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Market Research Report

Stakeholder Insight: Inflammatory Bowel Disease - Debate over early aggressive treatment continues

Published by Datamonitor Contact us : +1-860-674-8796
Published 2007/12 Content info 297 pages
Product code DC59589
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Description TOC

Table of Contents

  • ABOUT DATAMONITOR HEALTHCARE
    • About the Immunology and Inflammation pharmaceutical analysis team
  • CHAPTER 1 EXECUTIVE SUMMARY
    • Scope of the analysis
    • Datamonitor insight into the inflammatory bowel disease market
    • Contributing experts
    • Previous and related reports
  • CHAPTER 2 INTRODUCTION AND SCOPE
    • Coverage of the Stakeholder Insight Survey
      • Epidemiology and patient segmentation
      • Diagnosis
      • Treatment options and guidelines
      • Treatment trends
      • Key prescribing influences
      • Brand assessment
  • CHAPTER 3 COUNTRY TREATMENT TREES
    • Introduction to treatment trees
      • US
      • Japan
      • France
      • Germany
      • Italy
      • Spain
      • UK
  • CHAPTER 4 EPIDEMIOLOGY AND PATIENT SEGMENTATION
    • Disease definition
      • Classification of inflammatory bowel disease
        • Crohn' s disease
        • Ulcerative colitis
        • Montreal classification of Crohn' s disease and ulcerative colitis
      • Etiology
        • Genes associated with inflammatory bowel disease influence phenotype
        • Smoking
        • Appendectomy
        • Oral contraceptives
        • Infection with a pathogenic organism
        • Abnormal immune response to gut flora
      • Pathogenesis
        • Crohn' s disease and ulcerative colitis are mediated by Th1 and Th2 lymphocytes, respectively
    • Disease incidence and prevalence
      • Crohn' s disease
      • Ulcerative colitis
      • US
      • Europe
        • France
        • Germany
        • Italy
        • Spain
        • UK
      • Japan
      • Patient segmentation according to disease severity
        • Severity is measured using different disease activity scales
        • Majority of Crohn' s disease and ulcerative colitis patients suffer mild to moderate disease
  • CHAPTER 5 DIAGNOSIS OF INFLAMMATORY BOWEL DISEASE
    • Diagnosis
      • Diagnosis of inflammatory bowel disease combines many avenues of investigation
        • Initial investigation begins with laboratory tests
        • Endoscopy is the most direct way of diagnosing inflammatory bowel disease
        • Radiology is a crucial adjunct to endoscopy
        • Serological markers are not yet used for clinical diagnosis
      • A high diagnosis rate is observed in inflammatory bowel disease
        • Just over 70% of Crohn' s disease patients are diagnosed
        • Physicians report a higher diagnosis rate for ulcerative colitis than Crohn' s disease
      • Complications arising in Crohn' s disease and ulcerative colitis
        • Abscesses, strictures and fistulae are the most commonly physician-reported complications in Crohn' s disease patients
        • Over 25% of Crohn' s disease patients suffer from nutritional deficiencies
        • Bleeding is reported by almost all gastroenterologists in patients with ulcerative colitis
        • Almost half of ulcerative colitis patients experience bleeding complications
      • Association of IBD with immune disorders and co-morbidities
        • Anemia and anxiety and depression are the most commonly associated co-morbidities in inflammatory bowel disease
        • Patients with inflammatory bowel disease also suffer from irritable bowel disease
        • Immune-mediated diseases occur at greater frequency among patients with inflammatory bowel disease
  • CHAPTER 6 TREATMENT OPTIONS AND GUIDELINES
    • Treatment options
      • Non-pharmacological treatment of inflammatory bowel disease
        • Diet
        • Probiotics
      • Pharmacological treatment
        • Antibiotics
        • Anti-diarrheals and anti-spasmodics
        • Topical and oral aminosalicylates
        • Corticosteroids
        • Traditional immunosuppressants
