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2009 JP Morgan Conference


                Martin Mackay
              President, PGRD
              January 13, 2009
Forward-Looking Statements


  Discussions at this meeting 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 2007 Annual Report on Form 10-K and in our
  reports on Form 10-Q and Form 8-K

  These reports are available on our website at
  www.pfizer.com in the quot;Investors—SEC Filingsquot; section
Martin Mackay
  President, PGRD
PGRD’s Five Strategic Elements


1 Aggressively Deliver the Phase 2 and
   Phase 3 Portfolio

2 Prioritize Our Portfolio to Deliver the
   Most Value

3 Become a Top-Tier Biotherapeutics
   Company

4 Dramatically Raise the Bar
   on Productivity

5 Pursue the Best External Science
2008 Achievements

                                                   Global Submissions
            Global Approvals
 Fesoterodine Overactive Bladder (US)     Fablyn Osteoporosis Treatment (Europe)
 Maraviroc HIV Treatment in               Lyrica Post Herpetic Neuralgia (Japan)
 Experienced Patients (Japan)
                                          Xalacom Glaucoma (Japan)
 Macugen Age-Related Macular
                                          Maraviroc HIV Treatment Experienced
 Degeneration (Japan)
                                          Patients (Japan)
 Rifabutin Bacterial Infections (Japan)
                                          Maraviroc HIV Treatment Naïve Patients
 Sutent Gastrointestinal Stromal Tumor    (US)
 (Japan)
                                          Lyrica Oral Solution (Europe)
 Champix Smoking Cessation (Japan)
                                          Revatio IV Formulation (US and Europe)
 Genotropin Short Stature/Growth
                                          Geodon Bipolar Mania Maintenance Adult
 Problems (Japan)
                                          (US)
 Zithromax SR Peds Bacterial Infections
                                          Geodon Peds (US and Europe)
 (US)
                                          Norvasc 10mg dosing (Japan)
 Sutent Renal Cell Cancer (Japan)
                                          Lyrica Fibromyalgia (Europe)
 Revatio Pulmonary Arterial
 Hypertension (Japan)                     Zithromax SR Bacterial Infections
                                          (Japan)
2008 Achievements

                                                Business Development
         Advanced to Phase 3
 Dimebon Alzheimer’s Dementia             Auxilium Xiaflex for Dupuytren’s
                                          contracture and Peyronie’s Disease
 Tanezumab OA Signs and Symptoms
                                          Sigma-Tau Eurartesim for malaria
 CP-751871 Non-Small Cell Lung Cancer
                                          Medivation Dimebon for Alzheimer’s and
 Axitinib Pancreatic Cancer
                                          Huntington’s Disease
 Axitinib 2nd Line Renal Cell Carcinoma
                                          UCB Cyclofluidic
 (US and Japan)
                                          Eyecyte New Paradigm of Drug
 Lyrica Restless Leg Syndrome
                                          Development
 Xalatan Peds Glaucoma
                                          UPENN Collaboration with UPENN
 Sutent Prostate Cancer
                                          School of Medicine
 Sutent Hepatocellular Cancer
                                          UCSF Alliance to Advance Broad Range
 Apixaban VTE Treatment                   of Research
 Sutent Colorectal Cancer                 Five Prime Therapeutics Oncology and
 Gabapentin Peds Epilepsy                 Diabetes Collaboration
 Geodon Adj use in Bipolar Depression     AVANT/Celldex CDX-110 Glioblastoma
                                          Multiforme
 Maraviroc Peds HIV
                                          Encysive Acquisition
             Early Portfolio              Serenix Acquisition
                                          Scil Novel Cartilage Growth Factor
 10 POCs, 19 FIPs, 26 FIHs
Innovating Our Model with Smaller,
More Accountable Business Units

 Primary      Specialty                        Established       Emerging    Animal
                             Oncology
  Care          Care                            Products          Markets    Health




                                            Business Units
      Research and
   Biotherapeutics &
                             Late-Stage                       Sales &
  Bioinnovation Center                         Medical
                            Development                      Marketing


                                        Manufacturing
                                                                            Customer
                                                                            Focused
                            Partner Lines



                         Enabling Functions
Advancing Compounds in the Pipeline

                      Pipeline as of Sept 30, 2008



Over 300                                                         Total
            Phase 1       Phase 2       Phase 3        In Reg.
Discovery     50            38            25              1
                                                                  114
Projects



