Palatin Technologies, Inc. · AMEX:PTN

Palatin Technologies — Investor Presentation (November 2012)

29 slides from Palatin Technologies's investor presentation, November 2012

  1. Slide 1: Palatin Technologies

    Palatin Technologies November 2012 Carl Spana, Ph.D. President & CEO Stephen T. Wills, CPA/MST CFO / COO

  2. Slide 2: Forward-Looking Statement

    Forward-Looking Statement The statements in this presentation that relate to future plans, events or performance are forward-looking statements, which are made pursuant to the safe harbor provisions of Section 21E of the Securities Exchange Act of 1934. Such forward-looking statements involve signif

  3. Slide 3: Company Profile

    Company Profile Palatin Technologies, Inc. (NYSE MKT: PTN) is a biopharmaceutical company developing targeted, receptor-specific peptide therapeutics for the treatment of diseases with significant unmet medical need and commercial potential. 3

  4. Slide 4: Palatin Investment Opportunity

    Palatin Investment Opportunity Well positioned to drive growth through internal pipeline/collaborations  Lead product: bremelanotide (BMT) for the treatment of female sexual dysfunction (FSD) ◦ Unmet medical need with multi-billion dollar market opportunity ◦ Phase 2B clinical trial positive - Top-

  5. Slide 5: Pipeline

    Pipeline Program Indication Preclinical Phase I Phase II Phase III Bremelanotide Female Sexual Dysfunction Melanocortin MCR-4 Agonist Receptor (partnered with Obesity and Diabetes (MCR) AstraZeneca) Programs Next generation Female Sexual Dysfunction peptide and Erectile Dysfunction PL-3994: Natriure

  6. Slide 6: Female Sexual Dysfunction Program

    Female Sexual Dysfunction Program —

  7. Slide 7: Female Sexual Dysfunction Overview

    Female Sexual Dysfunction Overview  Female Sexual Dysfunction (FSD) is defined as persistent or recurring problems during one or more of the stages of sexual response with associated distress  FSD is prevalent in U.S. adult women ◦ ~43% experiencing some symptoms of FSD ◦ ~23% experiencing associa

  8. Slide 8: FSD: Significant Untapped Market Opportunity

    FSD: Significant Untapped Market Opportunity  No FDA approved treatments available  50 million pre-menopausal women in US o 22% reported a sexual problem o 9% were distressed by their sexual problems • One-third sought formal care  Market size – U.S. o Potential presenting pre-menopausal women ~1

  9. Slide 9: Bremelanotide Profile

    Bremelanotide Profile  First-in-class melanocortin receptor 4 agonist for FSD  On-demand use with rapid onset of activity and well-tolerated  Novel mechanism of action activating endogenous pathways involved in sexual arousal response  Evaluated in 30 clinical studies showing efficacy in both FS

  10. Slide 10: BMT Subcutaneous Development

    BMT Subcutaneous Development  Demonstrated optimal pharmacokinetics ◦ Subcutaneous on-demand formulation: less variation in patient exposure ◦ Good therapeutic dosing window to avoid potential AE’s (GI and BP effects) associated with over-exposure  Completed and submitted preclinical toxicology to

  11. Slide 11: Female Sexual Response Cycle

    Female Sexual Response Cycle Key points for drug intervention are the sites of bremelanotide action 11

  12. Slide 12: Bremelanotide FSD Clinical Data

    Bremelanotide FSD Clinical Data  Studies of sexual function in female rodent and primate models demonstrated pronounced effects on perceptive and appetitive sexual behaviors  Multiple Phase 2 efficacy studies ◦ Double-blind, placebo-controlled ◦ In-clinic dosing and “at-home” use ◦ SC or IN dosing

  13. Slide 13: BMT Phase 2B FSD Clinical Trial

    BMT Phase 2B FSD Clinical Trial  Dose ranging 16 week at-home placebo-controlled study ◦ Subcutaneous dosing: placebo; 0.75 mg BMT; 1.25 mg BMT and 1.75 mg BMT ◦ Target enrollment: 400 patients  Used FDA accepted and validated endpoints ◦ Increase in Satisfying Sexual Events (SSE’s) ◦ As measured

  14. Slide 14: Phase 2B Clinical Data

    Phase 2B Clinical Data  Analysis of the primary and key secondary endpoints of 327 pre-menopausal patients shows clinically meaningful and statistically significant effects for BMT vs. placebo  Primary endpoint ◦ Improvement in the number of satisfying sexual events BMT vs. Placebo (p=0.018) ‒ BMT