        • Targeted biologics
      • Pharmacological versus non-pharmacological
        • Majority of patients with inflammatory bowel disease are treated pharmacologically
        • There are some patients who do not receive any therapy for inflammatory bowel disease
    • Treatment guidelines
      • Several treatment guidelines exist for the treatment of inflammatory bowel disease
        • Guidelines published by the British Society of Gastroenterology
        • NICE guidelines on the use of infliximab for Crohn' s disease
        • NICE is appraising the use of infliximab for ulcerative colitis
        • American College of Gastroenterology guidelines for Crohn' s disease
        • American College of Gastroenterology guidelines for ulcerative colitis
        • The European Crohn' s and Colitis Organisation has published consensus guidelines for Crohn' s disease
  • CHAPTER 7 TREATMENT TRENDS
    • Changes in therapy
      • Disease severity influences treatment
        • Despite lack of evidence to support efficacy, Crohn' s disease and ulcerative colitis patients receive antibiotics at all levels of severity
        • Anti-spasmodics and anti-diarrheals are used as accompanying therapies for all severities of Crohn' s disease and ulcerative colitis
        • Up to 60% of Crohn' s disease and ulcerative colitis patients receive oral aminosalicylates
        • Topical aminosalicylates are used more for ulcerative colitis than Crohn' s disease
        • Use of corticosteroids increases with disease severity
        • Gradual increase in use of immunosuppressants according to Crohn' s disease severity
        • Immunosuppressants are largely reserved for moderate and severe ulcerative colitis patients
        • Use of biologics in Crohn' s disease occurs in moderate-to-severe disease, but to a limited extent in mild patients
        • Use of biologic increases significantly with severity of ulcerative colitis
      • Monotherapy versus combination therapy
        • Increasing disease severity promotes use of combination therapy
      • First-line therapy
        • Oral 5-ASAs are used first-line for Crohn' s disease
        • Corticosteroids are being prescribed at first-line for Crohn' s disease
        • A combination of oral and topical 5-ASAs is the preferred first-line treatment regimen for ulcerative colitis
        • Almost 45% of Crohn' s disease patients move to a second-line therapy
        • About a third of ulcerative colitis patients progress to treatment with second-line therapy
      • Second-line therapy
        • Immunosuppressants are the most commonly prescribed drug class by gastroenterologists at second-line for Crohn' s disease
        • Biologics are prescribed at second-line for Crohn' s disease
        • Corticosteroids are prescribed at second-line for ulcerative colitis
        • Immunosuppressants are also prescribed at second-line for ulcerative colitis
        • Almost a quarter of Crohn' s disease patients progress from second-line to third-line treatment
        • A fifth of ulcerative colitis patients progress from second-line to third-line treatment
      • Third-line therapy
        • Biologics alone, or in combination with immunosuppressants, are the most commonly prescribed therapies for Crohn' s disease at third-line
        • Like Crohn' s disease, biologics are prescribed most frequently by gastroenterologists for ulcerative colitis
    • Surgery
      • Surgery is more effective for ulcerative colitis than Crohn' s disease
      • Just under a third of Crohn' s disease patients will eventually require surgery
      • Almost half as many patients with ulcerative colitis will eventually require surgery than those with Crohn' s disease
      • Ulcerative colitis patients receive pharmacological therapy for longer than Crohn' s disease patients before requiring surgery
    • "Step-up" versus a "top-down" approach to the treatment of inflammatory bowel disease
      • Current algorithms promote use of a "step-up" approach, but a "top-down" approach is now being suggested
      • Is there scope for a "top-down" approach?