                      Goals (Announced March 2008)
                 15–20 Phase 3 starts in 2008 – 2009
                 24–28 Programs in Phase 3 by end of 2009
                 15–20 Submissions 2010 – 2012



                  On-Track to Meet These Goals
Recent Disease Area Decisions

               Disease Area Focus                                                        Disease Area Exits*

         Alzheimer’s Disease                                                       Anemia
         Diabetes                                                                  Atherosclerosis/Hyperlipidemia
         Inflammation/Immunology                                                   Bone Health/Frailty
         Oncology                                                                  Gastrointestinal
         Pain                                                                      Heart Failure
         Psychosis                                                                 Liver Fibrosis
         Asthma/COPD                                                               Muscle
         Genitourinary                                                             Obesity
         Infectious Disease                                                        Osteoarthritis
         Ophthalmology                                                             Peripheral Arterial Disease

*Does not affect our portfolio of marketed products, the development of compounds in Phase 3 or any launches planned in the next three years
Biotherapeutics and Bioinnovation Center

Federation of Technology-aligned Research Units and Biologic-generating Companies

                                                    San Francisco
                                                          fabrus

                                                        UCSF/QB3
                                               Ambryx                FivePrime

                                                         Rinat
                                                        Antibodies
                                   Scripps                                       MGH



                                         CovX                            RTC
                           Wint-
             San Diego                                                                        Boston
                                                         BBC                            RGo
                           herix                                         RNAi
                                         Peptides



                                   Isogenica                                     Bend
                                                         PRM*
                                                        Stem Cells
     Research Unit
                                                        Novocell
     Collaborations
     Incubator
     Portfolio Company                                   EyeCyte

                                                        Europe
*Collaboration with PGRD
Biotherapeutics in the Pipeline


    Research            Development                     Marketed


      72                    17                               5
                                                    $1.2B Est.
                                                2008 Revenues
      Diverse Portfolio

             9 TAs                    (interferon beta-1a)
                                                             (dalteparin sodium injection)

         6 Modalities
           53 MAbs
          9 Vaccines
Today’s Phase 3 Portfolio

              axitinib – Pancreatic Cancer        esreboxetine – Fibromyalgia
              apixaban – VTE Prevention           Zithromax/chloro – Malaria
              Thelin – Pulmonary Hypertension     Dalbavancin – Skin & Skin
   NMEs                                           Structure Infections
              Dimebon – Alzheimer’s Disease
                                                  tanezumab –OA Pain
              CP-751871 – Lung Cancer
                                                  Xiaflex – Dupuytren’s
              PD-332334 – GAD
                                                  contracture




                                              /
   New        apixaban –
              Atrial Fibrillation
Indications
              apixaban – VTE Treatment
              axitinib – Renal Cell Cancer
Rebuilding the Phase 3 Portfolio

                 Number of Phase 3 Programs

                                                     24–28
                                      26



                         16


           8




       Jan '07      Mar '08       Dec '08          Dec '09
                  Analyst Day     Actual          Projected

                  NMEs          New Indications
Select Late Stage Candidates



    Tanezumab (NGF Antibody)                Pain

    CP-690550 (JAK3 Inhibitor)              Rheumatoid Arthritis

    Dimebon (MPTP Modulator)                Alzheimer’s Disease

    CP-751871 (IGF1R Antibody)              Lung Cancer

    Sutent (Multiple Tyrosine Kinase Inh)   Breast Cancer
Tanezumab: Overview


  Acquired as part of Rinat deal
                                                                                 Heavy
     Humanized, IgG2 MAb                                                         Chain
     High specificity and affinity for NGF

  Fast to market strategy with Osteoarthritis (OA)                                      NGF

  Clinical efficacy demonstrated in OA
     5 minute I.V. administration
     Low projected dose < 10 mg once every 8 wks
                                                                                Light
     Phase 3 program: Nov 2008                                                  Chain

  Additional Phase 2 studies
     Completed; Chronic low back pain; Results at the 2009 American Pain Society
     Meeting
     Ongoing: Post-herpetic neuralgia, interstitial cystitis, Japan OA I.V. bridging;
     S.C. PK
     Initiating: Prostatitis; metastatic bone pain, endometriosis
Tanezumab: Walking Knee Pain
(Mean Change ± Standard Error)

