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Inflammatory Bowel Disease (IBD)
Offering a broad range of support from initial strategy development all the way through to pricing and market access recommendations
Inflammatory Bowel Disease (IBD) is a chronic, relapsing, inflammatory disorder of the gastrointestinal tract and includes Ulcerative Colitis (UC) and Crohn’s Disease (CD).
IBD affects over 5 million people worldwide, and the incidence has been growing steadily over the past 10 years.
While the exact cause of IBD is unknown, the inflammation results from the immune system’s response to environmental triggers. Today, the goal of treatment is to bring about and maintain remission, and a range of advanced treatment options are available to reduce inflammation and manage symptoms. The area is one of the most active in biopharmaceutical development and clinical research with hundreds of active trials in progress.
ICON IBD experience in the last five years
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43
Studies conducted -
20,000
Patients involved -
5,700
Sites worldwide
ICON offers end-to-end services to support the development of your product to treat Inflammatory Bowel Disease. In the past seven years, we’ve conducted over 15 studies in Crohn’s disease and over 35 in Ulcerative Colitis, giving us a profound understanding of the clinical and operational challenges in this therapeutic area. Such immersion translates into strong development plans, efficient study management, defensible data packages, and careful preparation for commercial success.
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Pushing boundaries in idiopathic pulmonary fibrosis clinical research
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Advanced therapies for rare diseases
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Cross-border enrollment of rare disease patients
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Crossing the finish line: Why effective participation support strategy is critical to trial efficiency and success in rare diseases
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Diversity, equity and inclusion in rare disease clinical trials
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Identify and mitigate risks to rare disease clinical programmes
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Leveraging historical data for use in rare disease trials
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Natural history studies to improve drug development in rare diseases
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Patient Centricity in Orphan Drug Development
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The key to remarkable rare disease registries
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Pushing boundaries in idiopathic pulmonary fibrosis clinical research