Rare disease
Maximize every moment and data point with Prelude’s flexible study builder, built-in compliance tools, and hands-on support.
Connect with an expertHow we help power rare disease research
Rare disease trials are complicated by nature with small populations, multi-site coordination, and unpredictable patient journeys. At Prelude, our mission is to simplify complex trials. With superior site experience, highly configurable study builds, and full visibility and auditing capabilities, you can access insights faster to power the next generation of breakthrough treatments.
The problem
With small patient populations, there’s no room for error. One delay or dropout can threaten your entire trial.
Our solution
Improve the patient experience with participant-friendly tools like mobile ePRO, eConsent, and automated reminders.
The problem
Rare disease trials often require custom protocols, multi-site management, and mid-study adjustments, which can cause delays or errors.
Our solution
Adapt quickly and easily with a no-code builder and protocol amendment version controls that make changes mid-study and support site-specific versions without downtime or rebuilds.
The problem
High variability across sites and visits makes consistent data capture and review a challenge, especially for hybrid or remote studies.
Our solution
Standardize data collection with reusable forms, cross-form edit checks, and dashboards that give your team visibility across every data point.
Powerful features for rare disease research
Rare disease research often takes teams through uncharted territory. With flexible tools designed to manage even the most complex protocols, you can keep sites and patients engaged and stay compliant from day one.
Highly configurable system
Adapt to any protocol with drag-and-drop forms, cross-form edit checks and calculations, and mid-study updates that don’t require rebuilds or migrations.
Remote eConsent and ePRO
Let participants sign consent forms and submit patient-reported outcomes from anywhere, using their own devices.
Clear compliance
From eSignatures to protocol versioning, track every update, entry, and query so your data stays clean, consistent, and audit-ready.
What our clients say about us
“The product is very easy to use. The software is user friendly providing real time data to the clinical study.”
Lisa Director Systems and Project Management“It's intuitive and easy to use for both the sponsor employees and the study site personnel.”
Tennery C. Clinical Operations Manager“The entire team from coordinators at the sites to managers and data analysts at the coordinating center have nothing but positive things to say about the system and its ease of use.”
Verified Program Administrator“I am also impressed by their excellent customer support and willingness to learn customers' needs.”
Ying Senior Programmer Analyst, Lead Data ManagerHow we empower rare disease teams
With small cohorts and high stakes, rare disease research teams need tools that simplify their processes and amplify their impact. Prelude empowers your team to work more efficiently and focus on the research.
Configurable studies for any protocol
No two rare disease protocols look the same. Tailor every form to your study with our configurable no-code study builder, cross-form edit checks, and advanced calculations.
Built-in visibility and site collaboration
Keep teams aligned with an easy-to-navigate interface and real-time visibility into enrollment, form status, queries, and participant-reported data.
Integrated modules for faster workflows
Run your entire trial from one place. Prelude’s platform includes EDC, ePRO, eConsent, and RTSM. Plus, use our API to integrate with your current tools.
Human-centric customer service
Partner with a dedicated Customer Success Engineer who understands complex research, knows your study inside and out, and offers hands-on support.
Related products and services
Prelude gives you everything you need to run smarter rare disease trials. Explore powerful solutions for seamless studies.
