (as of 12/31/20) Current Cap Table Sha r es % of Fully Diluted Basic Shares Outstanding 55,576,996 64.7 % Warrants 26,831,988 31.3 % Options 3,390,166 3.9 % Unit Purchase Options 100 , 667 0. 1 % Fully Diluted Shares Outstanding 85,899,817 100% ( 1 ) Beneficial stoc

  42. Slide 42: Contact

    42 NASDAQ: CTXR Citius Pharmaceuticals, Inc. 11 Commerce Drive First Floor Cranford, NJ 07016 www.citiuspharma.com Investor Relations Contact : Andrew Scott – V.P., Corporate Development (908) 967 - 6677 x105 ascott@citiuspharma.com 42

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