- Home
- Therapeutics
- Endocrine & Metabolic Disorders
Endocrine & Metabolic Disorders
Overcoming the unique challenges of clinical development
Running global studies in endocrine & metabolic disorders is a core competency within ICON
Our clinical trial experience includes diabetes, obesity, dyslipidemia, and metabolic syndrome.
ICON has conducted diabetes trials in all global regions and has particular experience in running studies in emerging regions such as Eastern Europe, India and South America where there are large pools of Type I and Type II diabetes patients. We have a network of offices in these regions and has developed strong relationships with investigator sites to ensure high rates of patient enrolment and retention.
Our glucose clamping techniques offer more adaptable and reproducible procedures than ever before in the development of new agents to treat Type 1 and Type 2 diabetes. Clients using ICON’s Glucose Clamping services are getting key proof of concept data 90% faster and at lower cost.
Metabolic disorders therapeutic area group
ICON has created a team of in-house global experts to support and oversee drug development programmes.
The Metabolic Disorders Therapeutic Area Group (TAG) members share a common expertise in metabolic disorders in their areas of competence: medical, laboratory, imaging operations, statistics and consulting. They provide therapeutic indication training to the project team to enable studies to get up and running soon and to meet aggressive project timelines.
TAG members are a permanent resource for the study team throughout the course of the project.
Mobile & wearable technologies
ICON is supporting the use of mobile and wearable technologies to help people with diabetes to better manage their condition.
In September 2015, ICON sponsored cyclists in the mHealth Grand Tour which delivered a world-first solution to track blood glucose levels and other key vital diabetes statistics online and in real-time. Equipped with a range of wearables which were supported by mobile technologies, the tour also gave patients new insights and information on how their condition evolved during the day.
In this section
-
Biosimilars
-
Cardiovascular
- Cell and Gene Therapies
- Central Nervous System
- Endocrine & Metabolic Disorders
- Infectious Diseases
- Internal Medicine & Immunology
-
Medical Device
- Oncology
-
Pediatrics
- Rare & Orphan Diseases
- Vaccines
-
Women's Health
-
Therapeutics insights
- Cardiovascular
- Cell and Gene Therapies
- Central Nervous System
-
Glycomics
- Infectious Diseases
- NASH
-
Women's Health Insights
-
Oncology
- Pediatrics
-
Rare and orphan diseases
-
Pushing boundaries in idiopathic pulmonary fibrosis clinical research
-
Advanced therapies for rare diseases
-
Cross-border enrollment of rare disease patients
-
Crossing the finish line: Why effective participation support strategy is critical to trial efficiency and success in rare diseases
-
Diversity, equity and inclusion in rare disease clinical trials
-
Identify and mitigate risks to rare disease clinical programmes
-
Leveraging historical data for use in rare disease trials
-
Natural history studies to improve drug development in rare diseases
-
Patient Centricity in Orphan Drug Development
-
The key to remarkable rare disease registries
-
Pushing boundaries in idiopathic pulmonary fibrosis clinical research