                                                       Week
                                        1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
                                                                                 Mean Change from Baseline
                                   0
                                                                                   Over Weeks 1–16 (SE)
  Change in VAS from Baseline




                                 -10                                                 Placebo     -15.5 (2.6)
                                                                                     Tanezumab   -32.1 (2.5)*
      LS Mean (SE), mm




                                                                                     10 µg/kg
                                 -20
                                                                                     Tanezumab   -36.0 (2.5)*
                                                                                     25 µg/kg
                                 -30
                                                                                     Tanezumab   -31.0 (2.6)*
                                                                                     50 µg/kg
                                 -40
                                                                                     Tanezumab   -42.5 (2.5)*
                                                                                     100 µg/kg
                                 -50
                                                                                     Tanezumab   -45.2 (2.6)*
                                                                                     200 µg/kg
                                 -60

                                 Study Drug          Study Drug
                                Administration      Administration
*P<.0001 vs. placebo
CP-690550 (JAK-3): Overview

  Small molecule discovered in    Evidence of efficacy in multiple
  Groton Labs                     human diseases of
                                  immunological dysregulation
  Key Milestones                     RA, kidney allograft rejection,
                                     and psoriasis, all have continuing
    FIH – March 2002
                                     Phase 2 programs
    POM – June 2004
                                     Phase 2 program also
    FIP – Dec 2004                   undertaken in IBD
    POC – July 2006
    Rheumatoid Arthritis (RA)
    chosen as lead indication
    Scheduled for Phase 3 start
    March 2009
CP-690550 (JAK-3):
Positive Primary Efficacy Results
                         Phase 2 RA Studies



          12 Weeks Plus Background MTX in     6 Weeks Monotherapy in Patients
          Patients with Inadequate Response     Who Had Failed MTX or a Tnfi
               to a Stable Dose of MTX
Dimebon: Overview


   Co-development with Medivation, Inc.
   Dimebon primary mechanism of action
     Enhances mitochondrial function
     Other pathways may also contribute
  In development for AD (Phase 3) and
  Huntington’s disease (HD, Phase 2)
     Clinical efficacy demonstrated across 5
     clinical endpoints
     Improvement in cognitive endpoint in
     Phase 2 HD
  Phase 3 Studies
     Ongoing: 6 month monotherapy in
     mild-moderate AD (CONNECTION)
     Several others initiating in 2009
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
                                                                                                       Deterioration
                             6.0         Placebo (n = 94)

                                   Baseline           12           26           39           52
                                                                        Week
        * Similar results were seen with the MMSE over 1 year
        Doody RS, et al. Lancet. 2008;372:207-215.
CP-751871 (figitumumab): Overview

  Anti-IGF-1R mAb discovered in Groton Labs

  Fully human, IgG2 MAb

  First-in-class opportunity in highly
  competitive arena
     First selective anti-IGF mAb to enter human trials
     First to generate published Phase 2 data
     First to start formal Ph3 trials in mid-2008

  Over 1000 patients have participated in CP-751
  clinical trials
     Very well tolerated with no dose-limiting toxicity
     seen to date
     Combinable with a wide variety of currently used
     standard of care agents
     Promising signs of clinical activity in lung cancer
     and sarcoma
     On-going Ph3 registration program in lung cancer
     Ph2 investigations of risk/benefit on-going in breast,
     colorectal, prostate and sarcoma


 IGF-1R – Receptor on Cell Surface Triggering Key Pathways That Drive Cancer Cell Survival
CP-751871:
Plus Chemotherapy in 1st Line NSCLC
Responses in Bulky Squamous Tumors

                   US           Spain           Italy
           October 2005      August 2007    November 2007




          February 2006      October 2007     April 2008




Ref: Karp et al, ASCO 2008
Sutent: Potential New Indications
Expected to Drive Value



                                    Colorectal




                     es
                   nu
                 ve                 Non-Small Cell Lung
                Re

                                    Hepatocellular
                                    Carcinoma

                                    Breast


                                    Renal Cell Carcinoma &
                                    Gastrointestinal Stromal
                                    Tumor


                Time
Sutent: Breast Cancer


  Clinical anti-tumor activity in breast cancer
    Demonstrated in Phase 2, single-agent study in heavily pre-
    treated, advanced disease (ASCO, 2005)
    Preclinical and clinical rationale to combine and improve
    treatment with chemotherapy
     – Example: Phase 1 combination docetaxel + SU (n = 22)
     – Objective Response Rate 72% (SABC, 2007)
    Multiple Phase 1/2 single-agent and combination studies with
    docetaxel, paclitaxel, capecitabine, trastuzumab
     –   HER-2 (-) breast cancer
     –   HER-2 (+) breast cancer
     –   Triple-negative breast cancer
     –   Locally-recurrent breast cancer
Commitments



