Pfizer, Inc. · NYSE:PFE

Pfizer — 28th Annual J.P. Morgan Healthcare Conference (January 2010)

20 slides from Pfizer's conference presentation, Jan 12, 2010

  1. Slide 1: Delivering High Impact Medicines That Transform Patients Lives

    Delivering High Impact Medicines That Transform Patients Lives Martin Mackay, President PharmaTherapeutics JP Morgan January 2010

  2. Slide 2: Forward-Looking Statements

    Forward-Looking Statements  This presentation will include forward-looking statements. Actual results could differ materially from those projected in the forward-looking statements. The factors that could cause actual results to differ are discussed in Pfizer’s 2008 Annual Report on Form 10-K and i

  3. Slide 3: Operating Model

    Operating Model Nine Diverse Business Units Supported by Two Research Organizations PharmaTherapeutics BioPharmaceutical Businesses Research & Development Primary Specialty Established Emerging Oncology Care Care Products Markets BioTherapeutics Diversified Businesses Research & Development Consumer

  4. Slide 4: The New R&D Organization

    The New R&D Organization  R&D biomedical presence in US, Europe, Canada and China  5 Major sites Footprint  9 Specialized units  Reduced site footprint by 35%  Closed 6 R&D sites/consolidated 4 R&D sites  Invest to Win Projects increased 50% to 70% Portfolio  Research portfolio prioritization

  5. Slide 5: Innovative Therapies In Key Areas Of Unmet Medical Need

    Innovative Therapies In Key Areas Of Unmet Medical Need Neuroscience Pain/Inflammation Oncology Metabolic Disorders Our Focus Is on High Priority Disease Areas and Enhanced Biologics Capabilities Vaccines Infectious Diseases Biotherapeutics 5

  6. Slide 6: Early Stage: Human Genetics & Cell Biology Are Revolutionizing Target Selection

    Early Stage: Human Genetics & Cell Biology Are Revolutionizing Target Selection Molecular Profiling Stem Cells Systems Biology Target Selection Human Genetics Bioimaging 6

  7. Slide 7: NaV1.7: Exciting New Pain Target

    NaV1.7: Exciting New Pain Target  NaV 1.7 channel modulator will reduce pain by limiting Hypothesis the frequency of firing of pain sensing nerves  Sodium channels responsible for detection and conduction of pain  Human clinical genetic NaV 1.7 mutations have extreme pain phenotypes CIP Erythrome

  8. Slide 8: Today's Phase 3 Portfolio

    Today’s Phase 3 Portfolio  apixaban – VTE Prevention  CP-690,550 – Rheumatoid Arthritis  Thelin – Pulmonary Hypertension  Zithromax/chloro – Malaria  Dimebon – Alzheimer’s Disease  tanezumab – OA Pain  figitumumab – Lung Cancer  bosutinib – Chronic Myelogenous Leukemia NMEs  bapineuzumab –

  9. Slide 9: Select Late Stage Candidates

    Select Late Stage Candidates  Prevnar 13 for Adults (Vaccine) Vaccine  Tanezumab (NGF Antibody) Pain  CP-690550 (JAK3 Inhibitor) Rheumatoid Arthritis  Dimebon (MPTP Modulator) Alzheimer’s Disease  Bapineuzumab (IV Pass Mono Antibody) Alzheimer’s Disease  PF-2341066 (c-Met/ALK Inhibitor) NSCLC

  10. Slide 10: Prevnar 13: Expanding The Opportunity

    ™: Expanding The Opportunity Prevnar 13™ Infant Adult  Provide Broadest Coverage  Provide First and Only Available for the Global Conjugate Vaccine That Protection of Children Offers Adults, >50, an Opportunity Against Pneumococcal Opportunity to Prevent Disease Pneumococcal Pneumonia for the Rest

  11. Slide 11: Pain Therapeutics: Broad Mechanistic Approach, Multiple Modalities

    Pain Therapeutics: Broad Mechanistic Approach, Multiple Modalities 1 Peripheral Sensitization  Celebrex (gout, Ph3b)  Tanezumab (Ph3)  CGRP antibody (migraine, Ph1)  Peripheral u opioid agonist (LD) 4 2 Pain Transduction & Conduction  Nav1.7 blocker (LD)  Nav1.8 blocker (Ph1, SDS)  TrpV1 bloc

