Early clinical development planning & strategy
Creating a comprehensive development strategy requires answers to complex questions that are best served by RWD. Identify unmet medical needs within diseases/diagnoses, size market opportunities, or pinpoint gaps in today’s therapies to differentiate your asset and clinical program endpoints.
Protocol design and patient population impact
Crafting a clinical trial protocol that is scientifically rigorous and operationally feasible is no small feat. Using RWD, Citeline can analyze your protocol design iterations to show impact on eligible patient populations and help you find a balance in your eligibility that works — on paper and in real life.
Site and principal investigator selection
Select the best sites and investigators for your trial by shortlisting with those with the highest volume of potentially eligible patients for your trial — aka, protocol-matched patients — in addition to the right experience, availability, and other insights gleaned from Trialtrove and Sitetrove.
Once you’ve identified HCPs treating patients that match your protocol, tap into Citeline Connect services for outreach to support recruitment. Raise awareness about your clinical trial with HCPs who have direct, confirmed access to potential participants.
How it works
We understand that every client has unique requirements and objectives. That's why we offer fully customizable solutions that align with your specific needs. Whether you require ad-hoc data extracts, in-depth analysis and recommendations, site/investigator identification, or real-world evidence generation, we have the flexibility and resources to tailor our services to your individual goals. Our agile approach ensures that you receive actionable insights in a timely manner, empowering you to make informed decisions with confidence.