Feb 3, 2024

Clinical Research Is Just the Starting Point

Clinical Research Is
Just the Starting Point

A huge part of solving the wider healthcare challenge is making science understandable to the wider public, At the moment, we are blocking progress by making science very difficult to understand, One thing that we have been working on is a tool that translates science into easy to understand content with AI.

Livia Lifes

Livia Lifes

Neuroute vs Citeline: Fix Information Flow

Traditional players provide disconnected answers to questions that aren't related to each other, or related to you.

Over 86% of clinical trials are delayed by 6 months or more (Kim et al.,2023). 1 in 3 sites fail to recruit a single participant (Fogel,2018). The three most common trial-specific barriers to recruitment (cited by Principal Investigators) were restrictive eligibility criteria (1), complex protocols (2), and competition from nearby clinical trials (3) (Idnay et al., 2023). Historically, no one has been able to solve this problem in a meaningful way - although many have tried. There are over 500 CROs in the space and a number of vendors including Citeline or IQVIA who offer separate products for data on sites (SiteTrove), sponsors (Pharmaprojects), and studies (Trialtrove) which capture one part of the picture. Until Neuroute, there has never been a way to systematically bring every sponsor, site and study to the same place in order to map how the interactions between the specifically impact your pipeline (4).

The Solution

Use Neuroute to find out which sites have historically recruited patients with your criteria (1), de-risk complex protocols by understanding the outcomes of similar studies (2) and see all competing studies to prevent enrollment delays (3). Every single sponsor, site and study has been mapped in relation to one another, and mapped to your specific pipeline, ideas and opportunities (4).

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Jan 13, 2025

Jan 13, 2025

Jan 13, 2025

Impact of 42 CFR Part 11 on AI in Clinical Trials

42 CFR Part 11 mandates clinical trial registration and results reporting on ClinicalTrials.gov to ensure transparency. AI can automate compliance, analyze trial data for insights, and optimize patient recruitment. These regulations create opportunities for using AI platforms like Neuroute to streamline clinical trial processes and enhance efficiency.

Charles Ebaugh

Dec 12, 2024

Dec 12, 2024

Dec 12, 2024

The impact of new clinical trials regulations on AI uptake (UK, will US follow?)

The UK’s new clinical trial regulations aim to speed up approvals, improve transparency, and enhance patient involvement. Key changes include a 60-day approval timeline, mandatory trial registration and result publication, simplified consent for low-risk trials, and guidance on diversity in recruitment. Research Ethics Committees will have more flexibility, and 20 new clinical research hubs will be established. For AI, these changes create opportunities to automate compliance, optimize trial design, improve patient recruitment, and enhance data transparency, making clinical trials faster and more efficient.

Charles Ebaugh

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Turn ideas into medicine

Turn ideas into medicine

Turn ideas into medicine