     On Track to Meet our March 5, 2008 Commitments


         15–20 Phase 3 starts by end of 2009

         24–28 Phase 3 programs by end of 2009

         15–20 Submissions by 2010–2012
Working Together to Progress Assets,
Programs and Technologies

              Areas of Interest            Types of Relationships
  Alzheimer’s         Infectious Disease   Licensing
  Disease
                      Ophthalmology        Co-develop/Co-promote
  Diabetes
                      Smoking Cessation    Alliances
  Inflammation &
                      Thrombosis           Venture Investments
  Immunology
                      Biotherapeutics      M&A
  Oncology
                      Vaccines             Out Licensing
  Pain
                      Science &            Academic
  Psychosis
                      Technologies
  Asthma/COPD
                      Regenerative
  Genitourinary       Medicine

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Pfizer at the 27th Annual J.P. Morgan Healthcare Conference

  • 1. 2009 JP Morgan Conference Martin Mackay President, PGRD January 13, 2009
  • 2. Forward-Looking Statements Discussions at this meeting 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 2007 Annual Report on Form 10-K and in our reports on Form 10-Q and Form 8-K These reports are available on our website at www.pfizer.com in the quot;Investors—SEC Filingsquot; section
  • 3. Martin Mackay President, PGRD
  • 4. PGRD’s Five Strategic Elements 1 Aggressively Deliver the Phase 2 and Phase 3 Portfolio 2 Prioritize Our Portfolio to Deliver the Most Value 3 Become a Top-Tier Biotherapeutics Company 4 Dramatically Raise the Bar on Productivity 5 Pursue the Best External Science
  • 5. 2008 Achievements Global Submissions Global Approvals Fesoterodine Overactive Bladder (US) Fablyn Osteoporosis Treatment (Europe) Maraviroc HIV Treatment in Lyrica Post Herpetic Neuralgia (Japan) Experienced Patients (Japan) Xalacom Glaucoma (Japan) Macugen Age-Related Macular Maraviroc HIV Treatment Experienced Degeneration (Japan) Patients (Japan) Rifabutin Bacterial Infections (Japan) Maraviroc HIV Treatment Naïve Patients Sutent Gastrointestinal Stromal Tumor (US) (Japan) Lyrica Oral Solution (Europe) Champix Smoking Cessation (Japan) Revatio IV Formulation (US and Europe) Genotropin Short Stature/Growth Geodon Bipolar Mania Maintenance Adult Problems (Japan) (US) Zithromax SR Peds Bacterial Infections Geodon Peds (US and Europe) (US) Norvasc 10mg dosing (Japan) Sutent Renal Cell Cancer (Japan) Lyrica Fibromyalgia (Europe) Revatio Pulmonary Arterial Hypertension (Japan) Zithromax SR Bacterial Infections (Japan)
  • 6. 2008 Achievements Business Development Advanced to Phase 3 Dimebon Alzheimer’s Dementia Auxilium Xiaflex for Dupuytren’s contracture and Peyronie’s Disease Tanezumab OA Signs and Symptoms Sigma-Tau Eurartesim for malaria CP-751871 Non-Small Cell Lung Cancer Medivation Dimebon for Alzheimer’s and Axitinib Pancreatic Cancer Huntington’s Disease Axitinib 2nd Line Renal Cell Carcinoma UCB Cyclofluidic (US and Japan) Eyecyte New Paradigm of Drug Lyrica Restless Leg Syndrome Development Xalatan Peds Glaucoma UPENN Collaboration with UPENN Sutent Prostate Cancer School of Medicine Sutent Hepatocellular Cancer UCSF Alliance to Advance Broad Range Apixaban VTE Treatment of Research Sutent Colorectal Cancer Five Prime Therapeutics Oncology and Gabapentin Peds Epilepsy Diabetes Collaboration Geodon Adj use in Bipolar Depression AVANT/Celldex CDX-110 Glioblastoma Multiforme Maraviroc Peds HIV Encysive Acquisition Early Portfolio Serenix Acquisition Scil Novel Cartilage Growth Factor 10 POCs, 19 FIPs, 26 FIHs
