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CNS Neurology
Deep neurodegeneration expertise and innovative technology solutions
The prevalence and incidence of neurodegenerative diseases is projected to rise, however, there are currently no treatments to slow neurodegeneration for most diseases.
While there is a critical need to advance research, clinical trials in this field are complex and patient recruitment and retention are often a challenge.
Reducing patient burden is especially important in neurodegenerative studies. Our solutions make it convenient for the patient to complete the protocol assessments and stay engaged throughout the clinical study.
ICON In-Home and Alternate Site Clinical Solutions plus the use of telemedicine technology and FIRECREST eViewer and eConsent, allow for a most patient-friendly study set-up – in the past five years, ICON's Symphony Clinical Research has supported 57 studies in neurology with in-home clinical trial services
Accellacare, ICON's Global Site Network includes 55 CNS specialised sites across the globe with a proven track record in studies in neurodegeneration for rapid start-up, competent execution and patient access. We use these sites to evaluate the site and patient burden of a protocol prior to it being finalised.
ICON neurodegenerative and neuromuscular experience in last five years
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167
Neurodegenerative and neuromuscular clinical studies -
18,650+
neurodegenerative and neuromuscular patients and healthy volunteers (HV) -
4,200+
sites globally
Wet, imaging and digital biomarker neurology endpoints
ICON has all relevant services for wet, imaging and digital biomarker endpoints in house:
ICON Bioanalytical Laboratories support the development and analysis of biomarker assays in the neurodegenerative disease space including determination of A-B 1-42, Total tau, Phospho tau, NFL, APOE Geno, and APOE.
ICON Medical Imaging has supported 20+ studies in neurodegenerative indications and provides rigorous analysis of novel imaging endpoints and surrogate markers.
ICON provides an end-to-end approach to effective integration of wearable devices into trial design, execution and reporting. Our digital health technology team has experience developing such frameworks - from device selection to endpoint generation and operational management.
Cell and gene therapies for neurodegenerative diseases
Clinical gene therapy has emerged as an innovative therapeutic strategy for a wide range of neurodegenerative disorders, including Alzheimer’s disease, Parkinson’s disease, and rare diseases such as Huntington’s disease or Amyotrophic lateral sclerosis. ICON has a deep understanding of the specific regulatory, clinical and operational challenges of Cell and Gene Therapy clinical trials having conducted 135 such studies, including 3 very recently in the neurodegenerative space.
CNS, pain and ageing related disorders insights
ICON's experienced neuroscience and drug development teams regularly share their insights in industry publications and through ICON produced content in the form of blogs and whitepapers. Read more content from our experts.
In this section
- Biosimilars
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Cardiovascular
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Medical Device
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Pediatrics
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Women's Health
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Therapeutics insights
- Cardiovascular
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Glycomics
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Women's Health Insights
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Oncology
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Rare and orphan diseases
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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