Bite Size Demo 8 - Lokavant

Start planning your clinical trial effortlessly by dragging and dropping your protocol into Lokavant’s Clinical Trial Intelligence platform. Lokavant’s AI enabled Prizm ™ CDH will autonomously extract key trial criteria and find similar historical studies to then leverage real-world data to create enrollment forecasts, patient profiles, and optimize study scenarios for your research and development strategy. Consider various scenarios and optimize your study based upon country and site mix, FPI/LPI timelines, and cost constraints.

Forecast and identify optimal sites and countries for trial success to iteratively refine study feasibility in a matter of minutes.

As your trial moves from planning to execution, input these same models to then monitor launch activities in real-time and optimize your patient recruitment and site startups to ensure trial success within an 85% confidence interval.

After your trial is successfully running and achieving enrollment milestones, concentrate on Study Oversight. Utilizing Lokavant’s Prizm CDH as your trials single source of truth you can monitor your clinical trial performance, compliance, and real-time risks, ensuring a successful study outcome.