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Accelerate trials and improve patients' lives
Find more patients, in less time, with fewer screen fails and fewer protocol amendments. Deploy AI biomarkers and search algorithms to boost the speed and accuracy of clinical trials by tapping into clinical data at its source and at scale, without data sharing. No code required.
80% of trials don't meet recruitment targets and timelines
When it comes to clinical trials, time is of the essence. Yet 80% of trials do not meet their recruitment targets on time, and 50% of sites enrol 1 or fewer patients. Current processes are slow, expensive and error-prone.
There's now a better way.
Get compounding benefits throughout the trial lifecycle
Patient pre-screening
Help trial sites identify patients meeting inclusion/exclusion criteria by using Bitfount to send algorithms and AI models to the data within their routine-care systems. Increase site yield, accelerate recruitment, and reduce screening failure rates.
- Analyse both imaging and EHR data
- Deploy premium AI biomarkers or bring your own
- Eliminate privacy risks: No data leaves the trial site
- Easy to deploy: from large hospitals to small clinics
Better patient targeting is estimated to reduce a new treatment's time to market by 1.7 years. Let's start today.
- Trial sites: Download the desktop app to get started ->
- Trial sponsors: Create an account and set up a project ->
- ML model developers: Install the SDK ->
Site selection
Make faster, more informed site selection decisions based on objective data about the patient populations accessible via each site. No more relying on over-optimistic estimates of patient availability. Optimise overall site portfolio for volume, velocity, variety or any combination of the three.
Protocol design
Optimise the design of your trial to maximise its chances of success and minimise the need for time-consuming protocol amendments. Safely simulate and iterate different sets of inclusion/exclusion criteria to ensure both clinical needs and recruitment targets can be met.
Trial feasibility studies
Before proceeding with a trial, federated data science can be used to inform feasibility studies by collecting data on patient demographics, disease prevalence, current treatments and more by partnering with trial sites to share insights from their data, without requiring them to share any of it.
Get started
Take your clinical trials to the next level.
Get started or book a demo to learn more.
Key features for clinical trials
Desktop application
Easy to deploy via a powerful and user-friendly desktop application for clinics without coding expertise. Available for Windows and Mac.
Built-in privacy preservation
No need for a PhD in cryptography. Remove risk barriers to opening up sensitive data by combining any of a range of built-in privacy-enhancing technologies (PETs).
Usage-based access controls
Partners are only able to carry out the analyses you have allowed them to. Role-based access controls let you technically enforce governance and usage policies.
Audit and monitoring
Bitfount provides a real-time, granular audit trail of how partners or consortia members use your data.
Simple IT integration
Bitfount's communication model only requires that data custodians and data scientists have outgoing internet connections. No need to open any ports in the firewall, dramatically simplifying IT integration.
End-to-end encryption
Bitfount itself never receives data or statistics. Any analysis results are transferred between data custodians and data scientists using end-to-end encryption.
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