  15. Slide 15: Phase 2B Clinical Data

    Phase 2B Clinical Data  395 premenopausal FSD patients were randomized to receive drug or placebo  26 patients met the predefined BP withdrawal criteria and were evenly distributed among placebo and active arms of the study  12 patients withdrew for AE’s (2 on placebo), predominately emesis, naus

  16. Slide 16: BMT FSD Next Steps

    BMT FSD Next Steps  Complete data analysis by 4Q12  End-of-Phase 2 meeting with FDA 1Q13  Full data presentation at scientific conferences 1Q13  Corporate partnership  Start of Phase 3 program targeted for 4Q13 16

  17. Slide 17: Summary of BMT FSD Program

    Summary of BMT FSD Program  Multiple Phase 2 studies establish proof-of-concept in FSD  Phase 2B study met all key objectives and supports transition to Phase 3 development  Subcutaneous formulation has consistent pharmacokinetics and is well-tolerated  BMT continues to demonstrate a positive pa

  18. Slide 18: Melanocortin Receptor Agonist Obesity & Diabetes

    Melanocortin Receptor 4 Agonist Obesity & Diabetes

  19. Slide 19: AstraZeneca Obesity Collaboration

    AstraZeneca Obesity Collaboration  Exclusive global licensing and research collaboration ◦ $10M upfront and $12M milestones received ◦ $145M in additional milestones ◦ Royalties upon commercialization  Clinical proof-of-concept studies for MCR-4 mechanism have been completed ◦ Primary objectives m

  20. Slide 20: Melanocortins and Obesity Overview

    Melanocortins and Obesity Overview  MCR-4 neurons located in the hypothalamus play a key role in coordinating central, peripheral and behavioral signals of energy balance  MCR-4 neurons are activated by a variety of appetite suppressing signals resulting in decreased hunger and increased energy ex

  21. Slide 21: Natriuretic Peptide Receptor Program

    Natriuretic Peptide Receptor Program —_

  22. Slide 22: Acute Severe Asthma

    Acute Severe Asthma  Asthma episode in which symptoms do not adequately respond to current therapies  Patients often require emergency room (ER) treatment  ER Standard of Care requires several hours and patients remain at risk  Recent FDA guidance has questioned the safety of beta-agonist monoth

  23. Slide 23: PL-3994 Market Opportunity

    PL-3994 Market Opportunity Administration Indication Stage Market Potential Subcutaneous Acute Severe Asthma ER Phase 2 >$500M* Acute Severe Asthma ER Rescue Nebulized Preclinical >$1B Medication PRN Broader and Chronic Inhalation/DPI Planned >$3B COPD/Asthma** *Individual treatment cost $1,000 **Cr

  24. Slide 24: PL-3994 Overview

    PL-3994 Overview  Guanylate Cyclase-A (GC-A) activators have clinical precedent as effective bronchodilators in asthmatics ◦ PL-3994: novel direct acting GC-A activator  NPR-A agonism relaxes smooth muscle in airways ◦ Effect maintained under conditions of 2 overload  Half-life of 3 hours in man

  25. Slide 25: PL-3994 in Asthma Disease Models

    PL-3994 in Asthma Disease Models 100 Isolated guinea-pig trachea 15 Intra-tracheal instillation of PL-3994;  in pulmonary inflation effect on inflation pressure in guinea pigs pressure (cmH 2O) 80 % Inhibition of contraction PL3994 PL5731 10 60 Vehicle 40 5 20 0 control 100 g/kg 10 g/kg 1 g/kg 0

  26. Slide 26: PL-3994 Program

    PL-3994 Program  Subcutaneous formulation ◦ Phase 2 proof-of-principle study in stable asthmatics ◦ Placebo-controlled dose escalation crossover study design ◦ Objective is to determine if patients can have a clinically meaningful increase in pulmonary function (FEV1)  Nebulized formulation activi

  27. Slide 27: Milestones

    Milestones  Bremelanotide Phase 2B study in FSD patients ◦ Complete patient enrollment 1Q12 ◦ Positive Top-line data released 4Q12 ◦ EOP2 meeting targeted 1Q13 ◦ Corporate collaboration 2013  AstraZeneca MCR development obesity/diabetes program ◦ Clinical candidate selection 4Q12 ◦ Phase 1 clini

  28. Slide 28: Financial Snapshot

    Financial Snapshot  Ticker Symbol NYSE MKT: PTN  Shares Outstanding – September 30, 2012 ◦ Common 38.9M ◦ Fully Diluted 133.6M  Market Capitalization – September 30, 2012 $27.0M  Cash and Cash Equivalents Balance – September 30, 2012 $33.5M 28

  29. Slide 29: Thank You

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