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Ophthalmology
Optimising pharmaceutical & device development
ICON has supported success in ophthalmology drug and device development across the globe with a complete range of leading solutions and services.
Globally, one billion people have moderate or severe distance vision impairment or blindness due to unaddressed refractive error, cataract, age-related macular degeneration, glaucoma, diabetic retinopathy, as well as near vision impairment caused by unaddressed presbyopia. Aging populations mean that glaucoma alone is expected to affect more than 80 million people worldwide by 2021, potentially becoming the leading cause of blindness.
As a global, full-service CRO, ICON is a trusted partner for ophthalmic development for both medical devices and pharmaceuticals. We will work with you to maximise efficiency and value—from trial design to commercialisation and beyond.
ICON offers proven expertise, helping clients achieve success across the following ophthalmology areas:
- Age-related macular degeneration
- Cataracts
- Conjunctivitis
- Dry Eye Disease (DED)
- Glaucoma
- Macular Edema
- Myopia
- Ocular disease
- Retinal diseases
Medical Devices
Retina implant technology and digital devices are growing in importance in their contribution to the fight against blindness. For age-related conditions such as glaucoma, they can help address the challenge of poor adherence to a drug regimen.We have assisted clients in meeting FDA and other international regulatory requirements, and conducting clinical studies for numerous ophthalmic related device projects:
- Intra-corneal inlay for the treatment of presbyopia
- Non-surgical vision restoration therapy software device
- Suite of novel devices to detect macular degeneration
- Ophthalmic image processing software
- Artificial cornea
Our Services
ICON has provided operational and clinical expertise, helping clients maximise success from design to commercialisation. We work with you to:
- Optimise site selection with our trusted databases and clinical networks
- Streamline your trials with integrated research capabilities
- Maximise commercial success with competitive analysis and market expertise - our Clinical Outcomes & Assessment group has helped clients deliver compelling payer evidence through effective PRO and ClinRO strategies.
- Ensure the safety of your product using medical imaging and regulatory expertise
- Increase your product’s impact with strategic communications planning services
The following videos look at Age Related Macular Degeneration, Inherited Blindness, Diabetic Retinopathy and RhoNova™. RhoNova™ is being developed by Genable and the video was produced by FIRECREST.
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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