        • Clinical trial data provide evidence showing a "top-down" approach is more effective than "step-up"
        • A "top-down" approach may change the natural history of Crohn' s disease
        • There are a number of advantages and risks associated with a "top-down" treatment approach
        • The SONIC study will assess early use of azathioprine, infliximab or both in combination
      • Only 20% of severe Crohn' s disease patients receive a "top-down" treatment approach
      • The potential for side effects ranks as the leading reason for not using a "top-down" approach in Crohn' s disease
      • Similar percentage of ulcerative colitis and Crohn' s disease patients receive a "top-down" treatment approach
      • The potential for side effects is also the leading reason for not using a "top-down" approach in ulcerative colitis
      • Gastroenterologists also reported that a lack of evidence and experience prevents use of a "top-down" approach
  • CHAPTER 8 PRESCRIBING INFLUENCES
    • Factors influencing physician decision making
      • Symptomatic improvement and healing of the mucosa are the most important factors influencing physician prescribing
      • Efficacy
        • Symptomatic improvement
        • Efficacy in promoting mucosal healing
        • Speed of onset of remission
      • Safety
        • Side-effect profile
      • Dosing
        • Convenient dosing and convenient administration frequency
      • Cost
        • Availability (formulary/reimbursement status)
      • Physician factors
        • Familiarity with product
      • Patient factors
        • Patient compliance
      • Other
        • Prevention of colon cancer
  • CHAPTER 9 BRAND ASSESSMENT
    • Brand map
      • How to interpret a brand map
    • 5-ASAs: Lialda may offer advantages in a class where there is little differentiation
      • Pentasa (mesalazine)
        • Pentasa is an oral, controlled-release formulation that delivers mesalazine from the duodenum to the rectum
        • New dose of Pentasa reduces the number of pills taken per day
        • Gastroenterologists rated Pentasa well on familiarity and availability
      • Lialda/Mezavant (mesalazine)
        • Lialda is an oral sustained-release, multimatrix formulation of mesalamine
        • Lialda is marketed as a once-daily treatment for ulcerative colitis
        • Lialda has been compared with Asacol in a Phase III clinical trial
        • Gastroenterologists scored Lialda well on side-effect profile
        • Lialda is perceived by gastroenterologists to perform well on patient compliance, convenient dose and convenient administration frequency
      • Asacol (mesalazine)
        • Asacol is a delayed-release formulation of mesalazine, which is marketed by Proctor & Gamble
        • Asacol well perceived on familiarity with product and availability
      • Salofalk (mesalazine)
        • Salofalk is a Eudragit-L-coated pellet formulation of mesalazine
        • Salofalk and Pentasa are equally effective in achieving remission in mild to moderate ulcerative colitis patients
        • Salofalk did not perform well on patient compliance and convenient administration frequency
      • Claversal (mesalazine)
        • Like Salofalk, Claversal is a micropellet formulation of mesalazine
      • Fivasa (mesalazine)
        • In France, Asacol is marketed as Fivasa by Norgine Pharma
      • Salazopyrin (sulfasalazine)
        • Gastroenterologists did not rate Salazopyrin well on side-effect profile
    • Biologics: brand comparison shows that Remicade remains the leader, but Humira is perceived well by physicians
      • Remicade (infliximab)
        • Gastroenterologists rate Remicade well on familiarity with product and symptomatic improvement
        • Mucosal healing is associated most with Remicade than the other biologics
        • Remicade is not associated with a convenient dose and convenient administration frequency
        • More than three-quarters of severe patients with inflammatory bowel disease receive Remicade as their first biologic therapy
        • 40% of patients who receive Remicade as their first biologic will terminate therapy
        • Most patients terminate Remicade therapy within the first year
        • An inadequate response is the most common reason for terminating Remicade therapy within the first year
        • Inadequate response remains the most common reason for terminating Remicade therapy after 1 year
        • Over a third of patients who fail Remicade therapy will move on to treatment with Humira
