Decentralized clinical trials replace physical sites with a single, virtual, central site. Patients can be recruited without regard to physical location, and are not required to visit a physicial site. Multiple investigators and site teams can be replaced by a single principle investigator and study team. Data are collected via telemedicine, electronic patient reported outcomes, and remote data capture from devices and wearables.
CRO Services
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Study Design
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IRB
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Patient Recruitment
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Consent & Enrollment
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Direct-to-Patient Logistics
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Remote Patient Engagement
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Lab Coordination
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Clinical Oversight
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Data Analytics
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Regulatory
Stratus: Curavit's DCT Platform
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Study Design
Curavit works upstream with sponsors...
Curavit works with world-class principal investigators to identify endpoints and create protocols from “first principles” to design studies that are digitally native.
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IRB Review
Curavit will manage your Institutional Review...
Curavit will manage your Institutional Review Board (IRB) process. We can work with your existing IRB or recommend an IRB for your study.
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Patient Recruitment
Utilizing novel methods and channels...
Curavit recruits participants from the 97% of potential patients who are traditionally excluded from clinical research, including ethnically and socio-economically underserved and underrepresented populations.
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Consent & Enrollment
Participants are screened, consented, enrolled, and...
Curavit screens, consents, enrolls, and engages participants through Stratus, our proprietarty DCT platform.
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Direct-to-Patient Logistics
Curavit manages all digital and physical...
Curavit coordinates all of the complex logistics - digital and physical - required to run a fully decentralized trial.
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Remote Patient Engagement
Curavit monitors patients remotely using...
Curavit's central site supports 100% remote-based monitoring of patient activity to ensure patient safety, protocol adherence, and retention.
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Lab Coordination
Curavit facilitates and manages participants' external...
Curavit facilitates and manages participants' external labs and integrates the results into Stratus, our proprietary DCT platform.
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Clinical Oversight
Curavit's supervisors ensure quality of care in...
Curavit's clinical study teams monitor trial data in real time to ensure patient safety, protocol adherence, and patient retention. This incorporates digital consent, telehealth, and remote data capture technologies.
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Data Analytics
Curavit's data management team creates the statistical...
Curavit's data management team creates the statistical plan and provides full data analysis for the final study report.
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Regulatory
Curavit's regulatory affairs scientists oversee the...
Curavit's regulatory affairs team oversees the process of getting your therapy or device through FDA review and approval and onto the market.
Curavit's DCT Platform
Decentralized clinical trials replace physical sites with a single, virtual, central site. Patients can be recruited without regard to physical location, and are not required to visit a physicial site. Multiple investigators and site teams can be replaced by a single principle investigator and study team. Data are collected via telemedicine, electronic patient reported outcomes, and remote data capture from devices and wearables.
Curavit Case Studies
Swing Therapeutics and Curavit Partner to Deploy a Virtual Site in a Decentralized Fibromyalgia Study
Swing Therapeutics, a leader in Digital Therapeutics, is working to offer people new ways to improve the management of fibromyalgia, autoimmune and chronic pain conditions with products they can use from the comfort of their home. For their pivotal study, they designed the protocol to leverage both physical clinical sites and a virtual site.
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