52% of patients who enter screening in retina trials fail to qualify.1
Ophthalmic imaging endpoints often lose almost 40% of scans to quality issues.2
Common functional endpoints have up to 50% variability.3
Ophthalmology clinical trials seem straightforward, until hidden pitfalls start impacting your data quality, timeline, and budget.
From enrollment and endpoint selection to regulatory expectations, ophthalmology trials face unique difficulties:
A surface-level approach isn't enough. To avoid costly missteps, unlock efficiencies, and pave the way for more effective ophthalmology treatments, see what others don't with IDDI.
With a 35+ year legacy and experience supporting 180+ ophthalmology trials across retinal diseases, glaucoma, rare diseases, and MedTech, IDDI is your clinical data partner.
Our biostatistics-first model is the key to successful ophthalmology clinical trials, going deeper with strategic design, superior execution, therapeutic expertise, and a laser focus on helping patients to reduce risk and improve outcomes.
References
Our one-pager takes a closer look at ophthalmology clinical trial challenges and IDDI's biostatistics-driven solutions, giving you an exclusive view of what it takes to win in this growing therapeutic area. Get your copy now to see what others don't.