        • Surgery is the next step for many patients who fail Remicade therapy
        • Almost a quarter of Remicade-refractory patients progress to therapy with corticosteroids
        • Despite no evidence of efficacy in Crohn' s disease, a small percentage of Remicade-refractory patients go on to receive Enbrel (etanercept)
      • Humira (adalimumab)
        • Humira is a self-administered, fully human anti-TNF monoclonal antibody
        • Clinical trials for Humira demonstrate efficacy in biologic-naïve patients and infliximab-refractory patients with Crohn' s disease
        • Gastroenterologists scored Humira better than Remicade on a number of attributes
      • Cimzia (certolizumab pegol)
        • Cimzia is a pegylated, humanized anti-TNF therapy
        • PRECISE 1 and PRECISE 2 trials demonstrated the safety and efficacy of Cimzia, but the therapy was rejected by the FDA
        • Cimzia was rejected for Crohn' s disease in the EU in November 2007
        • Cimzia was perceived by gastroenterologists to perform well on convenient dose and administration frequency
      • Tysabri (natalizumab)
        • Tysabri prevents leukocytes migrating into the gut in Crohn' s disease
        • The EMEA' s CHMP returned a final negative opinion for Tysabri in Crohn' s disease in November 2007
        • The ENACT and ENCORE trials demonstrated the efficacy of Tysabri in Crohn' s disease
        • Tysabri was not rated well on symptomatic improvement or side-effect profile
  • BIBLIOGRAPHY
    • Journal papers
    • Websites
    • Other
  • APPENDIX A
    • Physician research methodology
      • Physician sample breakdown
      • US
      • Japan
      • France
      • Germany
      • Italy
      • Spain
      • UK
    • Contributing experts
  • APPENDIX B
    • The survey questionnaire
      • 1. Patient Segmentation
      • 2. Prescribing factors
      • 3. Treatment classes and severity
      • 4. Treatment of severe disease
  • APPENDIX C
    • About Datamonitor
      • About Datamonitor Healthcare
      • About the Immunology and Inflammation analysis team
      • Disclaimer
    • List of Tables
      • Table 1: Montreal sub-classification for Crohn' s disease, 2005
      • Table 2: Montreal classification for ulcerative colitis covering extent and anatomy, 2005
      • Table 3: Epidemiological studies into incidence and prevalence of Crohn' s disease and ulcerative colitis, 1978─2007
      • Table 4: Prevalence and incidence of Crohn' s disease in the seven major markets by country, 2007
      • Table 5: Prevalence and incidence of ulcerative colitis in the seven major markets by country, 2007
      • Table 6: Age- and sex-specific and adjusted prevalence of ulcerative colitis in Olmsted County, Minnesota, January 2001
      • Table 7: Age- and sex-specific and adjusted prevalence of Crohn' s disease in Olmsted County, Minnesota, January 2001
      • Table 8: Incidence and prevalence of Crohn' s disease and ulcerative colitis in the UK, 1995
      • Table 9: Annual prevalence and incidence of Crohn' s disease and ulcerative colitis in Japan, 1991
      • Table 10: Number of respondents reporting Crohn' s disease patients with each complication, by country, 2007
      • Table 11: Number of respondents reporting ulcerative colitis patients with each complication, by country, 2007
      • Table 12: Number and percentage of gastroenterologists prescribing each therapy at first-line for Crohn' s disease, 2007
      • Table 13: Number and percentage of gastroenterologists prescribing each therapy at first-line for ulcerative colitis, 2007
      • Table 14: Number and percentage of gastroenterologists prescribing each therapy at second-line for Crohn' s disease, 2007
      • Table 15: Number and percentage of gastroenterologists prescribing each therapy at second-line for ulcerative colitis, 2007
      • Table 16: Number and percentage of gastroenterologists prescribing each therapy at third-line for Crohn' s disease
      • Table 17: Number and percentage of gastroenterologists prescribing each therapy at third-line for ulcerative colitis
      • Table 18: Mean ranking for each reason for not using a top-down approach in severe Crohn' s disease, 2007
      • Table 19: Mean ranking for each reason for not using a top-down approach in severe ulcerative colitis, 2007
      • Table 20: Number and percentage of physicians able to rate each brand of 5-ASA
      • Table 21: Number and percentage of physicians able to rate each brand of biologic
      • Table 22: Comparison of key studies for Remicade, Humira, Cimzia and Tysabri
