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Navigating Clinical Trials in the Coronavirus Era

LOS ANGELES, March 12, 2020
Navigating Clinical Trials in the Coronavirus Era

Science 37, the industry leader in decentralized clinical trials, today published a report examining key considerations for patient safety and business continuity in the clinical trial industry in light of the current COVID-19 pandemic. 

The impact of COVID-19 is immense and well documented in the context of global health, but the impact to clinical research, trial sponsors, research investigators and trial participants has gone virtually untold. At any given moment, there are more than 40,000 ongoing global clinical trials, involving thousands of trial sites, tens of thousands of investigators, and hundreds of thousands of patients. The whitepaper, Navigating Clinical Trials in the Coronavirus Era, details steps that pharmaceutical companies might take to mitigate risks to ongoing trials.

“We are seeing a significant and growing number of cases where clinical trial participants are refusing to visit hospitals or local clinics for fear that they could be exposed to COVID-19,” says Jonathan Cotliar, chief medical officer of Science 37. “By all accounts, we expect this issue to continue to compound over time, which makes risk-mitigation strategies an imperative to protect the safety and well-being of participants and to enable business continuity.”

At the heart of Science 37’s recommendations is to incorporate telemedicine investigators and at-home nurse visits to replace clinic visits. The majority of all clinical trial visits can be conducted remotely with the help of today’s technology and network of investigators who are trained to manage both the technology and the participant relationships. In addition, mobile research nurses, taking all CDC-recommended precautionary measures, can be deployed to visit participants at home to collect blood and biospecimens, monitor vital signs, complete protocol-specified procedures and capture data through the use of a virtual trial platform. 

Beyond the need for risk-mitigation, many patients prefer remote investigator visits and one-on-one home visits with a healthcare professional rather than having to travel to a research site or even a local lab for a blood draw. 

For clinical trials that are currently in flight, FDA regulations allow for expedited changes when submitting amendments to IRBs that relate to immediate hazards to participants. For future trials, sponsors now must design their trials with these risk-mitigation strategies already in mind. 

The report describes key considerations for virtualizing protocols to minimize in-person interactions to maintain public health, particularly for those who are most vulnerable.

About Science 37

Science 37 is making the promise of virtual trials the new reality. By engaging with patients from the comfort of their own home, we provide access to patients who can never be reached by traditional site-based models. We have proven to enroll faster, retain patients at a higher rate, and reach a more representative population. Science 37 has conducted more decentralized, interventional trials than any other company, using an expansive, in-house network of telemedicine investigators and home-health nurses, who are supported by the industry’s most comprehensive, fully-integrated, decentralized clinical trial platform. Learn more at Science 37, and follow Science 37 on TwitterLinkedIn, and Facebook.

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