  12. Slide 12: Tanezumab: Pain Responder Rates

    Tanezumab: Pain Responder Rates Osteoarthritis 100% 90% *** 80% *** Placebo (n=73) *** Percent of Patients 70% * *** tanezumab 10 g/kg (n=73) 60% * tanezumab 25 g/kg (n=75) 50% tanezumab 50 g/kg (n=72) 40% 30% tanezumab 100 g/kg (n=74) 20% tanezumab 200 g/kg (n=72) 10% 0% 30% Responders 50% Res

  13. Slide 13: CP-690,550: RA Phase 2 Program Conclusions

    CP-690,550: RA Phase 2 Program Conclusions  4/4 studies achieved statistical significance on the primary endpoint (ACR20 Response)  Extensive Phase 2 RA Program enrolled >1,000 patients and explored a CP-690,550 dose range of 1 to 30 mg BID  CP-690,550 dosed  3 mg BID was generally efficacious,

  14. Slide 14: Multiple Approaches To Treat AD Spanning Small Molecules, Biologics, And Vaccines

    Multiple Approaches To Treat AD Spanning Small Molecules, Biologics, And Vaccines 4 Amyloid Pathway 7 5 1 Anti-A antibody (Ph 3, Ph 2, PC) 2 Anti-A vaccine (Ph 2) 1 2 3 RAGE antagonist (Ph 2) 3 4 -Secretase inhibitor (Ph 1, LD) 5 BACE inhibitor (LD) 1 2 Tau Pathway 6 6 Tau vaccine (LD) 1 2 Modula

  15. Slide 15: Dimebon: Affects Cognition In Mild-To-Moderate AD

    Dimebon: Affects Cognition In Mild-To-Moderate AD Treatment p = 0.0077 p < 0.0001 p < 0.0001 p < 0.0001 Effect 2.0 4.0 5.9 6.9 –3.0 Mean Change From Baseline –2.0 Clinical –1.0 Improvement Score ADS-cog 0.0 1.0 2.0 3.0 4.0 5.0 Dimebon (n = 89) Clinical 6.0 Deterioration Placebo (n = 94) Baseline 12

  16. Slide 16: Bapineuzumab: Alzheimer's Disease

    Bapineuzumab: Alzheimer’s Disease  Four Studies in Over 4,000 Patients Worldwide  Patients Are Stratified by ApoE4 Carriers vs. Non-Carriers  Co-Primary Efficacy Endpoints – Validated Cognitive and Functional Scales  Phase 2 Data Presented at ICAD – July 2008  Safety and Efficacy Findings Suppo

  17. Slide 17: PF-2341066: NSCLC

    PF-2341066: NSCLC  Novel c-Met/ALK Inhibitor is the First Agent in Clinical Development to Selectively Target Sub-group of NSCLC Patients  ASCO 2009 – Presented new study results from an expansion cohort of a Phase 1 study in patients with NSCLC carrying the ALK (anaplastic lymphoma kinases) fusio

  18. Slide 18: PF-2341066 (cMet Alk) Pre-Treatment (FLT-PET)

    PF-2341066 (cMet Alk) 43 yr old Male with Stage IV NSCLC positive for EML4-ALK Pre-Treatment (FLT-PET) After 1 Cycle PF-2341066 18

  19. Slide 19: Working Together To Progress Assets, Programs And Technologies

    Working Together To Progress Assets, Programs And Technologies Areas of Interest Types of Relationships Alzheimer’s Biotherapeutics Licensing Disease Vaccines Co-develop/Co-promote Diabetes Biomarkers Alliances Inflammation & Regenerative Medicine Venture Investments Immunology Consumer Healthcare M

  20. Slide 20: Drug Discovery Heroes Heart of What We Do

    Drug Discovery Heroes Vaccine Expertise Heart of What We Do Neuroscience Expertise 20

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