      • Table 23: Side effects associated with sulfasalazine and 5-ASAs
      • Table 24: Dosing schedule for the 5-ASA brands
      • Table 25: Attributes scores for each of the 5-ASA brands
      • Table 26: Attributes scores for each of the biologic brands
      • Table 27: Remicade' s attribute scores by country
      • Table 28: Percentage of patients who terminate Remicade therapy in each time period, by country
      • Table 29: Percentage of inflammatory bowel disease patients terminating Remicade therapy within the first year because of each reason, by country
      • Table 30: Percentage of inflammatory bowel disease patients terminating Remicade therapy after the first year because of each reason, by country
      • Table 31: Percentage of inflammatory bowel disease patients who fail Remicade therapy that are switched to Humira (adalimumab), by country, 2007
      • Table 32: Percentage of Remicade-refractory patients who move on to therapy with Enbrel (etanercept), by country
      • Table 33: Cimzia' s attribute scores, by country
      • Table 34: US physician sample breakdown, 2007
      • Table 35: Japan physician sample breakdown, 2007
      • Table 36: France physician sample breakdown, 2007
      • Table 37: Germany physician sample breakdown, 2007
      • Table 38: Italy physician sample breakdown, 2007
      • Table 39: Spain physician sample breakdown, 2007
      • Table 40: UK physician sample breakdown, 2007
    • List of Figures
      • Figure 1: Crohn' s disease treatment tree split by disease severity in the US, 2007
      • Figure 2: Ulcerative colitis treatment tree split by disease severity in the US, 2007
      • Figure 3: Physician-preferred first-, second- and third-line treatment regimen for Crohn' s disease in the US, 2007
      • Figure 4: Physician-preferred first-, second- and third-line treatment regimen for ulcerative colitis in the US, 2007
      • Figure 5: Crohn' s disease treatment tree split by disease severity in Japan, 2007
      • Figure 6: Ulcerative colitis treatment tree split by disease severity in Japan, 2007
      • Figure 7: Physician-preferred first-, second- and third-line treatment regimen for Crohn' s disease in Japan, 2007
      • Figure 8: Physician-preferred first-, second- and third-line treatment regimen for ulcerative colitis in Japan, 2007
      • Figure 9: Crohn' s disease treatment tree split by disease severity in France, 2007
      • Figure 10: Ulcerative colitis treatment tree split by disease severity in France, 2007
      • Figure 11: Physician-preferred first-, second- and third-line treatment regimen for Crohn' s disease in France, 2007
      • Figure 12: Physician-preferred first-, second- and third-line treatment regimen for ulcerative colitis in France, 2007
      • Figure 13: Crohn' s disease treatment tree split by disease severity in Germany, 2007
      • Figure 14: Ulcerative colitis treatment tree split by disease severity in Germany, 2007
      • Figure 15: Physician-preferred first-, second- and third-line treatment regimen for Crohn' s disease in Germany, 2007
      • Figure 16: Physician-preferred first-, second- and third-line treatment regimen for ulcerative colitis in Germany, 2007
      • Figure 17: Crohn' s disease treatment tree split by disease severity in Italy, 2007
      • Figure 18: Ulcerative colitis treatment tree split by disease severity in Italy, 2007
      • Figure 19: Physician-preferred first-, second- and third-line treatment regimen for Crohn' s disease in Italy, 2007
      • Figure 20: Physician-preferred first-, second- and third-line treatment regimen for ulcerative colitis in Italy, 2007
      • Figure 21: Crohn' s disease treatment tree split by disease severity in Spain, 2007
      • Figure 22: Ulcerative colitis treatment tree split by disease severity in Spain, 2007
      • Figure 23: Physician-preferred first-, second- and third-line treatment regimen for Crohn' s disease in Spain, 2007
      • Figure 24: Physician-preferred first-, second- and third-line treatment regimen for ulcerative colitis in Spain, 2007
      • Figure 25: Crohn' s disease treatment tree split by disease severity in the UK, 2007
      • Figure 26: Ulcerative colitis treatment tree split by disease severity in the UK, 2007
      • Figure 27: Physician-preferred first-, second- and third-line treatment regimen for Crohn' s disease in the UK, 2007
      • Figure 28: Physician-preferred first-, second- and third-line treatment regimen for ulcerative colitis in the UK, 2007