  • 7. Innovating Our Model with Smaller, More Accountable Business Units Primary Specialty Established Emerging Animal Oncology Care Care Products Markets Health Business Units Research and Biotherapeutics & Late-Stage Sales & Bioinnovation Center Medical Development Marketing Manufacturing Customer Focused Partner Lines Enabling Functions
  • 8. Advancing Compounds in the Pipeline Pipeline as of Sept 30, 2008 Over 300 Total Phase 1 Phase 2 Phase 3 In Reg. Discovery 50 38 25 1 114 Projects Goals (Announced March 2008) 15–20 Phase 3 starts in 2008 – 2009 24–28 Programs in Phase 3 by end of 2009 15–20 Submissions 2010 – 2012 On-Track to Meet These Goals
  • 9. Recent Disease Area Decisions Disease Area Focus Disease Area Exits* Alzheimer’s Disease Anemia Diabetes Atherosclerosis/Hyperlipidemia Inflammation/Immunology Bone Health/Frailty Oncology Gastrointestinal Pain Heart Failure Psychosis Liver Fibrosis Asthma/COPD Muscle Genitourinary Obesity Infectious Disease Osteoarthritis Ophthalmology Peripheral Arterial Disease *Does not affect our portfolio of marketed products, the development of compounds in Phase 3 or any launches planned in the next three years
  • 10. Biotherapeutics and Bioinnovation Center Federation of Technology-aligned Research Units and Biologic-generating Companies San Francisco fabrus UCSF/QB3 Ambryx FivePrime Rinat Antibodies Scripps MGH CovX RTC Wint- San Diego Boston BBC RGo herix RNAi Peptides Isogenica Bend PRM* Stem Cells Research Unit Novocell Collaborations Incubator Portfolio Company EyeCyte Europe *Collaboration with PGRD
  • 11. Biotherapeutics in the Pipeline Research Development Marketed 72 17 5 $1.2B Est. 2008 Revenues Diverse Portfolio 9 TAs (interferon beta-1a) (dalteparin sodium injection) 6 Modalities 53 MAbs 9 Vaccines
  • 12. Today’s Phase 3 Portfolio axitinib – Pancreatic Cancer esreboxetine – Fibromyalgia apixaban – VTE Prevention Zithromax/chloro – Malaria Thelin – Pulmonary Hypertension Dalbavancin – Skin & Skin NMEs Structure Infections Dimebon – Alzheimer’s Disease tanezumab –OA Pain CP-751871 – Lung Cancer Xiaflex – Dupuytren’s PD-332334 – GAD contracture / New apixaban – Atrial Fibrillation Indications apixaban – VTE Treatment axitinib – Renal Cell Cancer
  • 13. Rebuilding the Phase 3 Portfolio Number of Phase 3 Programs 24–28 26 16 8 Jan '07 Mar '08 Dec '08 Dec '09 Analyst Day Actual Projected NMEs New Indications
  • 14. Select Late Stage Candidates Tanezumab (NGF Antibody) Pain CP-690550 (JAK3 Inhibitor) Rheumatoid Arthritis Dimebon (MPTP Modulator) Alzheimer’s Disease CP-751871 (IGF1R Antibody) Lung Cancer Sutent (Multiple Tyrosine Kinase Inh) Breast Cancer
  • 15. Tanezumab: Overview Acquired as part of Rinat deal Heavy Humanized, IgG2 MAb Chain High specificity and affinity for NGF Fast to market strategy with Osteoarthritis (OA) NGF Clinical efficacy demonstrated in OA 5 minute I.V. administration Low projected dose < 10 mg once every 8 wks Light Phase 3 program: Nov 2008 Chain Additional Phase 2 studies Completed; Chronic low back pain; Results at the 2009 American Pain Society Meeting Ongoing: Post-herpetic neuralgia, interstitial cystitis, Japan OA I.V. bridging; S.C. PK Initiating: Prostatitis; metastatic bone pain, endometriosis
  • 16. Tanezumab: Walking Knee Pain (Mean Change ± Standard Error) Week 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Mean Change from Baseline 0 Over Weeks 1–16 (SE) Change in VAS from Baseline -10 Placebo -15.5 (2.6) Tanezumab -32.1 (2.5)* LS Mean (SE), mm 10 µg/kg -20 Tanezumab -36.0 (2.5)* 25 µg/kg -30 Tanezumab -31.0 (2.6)* 50 µg/kg -40 Tanezumab -42.5 (2.5)* 100 µg/kg -50 Tanezumab -45.2 (2.6)* 200 µg/kg -60 Study Drug Study Drug Administration Administration *P<.0001 vs. placebo
