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June 24, 2020updated 12 Jul 2022 11:44am

Trialbee and Datavant to partner for clinical trial recruitment

Global technology provider Trialbee has announced a partnership with Datavant to power patient-centric clinical trial recruitment and engagement.

Global technology provider Trialbee has announced a partnership with Datavant to power patient-centric clinical trial recruitment and engagement.

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Under the partnership, Trialbee will power its clinical trial recruitment and patient engagement solutions using Datavant’s open data ecosystem.

De-identified data will be analysed to determine the characteristics of patients who may be eligible and motivated to participate in a clinical trial.

Trialbee CEO Lollo Eriksson said: “We are solving for the investigator fatigue and demotivation caused by unguided mega screening for patient recruitment and the low results it produces.

“This partnership with Datavant will significantly expand our access to real-world data (RWD) and ability to choose the information assets that are most relevant for any given trial.

“This unique collaboration will improve specificity and drive the right patients to clinical trials, improving efficiency and time to last patient enrolled.”

Trialbee is a global patient recruitment and engagement company with integrated patient sourcing using RWD from claims data, electronic health records data, as well as digital outreach to the general public.

Datavant CEO Travis May said: “Trialbee is tackling a critical problem with a fresh perspective: how to more effectively recruit patients to clinical trials and keep them engaged once they are enrolled.

“We are thrilled for the partnership to support their access to real-world data sources across Datavant’s open data ecosystem.”

In October last year, Trialbee partnered with health research network TriNetX for data-driven digital solutions to accelerate patient-centric clinical trials. Trialbee offers software to cut trial recruitment timelines and improve the patient engagement experience.

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As the industry strengthens its focus on patient centricity, Direct-to-Patient clinical trials have emerged as a popular trial design that have the potential to increase patient recruitment and retention. IRT plays a crucial role in the success of a Direct-to-Patient trial. Because drug supplies are being managed and shipped from distribution facilities directly to patients’ homes, a sponsor must have a high-quality system in place to accurately track the chain of custody, ensure patient-blinding and handle other logistical challenges. What You Will Learn Benefits and challenges associated with the Direct-to-Patient model Bellerophon's top considerations when implementing this trial design How IRT can equip study teams to successfully track chain of custody, ensure patient blinding, and handle logistical challenges
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Enter your details here to receive your free Case Study.

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