      • Figure 29: Age- and sex-adjusted incidence of Crohn' s disease and ulcerative colitis in Olmsted County, Minnesota, 1940-2000
      • Figure 30: Estimated annual prevalence and incidence rates of Crohn' s disease in Japan, 1986-1998
      • Figure 31: Diagnosed Crohn' s disease patients by severity in the seven major markets, 2007
      • Figure 32: Diagnosed ulcerative colitis patients by severity in the seven major markets, 2007
      • Figure 33: Diagnosis of inflammatory bowel disease
      • Figure 34: Crohn' s disease diagnosis rates, by country, 2007
      • Figure 35: Ulcerative colitis diagnosis rates, by country, 2007
      • Figure 36: Percentage of Crohn' s disease patients suffering from each complication, 2007
      • Figure 37: Percentage of ulcerative colitis patients suffering from each complication, 2007
      • Figure 38: Percentage of inflammatory bowel disease patients with various co-morbidities, 2007
      • Figure 39: Mean percentage of Crohn' s disease patients receiving each type of therapy by disease severity, 2007
      • Figure 40: Mean percentage of ulcerative colitis patients receiving each type of therapy by disease severity, 2007
      • Figure 41: Percentage of patients with Crohn' s disease not receiving treatment, split by disease severity, by country, 2007
      • Figure 42: Percentage of patients with ulcerative colitis not receiving treatment, split by disease severity, by country, 2007
      • Figure 43: American College of Gastroenterology: Management of Crohn' s disease in adults
      • Figure 44: Algorithm for the medical management of Crohn' s disease, 2003
      • Figure 45: American College of Gastroenterology: Ulcerative colitis practice guidelines in adults
      • Figure 46: Percentage of Crohn' s disease patients receiving antibiotics by disease severity in the seven major markets, 2007
      • Figure 47: Percentage of ulcerative colitis patients receiving antibiotics by disease severity in the seven major markets, 2007
      • Figure 48: Percentage of Crohn' s disease patients receiving anti-spasmodics by disease severity in the seven major markets, 2007
      • Figure 49: Percentage of ulcerative colitis patients receiving anti-spasmodics by disease severity in the seven major markets, 2007
      • Figure 50: Percentage of Crohn' s disease patients receiving anti-diarrheals by disease severity in the seven major markets, 2007
      • Figure 51: Percentage of ulcerative colitis patients receiving anti-diarrheals by disease severity in the seven major markets, 2007
      • Figure 52: Percentage of Crohn' s disease patients receiving oral 5-ASAs by disease severity in the seven major markets, 2007
      • Figure 53: Percentage of ulcerative colitis patients receiving oral 5-ASAs by disease severity in the seven major markets, 2007
      • Figure 54: Percentage of Crohn' s disease patients receiving topical 5-ASAs by disease severity in the seven major markets, 2007
      • Figure 55: Percentage of ulcerative colitis patients receiving topical 5-ASAs by disease severity in the seven major markets, 2007
      • Figure 56: Percentage of Crohn' s disease patients receiving corticosteroids by disease severity in the seven major markets, 2007
      • Figure 57: Percentage of ulcerative colitis patients receiving corticosteroids by disease severity in the seven major markets, 2007
      • Figure 58: Percentage of Crohn' s disease patients receiving traditional immunosuppressants by disease severity in the seven major markets, 2007
      • Figure 59: Percentage of ulcerative colitis patients receiving traditional immunosuppressants by disease severity in the seven major markets, 2007
      • Figure 60: Percentage of Crohn' s disease patients receiving biological therapy by disease severity in the seven major markets, 2007
      • Figure 61: Percentage of ulcerative colitis patients receiving biological therapy by disease severity in the seven major markets, 2007
      • Figure 62: Percentage of mild Crohn' s disease patients receiving monotherapy or combination therapy in the seven major markets, 2007
      • Figure 63: Percentage of moderate Crohn' s disease patients receiving monotherapy or combination therapy in the seven major markets, 2007
      • Figure 64: Percentage of severe Crohn' s disease patients receiving monotherapy or combination therapy in the seven major markets, 2007
      • Figure 65: Percentage of mild ulcerative colitis patients receiving monotherapy or combination therapy in the seven major markets, 2007