  • 17. CP-690550 (JAK-3): Overview Small molecule discovered in Evidence of efficacy in multiple Groton Labs human diseases of immunological dysregulation Key Milestones RA, kidney allograft rejection, and psoriasis, all have continuing FIH – March 2002 Phase 2 programs POM – June 2004 Phase 2 program also FIP – Dec 2004 undertaken in IBD POC – July 2006 Rheumatoid Arthritis (RA) chosen as lead indication Scheduled for Phase 3 start March 2009
  • 18. CP-690550 (JAK-3): Positive Primary Efficacy Results Phase 2 RA Studies 12 Weeks Plus Background MTX in 6 Weeks Monotherapy in Patients Patients with Inadequate Response Who Had Failed MTX or a Tnfi to a Stable Dose of MTX
  • 19. Dimebon: Overview Co-development with Medivation, Inc. Dimebon primary mechanism of action Enhances mitochondrial function Other pathways may also contribute In development for AD (Phase 3) and Huntington’s disease (HD, Phase 2) Clinical efficacy demonstrated across 5 clinical endpoints Improvement in cognitive endpoint in Phase 2 HD Phase 3 Studies Ongoing: 6 month monotherapy in mild-moderate AD (CONNECTION) Several others initiating in 2009
  • 20. 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 Deterioration 6.0 Placebo (n = 94) Baseline 12 26 39 52 Week * Similar results were seen with the MMSE over 1 year Doody RS, et al. Lancet. 2008;372:207-215.
  • 21. CP-751871 (figitumumab): Overview Anti-IGF-1R mAb discovered in Groton Labs Fully human, IgG2 MAb First-in-class opportunity in highly competitive arena First selective anti-IGF mAb to enter human trials First to generate published Phase 2 data First to start formal Ph3 trials in mid-2008 Over 1000 patients have participated in CP-751 clinical trials Very well tolerated with no dose-limiting toxicity seen to date Combinable with a wide variety of currently used standard of care agents Promising signs of clinical activity in lung cancer and sarcoma On-going Ph3 registration program in lung cancer Ph2 investigations of risk/benefit on-going in breast, colorectal, prostate and sarcoma IGF-1R – Receptor on Cell Surface Triggering Key Pathways That Drive Cancer Cell Survival
  • 22. CP-751871: Plus Chemotherapy in 1st Line NSCLC Responses in Bulky Squamous Tumors US Spain Italy October 2005 August 2007 November 2007 February 2006 October 2007 April 2008 Ref: Karp et al, ASCO 2008
  • 23. Sutent: Potential New Indications Expected to Drive Value Colorectal es nu ve Non-Small Cell Lung Re Hepatocellular Carcinoma Breast Renal Cell Carcinoma & Gastrointestinal Stromal Tumor Time
  • 24. Sutent: Breast Cancer Clinical anti-tumor activity in breast cancer Demonstrated in Phase 2, single-agent study in heavily pre- treated, advanced disease (ASCO, 2005) Preclinical and clinical rationale to combine and improve treatment with chemotherapy – Example: Phase 1 combination docetaxel + SU (n = 22) – Objective Response Rate 72% (SABC, 2007) Multiple Phase 1/2 single-agent and combination studies with docetaxel, paclitaxel, capecitabine, trastuzumab – HER-2 (-) breast cancer – HER-2 (+) breast cancer – Triple-negative breast cancer – Locally-recurrent breast cancer
  • 25. Commitments On Track to Meet our March 5, 2008 Commitments 15–20 Phase 3 starts by end of 2009 24–28 Phase 3 programs by end of 2009 15–20 Submissions by 2010–2012
  • 26. Working Together to Progress Assets, Programs and Technologies Areas of Interest Types of Relationships Alzheimer’s Infectious Disease Licensing Disease Ophthalmology Co-develop/Co-promote Diabetes Smoking Cessation Alliances Inflammation & Thrombosis Venture Investments Immunology Biotherapeutics M&A Oncology Vaccines Out Licensing Pain Science & Academic Psychosis Technologies Asthma/COPD Regenerative Genitourinary Medicine