Oncology
Adapt to complex protocols, stay organized across long timelines, and manage evolving patient pathways with a platform built for complex oncology trials.
Connect with an expertHow we power oncology research
Oncology trials are complicated, intricate, and high-stakes. With adaptive protocols across multiple phases and geographies, you need tools you can trust. Prelude’s highly configurable EDC, site- and patient-friendly interface, and in-house customer support help oncology research teams build, launch, and manage complex studies.
The problem
Oncology protocols can change fast. With multiple study arms, adjusted dose levels, unscheduled visits, and mid-study updates, it's challenging to adapt while maintaining data integrity.
Our solution
Our highly configurable system is designed for multiple cohorts, adaptive protocols, mid-study updates, and complex scheduling.
The problem
Study builders don’t always have the deep protocol knowledge of the clinical operators, which can lead to operational friction and unintuitive study design.
Our solution
Our dedicated customer success team is made up of product experts who go deep into each protocol to ensure an optimized and intuitive study build.
The problem
Tracking long-term patient outcomes and adverse events across multiple sites can be difficult and time-consuming, especially in global studies.
Our solution
Standardize consistent, compliant data capture across sites with an intuitive EDC and smart edit check features that sites love.
Powerful features for oncology research
With frequent protocol changes, multiple treatment arms, and long timelines, you need tools that flex with you. Prelude gives oncology teams the control, visibility, and scalability they need.
Drag-and-drop form builder
Quickly build eCRFs for complex oncology protocols with no-code cross-form edit checks and advanced calculations.
Flexible visit schedules and dosing updates
Adjust visit schedules and update dosing regimens on the fly to accommodate patient-specific needs and accurate data tracking.
On-demand reporting and data insights
Stay up-to-date on interim trial results with built-in reporting, query summaries, and easy exports for further analysis.
Integrated ePRO and eConsent
Collect digital consent and re-consent with custom fields and multimedia uploads. Then, send auto-reminders and collect real-time data with the mobile ePRO app – no extra office visits or paper forms required.
Seamless mid-study updates
Speed up protocol amendments with a testing database and version controls to manage updates and validations without migrations or downtime.
What our clients say about us
“It is a one-stop shop product for clinical trials management.”
Malathi Associate Scientist“Prelude EDC is very user-friendly, both for the builders creating the forms, and the users completing the forms. Staff using the forms in our study have been very positive about the experience. Highly customizable forms can be made with the building tool, and the on-form calculations, conditional fields and error checks are very helpful to prevent data entry errors.”
Verified User in Research“Incredible EDC with unparalleled versatility and customizability!”
Verified Reviewer, Program Administrator“User-Friendly EDC System and Excellent Customer Support”
Verified User in ResearchHow we empower oncology teams
We help research teams stay agile and responsive with flexible study design tools, patient-centric data collection, and support from real people who are as passionate about your study as you are.
Custom workflows for complex protocols
Have our team of product experts build for you, or use our no-code builder to support custom workflows, cross-form edit checks, and calculations that perfectly match your database design to your protocol.
Real-time reporting and monitoring
Track enrollment, site activity, and subject data across forms in real time. With intuitive dashboards and built-in query management tools, you’ll always have a bird’s eye view of your progress.
Remote-friendly patient tools
Collect patient-reported outcomes and informed consent data digitally. Prelude’s mobile ePRO and eConsent tools keep participants engaged without burdening sites or patients.
Seamless mid-study updates
Amendments are inevitable in oncology research. Make fast updates to forms mid-study with full audit trails and protocol version controls – no downtime or migration required.
Related products and services
Prelude includes everything you need to run smarter oncology trials. Explore powerful solutions for seamless studies.