      • Figure 66: Percentage of moderate ulcerative colitis patients receiving monotherapy or combination therapy in the seven major markets, 2007
      • Figure 67: Percentage of severe ulcerative colitis patients receiving monotherapy or combination therapy in the seven major markets, 2007
      • Figure 68: Percentage of Crohn' s disease patients progressing from first-line to second-line treatment regimen, by country, 2007
      • Figure 69: Percentage of ulcerative colitis patients progressing from first-line to second-line treatment regimen, by country
      • Figure 70: Percentage of Crohn' s disease patients progressing from second-line to third-line treatment regimen, by country
      • Figure 71: Percentage of ulcerative colitis patients progressing from second-line to third-line treatment regimen, by country
      • Figure 72: Percentage of Crohn' s disease patients that will eventually require surgery, by country
      • Figure 73: Percentage of ulcerative colitis patients that will eventually require surgery, by country
      • Figure 74: Number of years a Crohn' s disease or ulcerative colitis patient will receive pharmacological therapy before requiring surgery, by country
      • Figure 75: Step-up versus a top-down treatment approach
      • Figure 76: Results of the first "top-down" versus "step-up" randomized controlled trial presented at the DDW 2006
      • Figure 77: Potential advantages and risks of a "top-down" treatment approach
      • Figure 78: Percentage of Crohn' s disease and ulcerative colitis patients receiving a biologic in combination with an Immunosuppressant, by country, 2007
      • Figure 79: Percentage of severe Crohn' s disease patients who receive a step-up versus a top-down treatment approach, by country, 2007
      • Figure 80: Percentage of severe ulcerative colitis patients who receive a step-up versus a top-down treatment approach, by country, 2007
      • Figure 81: Reasons, and frequency of each reason, for not using a "top-down" treatment approach in Crohn' s disease, 2007
      • Figure 82: Reasons, and frequency of each reason, for not using a "top-down" treatment approach in ulcerative colitis, 2007
      • Figure 83: Average influence on prescribing decision: weightings assigned by gastroenterologists to key attributes for 5-ASAs and biologics, 2007
      • Figure 84: Weightings for attributes in 5-ASAs and targeted biologics assigned by physicians, by country, 2007
      • Figure 85: Importance of symptomatic improvement to prescribing of 5-ASAs and biologics, by country, 2007
      • Figure 86: Importance of efficacy in promoting mucosal healing to prescribing of 5-ASAs and biologics, by country, 2007
      • Figure 87: Physicians' scores for mucosal healing and symptomatic improvement for biologic brands, 2007
      • Figure 88: Importance of speed of onset of remission to prescribing of 5-ASAs and biologics by country, 2007
      • Figure 89: Dosing schedule for biologics in Crohn' s disease
      • Figure 90: Importance of availability to prescribing of 5-ASAs and biologics by country, 2007
      • Figure 91: Importance of familiarity with product to prescribing of 5-ASAs and biologics by country, 2007
      • Figure 92: Overview brand map of attributes versus brand perception for 5-ASAs and biologics
      • Figure 93: Brand map of the marketed 5-ASAs
      • Figure 94: Brand map of the marketed and pipeline targeted biologics
      • Figure 95: Pentasa' s attribute scores
      • Figure 96: Dosing of Lialda for ulcerative colitis
      • Figure 97: Attribute scores for Lialda/Mezavant
      • Figure 98: Attribute scores for Asacol
      • Figure 99: Physician perception of the targeted biologics
      • Figure 100: Attribute scores for Remicade
      • Figure 101: Gastroenterologists' scores for mucosal healing for the biologics
      • Figure 102: Mean percentage of inflammatory bowel disease patients receiving each drug as their first biologic, 2007
      • Figure 103: Percentage of patients with inflammatory bowel disease receiving Remicade as their first biologic who will terminate therapy, by country, 2007
      • Figure 104: Percentage of patients who terminate Remicade therapy In each time period
      • Figure 105: Percentage of inflammatory bowel disease patients terminating Remicade therapy within the first year because of each reason
      • Figure 106: Percentage of inflammatory bowel disease patients who fail Remicade therapy that are switched to each of the following therapy options, 2007
      • Figure 107: Humira' s attribute scores
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