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

+ Identify biggest barriers for your patient population

+ The patient-reported impact of their condition

+ Study participation vs. condition severity

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