Gastrointestinal
ICON has experience in managing clinical studies in all major gastrointestinal indications.
Gastrointestinal
ICON has extensive experience in conducting gastrointestinal studies across the entire drug development spectrum, ranging from the initial studies in Phase I through post-marketing efforts in Phase IV. In the past five years, ICON has conducted approximately 80 clinical gastrointestinal studies, assessing over 18,500 patients at 3,600 sites worldwide.
Our clinical trial experience includes but is not limited to the following gastrointestinal indications:
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Investigative Sites
Our global investigator database includes over 1,500 gastrointestinal investigative sites across 50 countries. We have worked with a wealth of specialty investigators in the areas of Abdominal Hernias, Anal and Rectal Conditions, Benign GI Neoplasms, Infections, Inflammations, Motility, Stenosis, Ulceration and Vascular Conditions, Diverticular Disorders, Exocrine Pancreatic Disorders, GI Hemorrhages, Malabsorption, Perotineal and Retroperitoneal Conditions, Salivary Gland Conditions, Tongue Conditions, and Oral Soft Tissue Conditions.
Gastrointestinal TAG (Therapeutic Area Group)
ICON’s Gastrointestinal TAG is comprised of internal therapeutic specialists who are experienced in clinical research and drug development. The Gastrointestinal TAG contains networks with thought leaders, investigators, and clinical professionals throughout the world who are available to consult on individual projects. In addition to providing support and guidance to the study team, the main responsibilities of the TAG teams include:
- Global project feasibility
- Protocol development, review and evaluation
- Clinical trial planning
- Therapeutic training and advice
- Project oversight
- Consulting, medical monitoring and advisory board representation
- Interpretation of the clinical data
- A 24-hour, global physician “on call” system to assure that no enrollment opportunity is missed