Studies leveraging patient insights, recruit 30% more patients
Our feasibility insights help you avoid delays, costly amendments and enrollment barriers
Studies leveraging patient insights, recruit 30% more patients
Our feasibility insights help you avoid delays, costly amendments and enrollment barriers
Patient and site insights designed to improve your study’s recruitment
We gather insights directly from patients and HCPs across the globe, provide our key findings, and organize the data in our Clinlytics platform.
These insights answer the questions your study team should be asking:
- How does your study’s target population vary by country, ethnicity, and more?
- What is the trade-off between your I/E requirements and patient willingness to participate?
- Do your chosen sites have the right patients, technology, and staff to support your study?
Our insights identify avoidable costs & delays
By identifying recruitment barriers, optimizing protocols, and selecting the most appropriate sites, we enable sponsors to conduct more efficient, patient-centric clinical trials.
57%
of all protocols require at least one substantial amendment
$535K
is the average cost per
protocol amendment
$600K – 8M
is the cost per day in lost sales due to study delays
Insights aligned to your focus areas
If you’re seeking to enhance your understanding of the target patient population, refine site selection, optimize protocols, or explore important focus topics such as clinical trial diversity, we can support you and your study.
Patient focus
+ Identify biggest barriers for your patient population
+ The patient-reported impact of their condition
+ Study participation vs. condition severity
Geography focus
+ Choose sites with the right staff & patients
+ Which countries host your target population
+ Identify site locations with more diverse patient pools
Topic focus
+ Design a study that boosts diversity, equity, & inclusion
+ Learn how DCT can benefit your studies
+ Create new study evaluation processes
Protocol focus
+ Pre-empt expensive protocol amendments
+ Know which procedures are truly required
+ Have patient feedback on your I/E criteria
Study feasibility
Why choose Clariness for feasibility?
Design more
patient-centric studies
We enable co-creation, by getting patient feedback on your
study’s design
Medical experts &
trained psychiatrists
We have trained experts that develop our feasibility surveys, to uncover impactful insights
Feasibility & performance data from 1,200 studies
We leverage feasibility data from 18+ years of supporting studies across 100+ indications
Pre-identify
costly amendments
Avoid costly protocol amendments by identifying recruitment barriers early
Pre-populate
your patient funnel
We match survey respondents with your protocol, to pre-populate your patient funnel
Contact us to find out how we can accelerate your clinical trials
Chat with one of our experts today for personalized solutions and support